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    <title>LabCanvas blog</title>
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    <description>Guides for scientific figures, presentations, structures and data.</description>
    <language>en</language>
    <lastBuildDate>Mon, 19 Oct 2026 09:00:00 GMT</lastBuildDate>
    <item>
      <title>ImageJ vs LabCanvas Image Analysis: an honest comparison</title>
      <link>https://www.labcanvas.com/blog/imagej-vs-labcanvas</link>
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      <pubDate>Sun, 08 Nov 2026 09:00:00 GMT</pubDate>
      <description>ImageJ/Fiji or LabCanvas Image Analysis? Six everyday jobs done in both, six newer ones (macros, vendor files, 3D, StarDist, big images) and which to use.</description>
      <category>ImageJ vs LabCanvas</category>
      <category>ImageJ alternative</category>
      <category>ImageJ online</category>
      <category>Fiji</category>
      <category>ImageJ</category>
      <category>count cells online</category>
      <category>western blot densitometry</category>
      <category>nanoparticle size distribution</category>
      <category>colocalization</category>
      <category>CTCF</category>
      <category>scale bar</category>
      <category>ImageJ macro</category>
      <category>StarDist</category>
      <category>3D object analysis</category>
      <category>deconvolution</category>
      <category>image stitching</category>
      <category>whole slide image</category>
      <category>image analysis software comparison</category>
    </item>
    <item>
      <title>LabCanvas Image Analysis: measure microscopy images, western blots and gels in your browser</title>
      <link>https://www.labcanvas.com/blog/image-analysis-microscopy-western-blot</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>How to measure images in LabCanvas Image Analysis: guided assays (nuclear translocation, spots per cell, wound healing, FRAP, calcium, tracking, branching), western blots with a ladder and total-protein normalisation, cell counting with a trainable classifier, ROIs with ImageJ definitions, on the raw pixel values, with results sent to Graphs.</description>
      <category>image analysis</category>
      <category>ImageJ alternative</category>
      <category>Fiji alternative</category>
      <category>western blot quantification</category>
      <category>cell counting</category>
      <category>nuclear translocation</category>
      <category>wound healing assay</category>
      <category>FRAP</category>
      <category>particle tracking</category>
      <category>microscopy</category>
    </item>
    <item>
      <title>Image Analysis in LabCanvas: a complete guide to every tool and setting, with examples</title>
      <link>https://www.labcanvas.com/blog/image-analysis-complete-guide</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Every tool in LabCanvas Image Analysis, tab by tab, with its settings and a real example: image check, display and scale, stacks and Z projection, background subtraction, filters, thresholds and binary operations, ROIs and Set measurements, Analyze Particles, a pixel classifier, spots, cell counter, western blot densitometry, colocalisation, colour deconvolution and eleven guided assays.</description>
      <category>image analysis</category>
      <category>microscopy</category>
      <category>ROI manager</category>
      <category>analyze particles</category>
      <category>western blot quantification</category>
      <category>colocalisation</category>
      <category>colour deconvolution</category>
      <category>Z projection</category>
      <category>cell counting</category>
      <category>FRAP</category>
      <category>particle tracking</category>
      <category>Sholl analysis</category>
    </item>
    <item>
      <title>How to use ImageJ: a beginner&apos;s tutorial for the 10 everyday jobs (2026)</title>
      <link>https://www.labcanvas.com/blog/how-to-use-imagej</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>How to use ImageJ and Fiji: get started, open an image, then 10 everyday jobs (scale, measure, threshold, count, background, blots) with exact menu paths.</description>
      <category>how to use ImageJ</category>
      <category>ImageJ tutorial</category>
      <category>how to use Fiji</category>
      <category>Fiji tutorial</category>
      <category>what is ImageJ</category>
      <category>ImageJ manual</category>
      <category>image analysis</category>
      <category>microscopy</category>
      <category>cell counting</category>
      <category>western blot quantification</category>
      <category>ImageJ alternative</category>
    </item>
    <item>
      <title>How to set the scale and add a scale bar in ImageJ (with a calibration image to practise on)</title>
      <link>https://www.labcanvas.com/blog/imagej-scale-bar-set-scale</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-scale-bar-set-scale</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Set the scale in ImageJ (Analyze › Set Scale) from a micrometer, scale bar or pixel size, add a scale bar, and practise on a free calibration image.</description>
      <category>how to add scale bar in ImageJ</category>
      <category>ImageJ scale bar</category>
      <category>set scale ImageJ</category>
      <category>calibration image for ImageJ</category>
      <category>stage micrometer</category>
      <category>pixels to micrometers</category>
      <category>pixel size</category>
      <category>spatial calibration</category>
      <category>Fiji</category>
      <category>scale bar</category>
    </item>
    <item>
      <title>Western blot quantification in ImageJ, step by step (and the 3-click way)</title>
      <link>https://www.labcanvas.com/blog/western-blot-quantification-imagej</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Quantify a western blot in ImageJ with Analyze › Gels, normalise to a loading control or total protein, and get fold change. Plus a 3-click way.</description>
      <category>western blot quantification</category>
      <category>ImageJ western blot quantification</category>
      <category>western blot analysis ImageJ</category>
      <category>densitometry ImageJ</category>
      <category>ImageJ gel analysis</category>
      <category>band intensity</category>
      <category>loading control</category>
      <category>total protein normalisation</category>
      <category>relative density</category>
      <category>fold change</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>How to count cells in ImageJ (automatic and manual)</title>
      <link>https://www.labcanvas.com/blog/count-cells-imagej</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Count cells in ImageJ: automatic (threshold, Watershed, Analyze Particles) or manual (Cell Counter, Multi-point), plus cells per mm² and % positive.</description>
      <category>ImageJ cell counting</category>
      <category>how to count cells in ImageJ</category>
      <category>Cell Counter plugin</category>
      <category>automated cell counting</category>
      <category>count nuclei</category>
      <category>Analyze Particles</category>
      <category>threshold</category>
      <category>watershed</category>
      <category>Fiji</category>
      <category>cells per mm²</category>
      <category>percent positive</category>
    </item>
    <item>
      <title>How to measure length and area in ImageJ (with the right units)</title>
      <link>https://www.labcanvas.com/blog/measure-length-area-imagej</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Measure length and area in ImageJ: set the scale, draw lines or area selections (polygon, wand, threshold), press Measure, and get µm and µm², not pixels.</description>
      <category>ImageJ length measurement</category>
      <category>how to use ImageJ to measure length</category>
      <category>ImageJ area measurement</category>
      <category>how to measure area in ImageJ</category>
      <category>ImageJ measurements</category>
      <category>Set Measurements</category>
      <category>segmented line</category>
      <category>wand tool</category>
      <category>pixels to µm</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>Grain size analysis in ImageJ (SEM, ASTM E112) + grain size number calculator</title>
      <link>https://www.labcanvas.com/blog/grain-size-analysis-sem</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Measure grain size from SEM images in ImageJ: closed boundaries, Analyze Particles, then ASTM E112 G from mean area or intercept, with a worked example.</description>
      <category>ImageJ grain size</category>
      <category>grain size analysis ImageJ</category>
      <category>ASTM E112</category>
      <category>grain size number calculator</category>
      <category>ASTM E112 calculator</category>
      <category>intercept method grain size</category>
      <category>planimetric method</category>
      <category>SEM image analysis</category>
      <category>thin film grain size</category>
      <category>perovskite film</category>
      <category>analyze particles</category>
      <category>equivalent diameter</category>
    </item>
    <item>
      <title>How to measure leaf area with ImageJ (or from a phone photo, in the browser)</title>
      <link>https://www.labcanvas.com/blog/leaf-area-imagej</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/leaf-area-imagej</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Measure leaf area in ImageJ from a photo or scan: set the scale from a ruler, threshold the leaf, run Analyze Particles in cm², with or without holes.</description>
      <category>ImageJ leaf area</category>
      <category>leaf area ImageJ</category>
      <category>how to measure leaf area from a photo</category>
      <category>leaf area measurement</category>
      <category>ImageJ leaf</category>
      <category>Analyze Particles</category>
      <category>Color Threshold</category>
      <category>insect damage</category>
      <category>set scale from a ruler</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>ImageJ online: can you run it in a browser? (ImageJ.JS, and a faster way)</title>
      <link>https://www.labcanvas.com/blog/imagej-online</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-online</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Yes: ImageJ.JS runs ImageJ 1.x in your browser via CheerpJ (WebAssembly). What works, what doesn&apos;t, Fiji online, iPad and Android, and a faster option.</description>
      <category>ImageJ online</category>
      <category>ImageJ.JS</category>
      <category>ImageJ JavaScript</category>
      <category>ImageJ JS</category>
      <category>ImageJ browser</category>
      <category>ImageJ web version</category>
      <category>Fiji online</category>
      <category>ImageJ iPad</category>
      <category>ImageJ Android</category>
      <category>CheerpJ</category>
      <category>ImJoy</category>
      <category>ImageJ alternative</category>
    </item>
    <item>
      <title>Best ImageJ alternatives in 2026 (free, online and desktop)</title>
      <link>https://www.labcanvas.com/blog/imagej-alternatives</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>The best ImageJ alternatives compared: browser tools, Fiji, CellProfiler, QuPath, ilastik, napari, Icy, MIPAR, and Image Lab and Empiria for blots.</description>
      <category>ImageJ alternative</category>
      <category>ImageJ alternatives</category>
      <category>Fiji alternative</category>
      <category>software like ImageJ</category>
      <category>best image analysis software</category>
      <category>free image analysis software</category>
      <category>microscopy image analysis</category>
      <category>CellProfiler</category>
      <category>QuPath</category>
      <category>ilastik</category>
      <category>napari</category>
      <category>western blot software</category>
    </item>
    <item>
      <title>Lateral size of 2D flakes (graphene, MoS₂) from SEM or TEM in ImageJ</title>
      <link>https://www.labcanvas.com/blog/2d-flake-lateral-size</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/2d-flake-lateral-size</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Measure graphene or MoS₂ flake lateral size in ImageJ: scale, threshold, Analyze Particles with Feret diameter, edge flakes, overlaps and a size histogram.</description>
      <category>flake size distribution</category>
      <category>graphene flake size SEM</category>
      <category>lateral size MoS2</category>
      <category>2D material flake size ImageJ</category>
      <category>Feret diameter</category>
      <category>Analyze Particles</category>
      <category>nanosheet size</category>
      <category>SEM image analysis</category>
      <category>TEM image analysis</category>
      <category>size histogram</category>
      <category>ImageJ</category>
    </item>
    <item>
      <title>Analyze Particles in ImageJ, explained (every option, with examples)</title>
      <link>https://www.labcanvas.com/blog/analyze-particles-imagej</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/analyze-particles-imagej</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Every Analyze Particles option in ImageJ, shown on a TEM image: size, circularity, Show, Exclude on edges, Include holes, and why it finds 0 or 1 particle.</description>
      <category>analyze particles ImageJ</category>
      <category>ImageJ particle analysis</category>
      <category>count particles ImageJ</category>
      <category>ImageJ particle size analysis</category>
      <category>size distribution ImageJ</category>
      <category>exclude on edges</category>
      <category>include holes</category>
      <category>circularity</category>
      <category>TEM nanoparticles</category>
      <category>watershed</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>Calcium imaging analysis in ImageJ: ΔF/F₀ traces step by step</title>
      <link>https://www.labcanvas.com/blog/calcium-imaging-delta-f-over-f</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/calcium-imaging-delta-f-over-f</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Calcium imaging in ImageJ: ROIs on cells, Multi Measure, background, F₀ (first frames or a percentile), ΔF/F₀ = (F − F₀)/F₀, traces and peak counting.</description>
      <category>calcium imaging analysis imagej</category>
      <category>delta f over f calculation</category>
      <category>df/f0</category>
      <category>ΔF/F₀</category>
      <category>GCaMP</category>
      <category>calcium transients</category>
      <category>Plot Z-axis Profile</category>
      <category>Multi Measure</category>
      <category>baseline F0</category>
      <category>peak detection</category>
      <category>ROI Manager</category>
    </item>
    <item>
      <title>CellProfiler vs QuPath vs ImageJ: which image analysis software should you use?</title>
      <link>https://www.labcanvas.com/blog/cellprofiler-vs-qupath-vs-imagej</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/cellprofiler-vs-qupath-vs-imagej</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>CellProfiler, QuPath or ImageJ/Fiji? A fair comparison by job (batch cell measurements, whole slides, general analysis), with a nuclei count step by step.</description>
      <category>CellProfiler vs ImageJ</category>
      <category>QuPath vs ImageJ</category>
      <category>best cell image analysis software</category>
      <category>CellProfiler</category>
      <category>QuPath</category>
      <category>Fiji</category>
      <category>ImageJ</category>
      <category>nuclei counting</category>
      <category>digital pathology</category>
      <category>high-content screening</category>
      <category>bioimage analysis software</category>
    </item>
    <item>
      <title>Colocalization analysis in ImageJ: Pearson vs Manders and Costes thresholds</title>
      <link>https://www.labcanvas.com/blog/colocalization-analysis-pearson-manders</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/colocalization-analysis-pearson-manders</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Colocalization in ImageJ and Fiji: what Pearson’s r and Manders’ M1/M2 each answer, Costes thresholds, Coloc 2 vs JACoP, a worked example and pitfalls.</description>
      <category>colocalization ImageJ</category>
      <category>ImageJ colocalization</category>
      <category>JACoP ImageJ</category>
      <category>Coloc 2</category>
      <category>colocalization plugin</category>
      <category>Pearson vs Manders</category>
      <category>Pearson&apos;s correlation coefficient</category>
      <category>Manders&apos; coefficients</category>
      <category>Costes threshold</category>
      <category>Fiji</category>
      <category>fluorescence microscopy</category>
    </item>
    <item>
      <title>Count bacterial colonies in ImageJ (or from a plate photo, free online)</title>
      <link>https://www.labcanvas.com/blog/colony-counter-online</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/colony-counter-online</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Count colonies in ImageJ: oval on the dish, threshold, Watershed, Analyze Particles. Then CFU/mL from the count and dilution, with a worked example.</description>
      <category>ImageJ colony counting</category>
      <category>colony counter ImageJ</category>
      <category>count colonies ImageJ</category>
      <category>colony counter online</category>
      <category>CFU counter</category>
      <category>CFU/mL calculation</category>
      <category>plate count</category>
      <category>Analyze Particles</category>
      <category>watershed</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>Measure contact angle from a drop photo in ImageJ</title>
      <link>https://www.labcanvas.com/blog/contact-angle-imagej</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/contact-angle-imagej</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Measure contact angle in ImageJ with the Angle tool along the tangent, or from drop height and base width: θ = 2·arctan(2h/d). Worked example, plugins.</description>
      <category>contact angle ImageJ</category>
      <category>ImageJ contact angle plugin</category>
      <category>drop analysis ImageJ</category>
      <category>sessile drop</category>
      <category>DropSnake</category>
      <category>LB-ADSA</category>
      <category>spherical cap</category>
      <category>wettability</category>
      <category>Bond number</category>
      <category>surface energy</category>
    </item>
    <item>
      <title>Count γH2AX or 53BP1 foci per nucleus in ImageJ (Find Maxima, step by step)</title>
      <link>https://www.labcanvas.com/blog/count-foci-per-nucleus</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/count-foci-per-nucleus</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Count γH2AX or 53BP1 foci per nucleus in ImageJ: nuclei as ROIs, Find Maxima with the right prominence, counts per nucleus and % of cells with ≥5 foci.</description>
      <category>count foci ImageJ</category>
      <category>gamma H2AX foci quantification</category>
      <category>DNA damage foci counting</category>
      <category>53BP1 foci</category>
      <category>Find Maxima</category>
      <category>prominence</category>
      <category>foci per nucleus</category>
      <category>ROI Manager</category>
      <category>Fiji</category>
      <category>puncta counting</category>
    </item>
    <item>
      <title>How to measure d-spacing from HRTEM lattice fringes in ImageJ (profile and FFT)</title>
      <link>https://www.labcanvas.com/blog/d-spacing-hrtem-lattice-fringes</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/d-spacing-hrtem-lattice-fringes</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Measure d-spacing in ImageJ: a wide line across 10 fringes and Plot Profile (d = L ÷ N), or FFT spots read with Measure. Worked on Au (111), 0.235 nm.</description>
      <category>d spacing imagej</category>
      <category>lattice fringe measurement</category>
      <category>d spacing hrtem</category>
      <category>interplanar spacing tem</category>
      <category>fft imagej</category>
      <category>HRTEM</category>
      <category>lattice spacing</category>
      <category>power spectrum</category>
      <category>Plot Profile</category>
      <category>gold nanoparticles</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>IHC DAB quantification in ImageJ with colour deconvolution</title>
      <link>https://www.labcanvas.com/blog/dab-ihc-quantification</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/dab-ihc-quantification</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Quantify DAB IHC in ImageJ/Fiji: colour deconvolution with H-DAB vectors, % positive area, optical density, and why DAB intensity is not linear.</description>
      <category>color deconvolution ImageJ</category>
      <category>IHC quantification ImageJ</category>
      <category>DAB quantification</category>
      <category>ImageJ immunohistochemistry</category>
      <category>colour deconvolution</category>
      <category>H-DAB</category>
      <category>optical density</category>
      <category>percent positive area</category>
      <category>Fiji</category>
      <category>Color Threshold</category>
    </item>
    <item>
      <title>Feret diameter, circularity, aspect ratio and solidity in ImageJ, explained</title>
      <link>https://www.labcanvas.com/blog/feret-diameter-circularity</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/feret-diameter-circularity</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>What ImageJ shape descriptors mean: Feret and MinFeret, circularity, AR, roundness and solidity, with formulas, drawn shapes and real TEM and SEM numbers.</description>
      <category>feret diameter ImageJ</category>
      <category>circularity ImageJ</category>
      <category>solidity ImageJ</category>
      <category>shape descriptors ImageJ</category>
      <category>aspect ratio</category>
      <category>roundness</category>
      <category>MinFeret</category>
      <category>convex hull</category>
      <category>nanoparticle shape</category>
      <category>nanorod aspect ratio</category>
      <category>particle shape analysis</category>
    </item>
    <item>
      <title>Deep-learning cell segmentation in Fiji: StarDist, Cellpose and Weka (step by step)</title>
      <link>https://www.labcanvas.com/blog/fiji-stardist-cellpose-segmentation</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/fiji-stardist-cellpose-segmentation</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>When a threshold fails, segment cells in Fiji with StarDist, Cellpose or Trainable Weka: install, settings, then label image to ROIs and measurements.</description>
      <category>StarDist ImageJ</category>
      <category>Cellpose ImageJ</category>
      <category>ImageJ deep learning</category>
      <category>Trainable Weka Segmentation</category>
      <category>deepImageJ</category>
      <category>ImageJ segmentation plugin</category>
      <category>Fiji</category>
      <category>label image</category>
      <category>nuclei segmentation</category>
      <category>touching cells</category>
      <category>ROI Manager</category>
    </item>
    <item>
      <title>Stitch microscope tiles in Fiji (Grid/Collection stitching, step by step)</title>
      <link>https://www.labcanvas.com/blog/fiji-stitching-tiles</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/fiji-stitching-tiles</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Stitch overlapping microscope tiles in Fiji with Grid/Collection stitching: grid type, overlap, file names, fusion, and why an ImageJ montage is wrong.</description>
      <category>ImageJ stitching</category>
      <category>stitch images ImageJ</category>
      <category>image stitching ImageJ</category>
      <category>Fiji Grid/Collection stitching</category>
      <category>tile scan</category>
      <category>mosaic</category>
      <category>tile overlap</category>
      <category>TileConfiguration</category>
      <category>Make Montage</category>
      <category>phase correlation</category>
    </item>
    <item>
      <title>Fiji vs ImageJ: what&apos;s the difference, and which should you download?</title>
      <link>https://www.labcanvas.com/blog/fiji-vs-imagej</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/fiji-vs-imagej</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Fiji is ImageJ with plugins, Bio-Formats, an updater and scripting built in; ImageJ2 is the rewrite underneath. A comparison table and which to download.</description>
      <category>imagej vs fiji</category>
      <category>fiji vs imagej</category>
      <category>fiji is just imagej</category>
      <category>imagej2</category>
      <category>what is fiji imagej</category>
      <category>what is imagej called now</category>
      <category>ImageJ download</category>
      <category>Fiji download</category>
      <category>Bio-Formats</category>
      <category>ImageJ.JS</category>
    </item>
    <item>
      <title>FRAP analysis in ImageJ: mobile fraction and half-time, step by step</title>
      <link>https://www.labcanvas.com/blog/frap-analysis-mobile-fraction</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/frap-analysis-mobile-fraction</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>FRAP in ImageJ: bleach, reference and background ROIs, Multi Measure, double normalisation, an exponential recovery fit, then the mobile fraction and t½.</description>
      <category>frap analysis imagej</category>
      <category>frap mobile fraction calculation</category>
      <category>frap half time</category>
      <category>double normalization frap</category>
      <category>FRAP</category>
      <category>fluorescence recovery after photobleaching</category>
      <category>ROI Manager</category>
      <category>Multi Measure</category>
      <category>Curve Fitting</category>
      <category>exponential recovery</category>
      <category>immobile fraction</category>
    </item>
    <item>
      <title>Free western blot quantification software (now that Image Studio Lite is gone)</title>
      <link>https://www.labcanvas.com/blog/free-western-blot-quantification-software</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/free-western-blot-quantification-software</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Image Studio Lite is discontinued. Quantify western blots free in ImageJ (Analyze › Gels), step by step, with Image Lab and IOCBIO Gel compared.</description>
      <category>Image Studio Lite alternative</category>
      <category>free western blot analysis software</category>
      <category>western blot densitometry software free</category>
      <category>western blot quantification</category>
      <category>ImageJ gel analysis</category>
      <category>Image Lab</category>
      <category>IOCBIO Gel</category>
      <category>Empiria Studio</category>
      <category>densitometry</category>
      <category>fold change</category>
    </item>
    <item>
      <title>How to cite ImageJ and Fiji (with a methods sentence to copy)</title>
      <link>https://www.labcanvas.com/blog/how-to-cite-imagej</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/how-to-cite-imagej</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Cite ImageJ (Schneider et al. 2012), Fiji (Schindelin et al. 2012) or ImageJ2 (Rueden et al. 2017): DOIs, APA, Vancouver, BibTeX and methods sentences.</description>
      <category>ImageJ citation</category>
      <category>ImageJ software citation</category>
      <category>how to cite ImageJ</category>
      <category>ImageJ reference</category>
      <category>how to cite ImageJ in methods</category>
      <category>cite Fiji</category>
      <category>ImageJ2</category>
      <category>methods section</category>
      <category>BibTeX</category>
      <category>image analysis</category>
    </item>
    <item>
      <title>3D projection and 3D viewing in ImageJ (Image › Stacks › 3D Project)</title>
      <link>https://www.labcanvas.com/blog/imagej-3d-projection</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-3d-projection</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Make a rotating 3D view of a Z-stack with Image › Stacks › 3D Project in ImageJ, set the slice spacing, use Orthogonal Views, or Fiji&apos;s 3D Viewer.</description>
      <category>3d viewer imagej</category>
      <category>imagej 3d viewer</category>
      <category>3d reconstruction imagej</category>
      <category>imagej 3d reconstruction</category>
      <category>3D Project</category>
      <category>Z-stack</category>
      <category>voxel depth</category>
      <category>Orthogonal Views</category>
      <category>Fiji 3D Viewer</category>
      <category>volume rendering</category>
    </item>
    <item>
      <title>Crop, rotate, resize and convert images in ImageJ (without changing your data by accident)</title>
      <link>https://www.labcanvas.com/blog/imagej-basic-image-editing</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-basic-image-editing</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>How to crop, rotate, resize, zoom and convert to 8-bit or grayscale in ImageJ, and what each command does to pixel values and the scale, measured.</description>
      <category>how to crop in imagej</category>
      <category>how to rotate image in imagej</category>
      <category>imagej resize image</category>
      <category>imagej convert to grayscale</category>
      <category>how to merge images in imagej</category>
      <category>how to zoom in on imagej</category>
      <category>Image Crop</category>
      <category>Image Scale</category>
      <category>8-bit conversion</category>
      <category>pixel size</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>Deconvolution in ImageJ and Fiji: what it does and how to run it</title>
      <link>https://www.labcanvas.com/blog/imagej-deconvolution</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-deconvolution</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>What deconvolution does (the PSF, Richardson–Lucy), why FD Math Deconvolve fails on real images, and how to run Richardson–Lucy in ImageJ and Fiji.</description>
      <category>deconvolution ImageJ</category>
      <category>ImageJ deconvolution</category>
      <category>deconvolution in ImageJ</category>
      <category>Richardson-Lucy</category>
      <category>point spread function</category>
      <category>PSF</category>
      <category>FD Math</category>
      <category>DeconvolutionLab2</category>
      <category>Iterative Deconvolve 3D</category>
      <category>Fiji</category>
      <category>fluorescence microscopy</category>
    </item>
    <item>
      <title>FFT bandpass filter and edge detection in ImageJ (with before/after examples)</title>
      <link>https://www.labcanvas.com/blog/imagej-fft-bandpass-edge-detection</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-fft-bandpass-edge-detection</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>FFT in ImageJ step by step: Process › FFT, Bandpass Filter settings, stripe removal and Find Edges, with before/after pictures and when filtering is safe.</description>
      <category>fft imagej</category>
      <category>imagej fft</category>
      <category>edge detection imagej</category>
      <category>imagej edge detection</category>
      <category>FFT bandpass filter</category>
      <category>Find Edges</category>
      <category>Sobel</category>
      <category>power spectrum</category>
      <category>remove stripes</category>
      <category>uneven background</category>
      <category>segmentation</category>
    </item>
    <item>
      <title>Check for saturated pixels in ImageJ: histogram, HiLo LUT and the numbers</title>
      <link>https://www.labcanvas.com/blog/imagej-histogram-saturation</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-histogram-saturation</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Check saturation in ImageJ with Analyze › Histogram, the HiLo LUT and Min/Max, on a clipped example with its spike at 65535 and what it does to data.</description>
      <category>ImageJ histogram</category>
      <category>histogram ImageJ</category>
      <category>saturated pixels</category>
      <category>check saturation</category>
      <category>HiLo LUT</category>
      <category>overexposed</category>
      <category>clipping</category>
      <category>Analyze Histogram</category>
      <category>min and max gray value</category>
      <category>fluorescence quantification</category>
      <category>image integrity</category>
    </item>
    <item>
      <title>LUTs in ImageJ: which lookup table to use (and colour-blind-safe choices)</title>
      <link>https://www.labcanvas.com/blog/imagej-lut</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-lut</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>ImageJ lookup tables compared on one image: Grays, Fire, viridis, HiLo and the rest, how to add a calibration bar, and colour-blind-safe channel colours.</description>
      <category>ImageJ LUT</category>
      <category>ImageJ LUTs</category>
      <category>lookup tables ImageJ</category>
      <category>LUT ImageJ</category>
      <category>calibration bar</category>
      <category>Fire LUT</category>
      <category>viridis</category>
      <category>HiLo</category>
      <category>colour blind</category>
      <category>green magenta</category>
      <category>false colour</category>
    </item>
    <item>
      <title>ImageJ and Fiji on a Mac: install, Apple Silicon and &quot;can&apos;t be opened&quot; fixes</title>
      <link>https://www.labcanvas.com/blog/imagej-mac</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-mac</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Download ImageJ or Fiji for Mac (Apple Silicon or Intel), fix &quot;can&apos;t be opened&quot; and &quot;damaged&quot; errors, set the memory, and the no-install option.</description>
      <category>download ImageJ for Mac</category>
      <category>ImageJ for Mac</category>
      <category>ImageJ Mac download</category>
      <category>Fiji download Mac</category>
      <category>ImageJ for Mac M1</category>
      <category>how to use ImageJ on Mac</category>
      <category>Apple Silicon</category>
      <category>Gatekeeper</category>
      <category>Fiji</category>
      <category>ImageJ memory</category>
    </item>
    <item>
      <title>ImageJ macros for beginners: record a macro and batch-process a folder</title>
      <link>https://www.labcanvas.com/blog/imagej-macros-batch-processing</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-macros-batch-processing</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Record an ImageJ macro with Plugins › Macros › Record, run it from the editor, then batch-process a folder with Process › Batch › Macro. Step by step.</description>
      <category>imagej macro</category>
      <category>imagej macros</category>
      <category>macro language imagej</category>
      <category>imagej macro recorder</category>
      <category>imagej batch processing</category>
      <category>batch processing imagej</category>
      <category>Process Batch Macro</category>
      <category>Analyze Particles</category>
      <category>Fiji macro</category>
      <category>automate ImageJ</category>
    </item>
    <item>
      <title>Make a movie from an image stack or time-lapse in ImageJ (AVI, GIF, MP4)</title>
      <link>https://www.labcanvas.com/blog/imagej-make-movie-from-stack</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-make-movie-from-stack</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Turn a folder of frames or a time-lapse stack into an AVI, GIF or MP4 in ImageJ: Image Sequence, a time stamp, a scale bar, frame rate, and saving.</description>
      <category>imagej make video from stack</category>
      <category>imagej save as mp4</category>
      <category>mp4 imagej</category>
      <category>imagej image sequence</category>
      <category>imagej avi</category>
      <category>animated gif imagej</category>
      <category>time stamp</category>
      <category>time-lapse movie</category>
      <category>frame rate</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>Plot Profile in ImageJ: line scans, wide lines and intensity profiles</title>
      <link>https://www.labcanvas.com/blog/imagej-plot-profile</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-plot-profile</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Plot Profile in ImageJ: draw a line, press Ctrl K, set the line width to average noise, copy the values, plot two channels and profile a rectangle.</description>
      <category>ImageJ plot profile</category>
      <category>plot profile ImageJ</category>
      <category>line scan ImageJ</category>
      <category>intensity profile</category>
      <category>line profile</category>
      <category>line width</category>
      <category>multichannel profile</category>
      <category>Fiji</category>
      <category>colocalisation line scan</category>
      <category>lattice fringes</category>
    </item>
    <item>
      <title>ROI Manager in ImageJ: measure many regions, save them and open them anywhere</title>
      <link>https://www.labcanvas.com/blog/imagej-roi-manager</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-roi-manager</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Open the ROI Manager in ImageJ (Analyze › Tools › ROI Manager), add ROIs with T, measure them on every channel, save RoiSet.zip and reopen it later.</description>
      <category>ROI Manager ImageJ</category>
      <category>ImageJ ROI</category>
      <category>how to open ROI Manager</category>
      <category>ImageJ save ROI</category>
      <category>select multiple ROI</category>
      <category>RoiSet.zip</category>
      <category>Multi Measure</category>
      <category>measure two channels</category>
      <category>Fiji</category>
      <category>regions of interest</category>
    </item>
    <item>
      <title>ImageJ threshold methods compared, with pictures</title>
      <link>https://www.labcanvas.com/blog/imagej-threshold-methods</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-threshold-methods</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>All 16 ImageJ auto threshold methods on one image, with the threshold and % area each gives, which method suits which image, and how to apply it.</description>
      <category>threshold ImageJ</category>
      <category>ImageJ thresholding</category>
      <category>ImageJ auto threshold methods</category>
      <category>which threshold method</category>
      <category>Otsu vs Triangle</category>
      <category>segmentation ImageJ</category>
      <category>setAutoThreshold</category>
      <category>Convert to Mask</category>
      <category>dark background</category>
      <category>Fiji Auto Threshold</category>
      <category>image segmentation</category>
    </item>
    <item>
      <title>Install ImageJ or Fiji on Windows 10 and 11</title>
      <link>https://www.labcanvas.com/blog/imagej-windows</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/imagej-windows</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Download and install Fiji or ImageJ on Windows 10 and 11: the right zip, where to unzip it (not Program Files), Java, memory, and where files go.</description>
      <category>ImageJ download Windows</category>
      <category>Fiji download Windows</category>
      <category>ImageJ for Windows</category>
      <category>install Fiji Windows 11</category>
      <category>ImageJ Windows 10</category>
      <category>ImageJ memory</category>
      <category>Program Files</category>
      <category>Fiji</category>
      <category>Java</category>
    </item>
    <item>
      <title>How to make a kymograph in ImageJ and measure velocities</title>
      <link>https://www.labcanvas.com/blog/kymograph-imagej</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/kymograph-imagej</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Make a kymograph in ImageJ: a line along the track, Image › Stacks › Reslice, then a line on each streak gives velocity = Δx ÷ Δt, with a worked example.</description>
      <category>ImageJ kymograph</category>
      <category>kymograph ImageJ</category>
      <category>how to make a kymograph</category>
      <category>velocity from kymograph</category>
      <category>Reslice</category>
      <category>KymoResliceWide</category>
      <category>KymographBuilder</category>
      <category>axonal transport</category>
      <category>time-lapse</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>Z Project in ImageJ: maximum, average and sum projections compared</title>
      <link>https://www.labcanvas.com/blog/maximum-intensity-projection</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/maximum-intensity-projection</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Image › Stacks › Z Project in ImageJ: what Max Intensity, Average, Sum Slices, SD, Min and Median give, when Sum beats Max, and how to check depth.</description>
      <category>Z project ImageJ</category>
      <category>maximum intensity projection</category>
      <category>ImageJ Z projection</category>
      <category>stack projection</category>
      <category>sum slices</category>
      <category>average intensity projection</category>
      <category>orthogonal views</category>
      <category>Z-stack</category>
      <category>confocal</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>How to measure fluorescence intensity in ImageJ (Mean, IntDen, RawIntDen and CTCF)</title>
      <link>https://www.labcanvas.com/blog/measure-fluorescence-intensity-imagej</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/measure-fluorescence-intensity-imagej</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Measure fluorescence in ImageJ: Mean, IntDen and RawIntDen explained, CTCF = IntDen − Area × background worked through, and the 8-bit and saturation traps.</description>
      <category>integrated density ImageJ</category>
      <category>how to measure fluorescence intensity in ImageJ</category>
      <category>what is integrated density</category>
      <category>mean gray value</category>
      <category>CTCF</category>
      <category>corrected total cell fluorescence</category>
      <category>RawIntDen</category>
      <category>quantify fluorescence intensity ImageJ</category>
      <category>background subtraction</category>
      <category>Set Measurements</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>Merge, split and overlay channels in ImageJ (and make a composite figure)</title>
      <link>https://www.labcanvas.com/blog/merge-channels-imagej</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/merge-channels-imagej</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Merge channels in ImageJ with Image › Color › Merge Channels, split them with Split Channels, overlay with Add Image, and build a colour-blind-safe figure.</description>
      <category>ImageJ merge channels</category>
      <category>overlay ImageJ</category>
      <category>how to split channels in ImageJ</category>
      <category>how to merge images in ImageJ</category>
      <category>composite image</category>
      <category>Channels Tool</category>
      <category>Stack to RGB</category>
      <category>green magenta</category>
      <category>colour-blind safe</category>
      <category>fluorescence figure</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>Image integrity: what you may and may not do to microscopy and blot images</title>
      <link>https://www.labcanvas.com/blog/microscopy-image-integrity</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/microscopy-image-integrity</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>What journals allow when you adjust microscopy and blot images: linear whole-image changes, gamma disclosed, no cloning or selective edits, in ImageJ.</description>
      <category>image manipulation guidelines microscopy</category>
      <category>western blot image integrity</category>
      <category>journal image guidelines</category>
      <category>image integrity</category>
      <category>brightness and contrast</category>
      <category>gamma adjustment</category>
      <category>research integrity</category>
      <category>blot splicing</category>
      <category>ImageJ</category>
      <category>figure preparation</category>
    </item>
    <item>
      <title>Nanoparticle size distribution from TEM images in ImageJ (step by step)</title>
      <link>https://www.labcanvas.com/blog/nanoparticle-size-distribution-tem</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/nanoparticle-size-distribution-tem</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Nanoparticle size from TEM in ImageJ: scale, threshold, watershed, Analyze Particles with Feret, then the size histogram and mean ± SD, worked through.</description>
      <category>nanoparticle size distribution ImageJ</category>
      <category>TEM particle size analysis</category>
      <category>how to measure particle size in ImageJ</category>
      <category>particle size histogram TEM</category>
      <category>Feret diameter</category>
      <category>equivalent diameter</category>
      <category>gold nanoparticles</category>
      <category>watershed</category>
      <category>analyze particles</category>
      <category>TEM image analysis</category>
    </item>
    <item>
      <title>Nanorod and nanowire length, width and aspect ratio from SEM images in ImageJ</title>
      <link>https://www.labcanvas.com/blog/nanowire-length-aspect-ratio-sem</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/nanowire-length-aspect-ratio-sem</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Measure nanorod and nanowire length, width and aspect ratio from SEM images in ImageJ: Feret, MinFeret, fit ellipse, edge rods, and why not to watershed.</description>
      <category>nanowire length ImageJ</category>
      <category>nanorod aspect ratio</category>
      <category>measure nanowire diameter SEM</category>
      <category>Feret diameter</category>
      <category>MinFeret</category>
      <category>aspect ratio ImageJ</category>
      <category>SEM image analysis</category>
      <category>Analyze Particles</category>
      <category>nanorod size distribution</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>Neurite length and branching in ImageJ: Skeletonize and Analyze Skeleton</title>
      <link>https://www.labcanvas.com/blog/neurite-length-skeleton-analysis</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/neurite-length-skeleton-analysis</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Neurite length and branching in ImageJ: threshold, Process › Binary › Skeletonize, then Analyze Skeleton (Fiji) or a macro. Why diagonal steps matter.</description>
      <category>skeletonize imagej</category>
      <category>imagej skeletonize</category>
      <category>analyze skeleton</category>
      <category>neurite length imagej</category>
      <category>branch length</category>
      <category>neurite outgrowth</category>
      <category>skeleton analysis</category>
      <category>branch points</category>
      <category>Fiji</category>
      <category>AnalyzeSkeleton</category>
    </item>
    <item>
      <title>Nuclear/cytoplasmic ratio in ImageJ: quantify NF-κB, YAP or TFEB translocation</title>
      <link>https://www.labcanvas.com/blog/nuclear-cytoplasmic-ratio</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/nuclear-cytoplasmic-ratio</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Measure the nuclear/cytoplasmic ratio in ImageJ step by step: nuclei from DAPI, a cytoplasm ring with Enlarge and Make Band, and an N/C table per cell.</description>
      <category>nuclear cytoplasmic ratio ImageJ</category>
      <category>NF-kB translocation quantification</category>
      <category>YAP nuclear localization quantification</category>
      <category>TFEB nuclear translocation</category>
      <category>N/C ratio</category>
      <category>Make Band</category>
      <category>Enlarge selection</category>
      <category>ROI Manager</category>
      <category>cytoplasmic ring</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>How to open .czi, .nd2, .lif and other microscope files in ImageJ (Bio-Formats)</title>
      <link>https://www.labcanvas.com/blog/open-czi-nd2-files-imagej</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/open-czi-nd2-files-imagej</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Open Zeiss .czi, Nikon .nd2 and Leica .lif files in ImageJ with Bio-Formats (built into Fiji), keep the pixel size, and fix &quot;Unsupported format&quot;.</description>
      <category>Bio-Formats ImageJ</category>
      <category>how to open czi files in ImageJ</category>
      <category>how to open nd2 files in ImageJ</category>
      <category>ImageJ Bio-Formats plugin</category>
      <category>lif files ImageJ</category>
      <category>OME-TIFF</category>
      <category>Fiji</category>
      <category>pixel size</category>
      <category>microscope file formats</category>
      <category>Unsupported format or file not found</category>
    </item>
    <item>
      <title>Open DICOM files in ImageJ (and a series as a stack)</title>
      <link>https://www.labcanvas.com/blog/open-dicom-imagej</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Open DICOM files in ImageJ with File › Open, a whole series as a stack with Import › Image Sequence, read the tags, measure HU, and open compressed DICOM.</description>
      <category>ImageJ DICOM</category>
      <category>compressed DICOM ImageJ</category>
      <category>is ImageJ good for medical imaging</category>
      <category>open DICOM series</category>
      <category>DICOM stack</category>
      <category>Hounsfield units</category>
      <category>Show Info</category>
      <category>Bio-Formats</category>
      <category>CT</category>
      <category>Fiji</category>
    </item>
    <item>
      <title>Particle tracking in ImageJ (TrackMate) and MSD: a practical guide</title>
      <link>https://www.labcanvas.com/blog/particle-tracking-msd</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/particle-tracking-msd</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Track particles in ImageJ with TrackMate (Fiji) or Find Maxima, then get the diffusion coefficient from the MSD: MSD = 4Dt in 2D, with a worked example.</description>
      <category>particle tracker ImageJ</category>
      <category>particle tracking ImageJ</category>
      <category>TrackMate ImageJ</category>
      <category>MSD analysis</category>
      <category>mean squared displacement</category>
      <category>diffusion coefficient from tracking</category>
      <category>single-particle tracking</category>
      <category>Find Maxima</category>
      <category>Fiji</category>
      <category>drift correction</category>
    </item>
    <item>
      <title>Porosity and pore size from SEM images in ImageJ (AAO, membranes, coatings)</title>
      <link>https://www.labcanvas.com/blog/porosity-pore-size-sem-image</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/porosity-pore-size-sem-image</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Porosity and pore size from an SEM image in ImageJ: threshold the pores, read %Area as porosity, then Analyze Particles for pore areas and diameters.</description>
      <category>ImageJ porosity</category>
      <category>porosity from SEM image</category>
      <category>pore size distribution SEM ImageJ</category>
      <category>measure pore size SEM</category>
      <category>area fraction ImageJ</category>
      <category>anodic aluminium oxide</category>
      <category>AAO membrane</category>
      <category>porous coating</category>
      <category>equivalent diameter</category>
      <category>analyze particles</category>
      <category>SEM image analysis</category>
    </item>
    <item>
      <title>Use ImageJ from Python with PyImageJ (a gentle start)</title>
      <link>https://www.labcanvas.com/blog/pyimagej-python</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Install PyImageJ, start ImageJ from Python with imagej.init, run your ImageJ macro, and get the image as NumPy and the Results table as pandas.</description>
      <category>PyImageJ</category>
      <category>ImageJ Python</category>
      <category>imagej.init</category>
      <category>run ImageJ macro from Python</category>
      <category>ImageJ NumPy</category>
      <category>ImageJ pandas</category>
      <category>Fiji Python</category>
      <category>ImageJ2</category>
      <category>batch processing</category>
      <category>Jupyter</category>
    </item>
    <item>
      <title>Rolling-ball background subtraction in ImageJ: how to choose the radius</title>
      <link>https://www.labcanvas.com/blog/rolling-ball-background-subtraction</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/rolling-ball-background-subtraction</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Subtract background in ImageJ: Process › Subtract Background, a rolling ball radius at least the largest object&apos;s, Light background off for fluorescence.</description>
      <category>subtract background ImageJ</category>
      <category>ImageJ subtract background</category>
      <category>background subtraction ImageJ</category>
      <category>rolling ball radius</category>
      <category>rolling ball algorithm</category>
      <category>sliding paraboloid</category>
      <category>uneven illumination</category>
      <category>Fiji</category>
      <category>fluorescence microscopy</category>
      <category>line profile</category>
    </item>
    <item>
      <title>Wound healing (scratch) assay analysis in ImageJ: % closure step by step</title>
      <link>https://www.labcanvas.com/blog/scratch-wound-healing-assay-analysis</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/scratch-wound-healing-assay-analysis</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Measure a scratch wound in ImageJ: variance filter, threshold and Analyze Particles per frame, then % closure and closure rate, with a worked example.</description>
      <category>wound healing assay imagej</category>
      <category>scratch assay analysis</category>
      <category>wound closure percentage calculation</category>
      <category>wound healing size tool imagej</category>
      <category>scratch assay</category>
      <category>migration assay</category>
      <category>variance filter</category>
      <category>closure rate</category>
      <category>time-lapse</category>
      <category>ImageJ</category>
    </item>
    <item>
      <title>Sholl analysis in ImageJ/Fiji and online (step by step)</title>
      <link>https://www.labcanvas.com/blog/sholl-analysis</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Sholl analysis step by step: circles around the cell body, crossings per radius, the Sholl plot, critical radius and ramification index, in Fiji (SNT) or with an ImageJ macro.</description>
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      <category>sholl analysis online</category>
      <category>sholl analysis fiji</category>
      <category>dendritic complexity</category>
      <category>dendritic arborization</category>
      <category>ramification index</category>
      <category>critical radius</category>
      <category>neuron morphology</category>
      <category>SNT</category>
      <category>Sholl plot</category>
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    <item>
      <title>Tube formation assay quantification in ImageJ (and the Angiogenesis Analyzer)</title>
      <link>https://www.labcanvas.com/blog/tube-formation-assay-quantification</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/tube-formation-assay-quantification</guid>
      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Quantify a tube formation assay in ImageJ step by step: total tube length, junctions, segments and meshes, plus the Angiogenesis Analyzer and AngioTool.</description>
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      <category>Angiogenesis Analyzer ImageJ</category>
      <category>AngioTool</category>
      <category>endothelial tube formation analysis</category>
      <category>HUVEC tube formation</category>
      <category>skeletonize</category>
      <category>junctions and meshes</category>
      <category>total tube length</category>
      <category>angiogenesis assay</category>
      <category>Fiji</category>
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    <item>
      <title>Watershed in ImageJ: separate touching particles (and when not to)</title>
      <link>https://www.labcanvas.com/blog/watershed-touching-particles</link>
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      <pubDate>Fri, 06 Nov 2026 09:00:00 GMT</pubDate>
      <description>Split touching nuclei and nanoparticles with Process › Binary › Watershed in ImageJ, with before and after counts, and why it cuts nanorods to pieces.</description>
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      <category>watershed ImageJ</category>
      <category>separate touching particles</category>
      <category>split nuclei</category>
      <category>touching cells</category>
      <category>distance map</category>
      <category>ultimate points</category>
      <category>binary watershed</category>
      <category>over-segmentation</category>
      <category>Analyze Particles</category>
      <category>nanoparticle counting</category>
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    <item>
      <title>Crystal structure and 2D-material figures: VESTA, Mercury, CrystalMaker, Avogadro, OVITO and LabCanvas compared</title>
      <link>https://www.labcanvas.com/blog/crystal-structure-visualization-software</link>
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      <pubDate>Mon, 26 Oct 2026 09:00:00 GMT</pubDate>
      <description>Which tool for crystal structure and 2D-material figures? VESTA, CrystalMaker, Mercury, Avogadro, Jmol, OVITO, the Materials Project viewer and LabCanvas compared: licence, platforms, file formats, rendering and how to cite each.</description>
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      <category>VESTA</category>
      <category>CIF</category>
      <category>2D materials</category>
      <category>materials science figures</category>
      <category>comparison</category>
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    <item>
      <title>Free tools for scientific figures in 2026: BioRender, Inkscape, Affinity, Canva, PowerPoint and more</title>
      <link>https://www.labcanvas.com/blog/free-tools-scientific-figures</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/free-tools-scientific-figures</guid>
      <pubDate>Mon, 26 Oct 2026 09:00:00 GMT</pubDate>
      <description>An honest comparison of tools for scientific figures: BioRender, Mind the Graph, Inkscape, Affinity, Canva, PowerPoint, Adobe Illustrator and LabCanvas. What each free plan includes, publication rights, file formats and who each one suits.</description>
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      <category>free tools</category>
      <category>BioRender alternative</category>
      <category>Inkscape</category>
      <category>comparison</category>
      <category>graphical abstract</category>
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    <item>
      <title>Journal figure size guide: column widths, DPI and fonts for 38 journals</title>
      <link>https://www.labcanvas.com/blog/journal-figure-size-guide</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/journal-figure-size-guide</guid>
      <pubDate>Mon, 26 Oct 2026 09:00:00 GMT</pubDate>
      <description>Figure requirements for 38 journals in one table: single, 1.5 and double column widths in mm, maximum height, DPI for photos and line art, fonts and file types, each linked to the journal’s author guidelines.</description>
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      <category>DPI</category>
      <category>column width</category>
      <category>author guidelines</category>
      <category>scientific figures</category>
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    <item>
      <title>A free GraphPad Prism alternative: graphs and statistics in your browser</title>
      <link>https://www.labcanvas.com/blog/graphpad-prism-alternative</link>
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      <pubDate>Mon, 26 Oct 2026 09:00:00 GMT</pubDate>
      <description>Looking for a free GraphPad Prism alternative? What LabCanvas Graphs does (data tables, t tests, ANOVA, curve fits, survival, cluster analysis, 70 graph types checked against SciPy), what it does not, and when Prism is still the better choice.</description>
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      <category>statistics</category>
      <category>scientific graphs</category>
      <category>ANOVA</category>
      <category>dose-response curve</category>
      <category>comparison</category>
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      <title>The LabCanvas Figure editor: vector scientific illustration in your browser</title>
      <link>https://www.labcanvas.com/blog/figure-editor-scientific-illustration</link>
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      <pubDate>Sun, 18 Oct 2026 09:00:00 GMT</pubDate>
      <description>How to make journal figures and graphical abstracts in the LabCanvas Figure editor: vector tools, 700+ adjustable science objects, lab glassware that connects, LaTeX equations, and export at the width and DPI your journal asks for.</description>
      <category>figure editor</category>
      <category>scientific illustration</category>
      <category>graphical abstract</category>
      <category>journal figures</category>
      <category>vector graphics</category>
      <category>BioRender alternative</category>
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      <title>LabCanvas Slides: scientific presentations built from editable figures</title>
      <link>https://www.labcanvas.com/blog/slides-scientific-presentations</link>
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      <pubDate>Sun, 18 Oct 2026 09:00:00 GMT</pubDate>
      <description>How to build lab meetings, conference talks and lectures in LabCanvas Slides: a slide strip, layouts and themes, transitions and motion paths, speaker notes, full-screen presenting and a vector PDF of the deck.</description>
      <category>scientific presentation</category>
      <category>slides</category>
      <category>conference talk</category>
      <category>lab meeting</category>
      <category>PowerPoint alternative</category>
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    <item>
      <title>LabCanvas Research Poster: conference posters that arrange themselves</title>
      <link>https://www.labcanvas.com/blog/research-poster-maker</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/research-poster-maker</guid>
      <pubDate>Sun, 18 Oct 2026 09:00:00 GMT</pubDate>
      <description>How to make an A0, A1 or 48 × 36 in research poster in LabCanvas Research Poster: blocks that stack in columns and re-flow their text, themes and block styles, QR codes, and a print-ready vector PDF.</description>
      <category>research poster</category>
      <category>conference poster</category>
      <category>academic poster</category>
      <category>A0 poster</category>
      <category>poster template</category>
      <category>betterposter</category>
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    <item>
      <title>MolDraw online: free chemical structure drawing in your browser</title>
      <link>https://www.labcanvas.com/blog/moldraw-chemical-structure-drawing</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/moldraw-chemical-structure-drawing</guid>
      <pubDate>Sun, 18 Oct 2026 09:00:00 GMT</pubDate>
      <description>Draw molecules and reaction schemes online, free, with nothing to install. LabCanvas MolDraw: atoms, bonds, rings and charges, reaction arrows, structures from PubChem, SMILES, a 3D view of the same molecule, and placing structures in figures.</description>
      <category>chemical structure drawing</category>
      <category>molecule editor</category>
      <category>reaction scheme</category>
      <category>ChemDraw alternative</category>
      <category>SMILES</category>
      <category>chemistry</category>
    </item>
    <item>
      <title>The LabCanvas 3D Studio: adjustable 3D models of cells, nanomaterials and devices</title>
      <link>https://www.labcanvas.com/blog/3d-studio-scientific-3d-models</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/3d-studio-scientific-3d-models</guid>
      <pubDate>Sun, 18 Oct 2026 09:00:00 GMT</pubDate>
      <description>How to make 3D scientific renders in the LabCanvas 3D Studio: adjustable models of cells, viruses, nanoparticles, 2D materials, MOFs and devices, molecules from PubChem, proteins from the PDB, crystals from CIF files, and renders placed in figures.</description>
      <category>3D scientific illustration</category>
      <category>nanomaterials 3D</category>
      <category>cell 3D model</category>
      <category>crystal structure</category>
      <category>MOF</category>
      <category>ray tracing</category>
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    <item>
      <title>The LabCanvas Protein viewer: PDB structures styled for figures</title>
      <link>https://www.labcanvas.com/blog/protein-viewer-pdb-structures</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/protein-viewer-pdb-structures</guid>
      <pubDate>Sun, 18 Oct 2026 09:00:00 GMT</pubDate>
      <description>How to show a protein structure in the LabCanvas Protein viewer: load any PDB ID or your own PDB and mmCIF file, choose cartoon, surface or ball-and-stick, colour by chain or secondary structure, select residues on the sequence and snapshot a transparent PNG for your figure.</description>
      <category>protein structure</category>
      <category>PDB viewer</category>
      <category>molecular visualization</category>
      <category>structural biology</category>
      <category>AlphaFold</category>
      <category>PyMOL alternative</category>
    </item>
    <item>
      <title>LabCanvas Graphs &amp; statistics: 70 scientific graph types with checked statistics</title>
      <link>https://www.labcanvas.com/blog/graphs-statistics-scientific-plots</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/graphs-statistics-scientific-plots</guid>
      <pubDate>Sun, 18 Oct 2026 09:00:00 GMT</pubDate>
      <description>A visual guide to LabCanvas Graphs &amp; statistics: Prism-style data tables, 70 graph types from scatter dot plots to Kaplan–Meier, volcano and PAE plots, t tests, ANOVA, curve fits and survival tests checked against SciPy, and graphs that stay linked to their figure.</description>
      <category>scientific graphs</category>
      <category>statistics</category>
      <category>GraphPad Prism alternative</category>
      <category>ANOVA</category>
      <category>Kaplan-Meier</category>
      <category>volcano plot</category>
      <category>dose-response curve</category>
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    <item>
      <title>LabCanvas Optics: draw optical setups with the beam path simulated live</title>
      <link>https://www.labcanvas.com/blog/optics-optical-setup-simulator</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/optics-optical-setup-simulator</guid>
      <pubDate>Sun, 18 Oct 2026 09:00:00 GMT</pubDate>
      <description>How to build optical setup diagrams in LabCanvas Optics: lasers, lenses, mirrors, beam splitters, gratings and detectors on a breadboard, rays and beams traced as you move parts, interference, ready-made setups and clean schematics for figures.</description>
      <category>optical setup diagram</category>
      <category>ray tracing</category>
      <category>optics simulation</category>
      <category>laser setup</category>
      <category>interferometer</category>
      <category>physics illustration</category>
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    <item>
      <title>The LabCanvas Pixel editor: edit micrographs and photos inside your figure</title>
      <link>https://www.labcanvas.com/blog/pixel-editor-microscopy-images</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/pixel-editor-microscopy-images</guid>
      <pubDate>Sun, 18 Oct 2026 09:00:00 GMT</pubDate>
      <description>How to adjust microscopy images and photos in the LabCanvas Pixel editor: crop, levels, curves and exposure, false-colour lookup tables, healing and clone stamp, selections and masks, with an edit log for your methods section.</description>
      <category>microscopy image editing</category>
      <category>image processing</category>
      <category>figure preparation</category>
      <category>lookup tables</category>
      <category>image integrity</category>
      <category>Photoshop alternative</category>
    </item>
    <item>
      <title>What is LabCanvas? One workspace for scientific illustration, data and presentation</title>
      <link>https://www.labcanvas.com/blog/what-is-labcanvas</link>
      <guid isPermaLink="true">https://www.labcanvas.com/blog/what-is-labcanvas</guid>
      <pubDate>Wed, 14 Oct 2026 09:00:00 GMT</pubDate>
      <description>A guide to LabCanvas: ten connected apps for figures, molecules, 3D crystals, graphs, slides and posters, the workflows between them, ready-made templates, and why one editable canvas makes scientific illustration faster to learn and easier to change.</description>
      <category>LabCanvas</category>
      <category>scientific illustration</category>
      <category>graphical abstracts</category>
      <category>workflows</category>
      <category>chemistry</category>
      <category>materials science</category>
    </item>
    <item>
      <title>A BioRender alternative for scientific figures: what LabCanvas does differently</title>
      <link>https://www.labcanvas.com/blog/biorender-alternative</link>
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      <pubDate>Thu, 08 Oct 2026 09:00:00 GMT</pubDate>
      <description>Looking for a BioRender alternative? An honest comparison with LabCanvas: adjustable objects, vector tools, 3D and graphs, and when BioRender fits better.</description>
      <category>BioRender alternative</category>
      <category>scientific illustration</category>
      <category>comparison</category>
      <category>graphical abstracts</category>
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