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basler cmos a2a1920 160umbas camera  (Basler)


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    Basler basler cmos a2a1920 160umbas camera
    Basler Cmos A2a1920 160umbas Camera, supplied by Basler, used in various techniques. Bioz Stars score: 95/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/basler cmos a2a1920 160umbas camera/product/Basler
    Average 95 stars, based on 22 article reviews
    basler cmos a2a1920 160umbas camera - by Bioz Stars, 2026-05
    95/100 stars

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    Experimental setup for imaging the hepatic microvasculature in vivo . a ) Rat preparation viewed from above. Images were acquired from a region (blue rectangle) of the left lateral lobe of the liver. b ) A bright-field image of the liver surface vasculature: terminal central venule (tCV), terminal portal venule (tPV), and sinusoids. c ) Laser speckle imaging setup. The liver surface was illuminated with a 785 nm laser diode; the scattered light was captured by a CMOS camera (see Methods). d ) Raw images were first stabilized by matching the position of the motion marker. The temporal laser speckle contrast and the temporal blood flow index (tBFI) were calculated from the stabilized images. tBFI was averaged over time to obtain tBFI maps. e ) A tBFI map showing hepatic microvessels. See Fig. S1 for a tBFI map obtained from a larger region of the liver. f,g ) Close-up of the terminal central venules (f) and sinusoids (g). See Fig. S2 showing sinusoids in another rat.

    Journal: Biomedical Optics Express

    Article Title: Laser speckle contrast imaging of hepatic microcirculation

    doi: 10.1364/BOE.554663

    Figure Lengend Snippet: Experimental setup for imaging the hepatic microvasculature in vivo . a ) Rat preparation viewed from above. Images were acquired from a region (blue rectangle) of the left lateral lobe of the liver. b ) A bright-field image of the liver surface vasculature: terminal central venule (tCV), terminal portal venule (tPV), and sinusoids. c ) Laser speckle imaging setup. The liver surface was illuminated with a 785 nm laser diode; the scattered light was captured by a CMOS camera (see Methods). d ) Raw images were first stabilized by matching the position of the motion marker. The temporal laser speckle contrast and the temporal blood flow index (tBFI) were calculated from the stabilized images. tBFI was averaged over time to obtain tBFI maps. e ) A tBFI map showing hepatic microvessels. See Fig. S1 for a tBFI map obtained from a larger region of the liver. f,g ) Close-up of the terminal central venules (f) and sinusoids (g). See Fig. S2 showing sinusoids in another rat.

    Article Snippet: The scattered light passed through a linear polarizing filter and was captured by a CMOS camera (Basler acA2048-90umNIR, 5.5 μ m pixel size, 8-bit mode).

    Techniques: Imaging, In Vivo, Marker