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label blood vessels  (Vector Laboratories)


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    Vector Laboratories label blood vessels
    Label Blood Vessels, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 284 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/label blood vessels/product/Vector Laboratories
    Average 96 stars, based on 284 article reviews
    label blood vessels - by Bioz Stars, 2026-03
    96/100 stars

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    Image Search Results


    Confocal images of retinal vessels. (a) Retinal arterioles (a), venules (v), and capillaries are filled with dextran fluorescein isothiocyanate and imaged with confocal microscopy. The optic disc is at the lower left. The luminal diameter of the upper arteriole is measured with confocal line scans (black line). The nearby white bar indicates the location of the flickering light stimulus. Scale bar, 250 μm. (b) Line scan image obtained from the arteriole in (a). Distance (across the black line in (a)) is plotted as a function of time. A flickering light (white bar in (b)) evokes vessel dilation, indicated by the widening of the vessel cross section. The uneven edges of the vessel are caused by a respiratory movement artifact. Modified from ref. (12).

    Journal: Methods in molecular biology (Clifton, N.J.)

    Article Title: Assessment of Glial Function in the In Vivo Retina

    doi: 10.1007/978-1-61779-452-0_33

    Figure Lengend Snippet: Confocal images of retinal vessels. (a) Retinal arterioles (a), venules (v), and capillaries are filled with dextran fluorescein isothiocyanate and imaged with confocal microscopy. The optic disc is at the lower left. The luminal diameter of the upper arteriole is measured with confocal line scans (black line). The nearby white bar indicates the location of the flickering light stimulus. Scale bar, 250 μm. (b) Line scan image obtained from the arteriole in (a). Distance (across the black line in (a)) is plotted as a function of time. A flickering light (white bar in (b)) evokes vessel dilation, indicated by the widening of the vessel cross section. The uneven edges of the vessel are caused by a respiratory movement artifact. Modified from ref. (12).

    Article Snippet: Blood Vessel Labeling Dextran fluorescein isothiocyanate, 2,000,000 MW (Sigma) dissolved in saline (3% solution).

    Techniques: Confocal Microscopy, Modification

    Glial cells of the retina. Glial cells (green) are labeled with the Ca2+ indicator dye Oregon Green 488 BAPTA-1 and vessels (orange) by intravenous ejection of dextran rhodamine B isothiocyanate in this confocal image of the retina. Several astrocytes (arrows) are visible. Most of the remaining labeled cells are Müller cells. Some Müller cells (arrowheads) are seen surrounding unlabeled somata of retinal ganglion cells. Scale bar, 100 μm.

    Journal: Methods in molecular biology (Clifton, N.J.)

    Article Title: Assessment of Glial Function in the In Vivo Retina

    doi: 10.1007/978-1-61779-452-0_33

    Figure Lengend Snippet: Glial cells of the retina. Glial cells (green) are labeled with the Ca2+ indicator dye Oregon Green 488 BAPTA-1 and vessels (orange) by intravenous ejection of dextran rhodamine B isothiocyanate in this confocal image of the retina. Several astrocytes (arrows) are visible. Most of the remaining labeled cells are Müller cells. Some Müller cells (arrowheads) are seen surrounding unlabeled somata of retinal ganglion cells. Scale bar, 100 μm.

    Article Snippet: Blood Vessel Labeling Dextran fluorescein isothiocyanate, 2,000,000 MW (Sigma) dissolved in saline (3% solution).

    Techniques: Labeling

    Glial-evoked dilation of retinal arteriole. (a) Confocal image of the retina, showing OGB-labeled glial cells and an arteriole (a) labeled with dextran rhodamine B isothiocyanate. The luminal diameter of the arteriole is monitored with confocal line scans (the white line across the vessel). Asterisk indicates the site of caged Ca2+ photolysis; scale bar, 25 μm. (b) Glial Ca2+ fluorescence measured near the arteriole. Photolysis of caged Ca2+ evokes a glial Ca2+ increase. (c) The luminal diameter of the arteriole. Photolysis evokes a transient increase in vessel diameter.

    Journal: Methods in molecular biology (Clifton, N.J.)

    Article Title: Assessment of Glial Function in the In Vivo Retina

    doi: 10.1007/978-1-61779-452-0_33

    Figure Lengend Snippet: Glial-evoked dilation of retinal arteriole. (a) Confocal image of the retina, showing OGB-labeled glial cells and an arteriole (a) labeled with dextran rhodamine B isothiocyanate. The luminal diameter of the arteriole is monitored with confocal line scans (the white line across the vessel). Asterisk indicates the site of caged Ca2+ photolysis; scale bar, 25 μm. (b) Glial Ca2+ fluorescence measured near the arteriole. Photolysis of caged Ca2+ evokes a glial Ca2+ increase. (c) The luminal diameter of the arteriole. Photolysis evokes a transient increase in vessel diameter.

    Article Snippet: Blood Vessel Labeling Dextran fluorescein isothiocyanate, 2,000,000 MW (Sigma) dissolved in saline (3% solution).

    Techniques: Labeling, Fluorescence