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xdh xo  (Bio-Techne corporation)


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    Structured Review

    Bio-Techne corporation xdh xo
    Specifications of primary antibodies used for immunofluorescence studies.
    Xdh Xo, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/xdh xo/product/Bio-Techne corporation
    Average 92 stars, based on 2 article reviews
    xdh xo - by Bioz Stars, 2026-03
    92/100 stars

    Images

    1) Product Images from "Studies on the Effects of Hypercholesterolemia on Mouse Ophthalmic Artery Reactivity"

    Article Title: Studies on the Effects of Hypercholesterolemia on Mouse Ophthalmic Artery Reactivity

    Journal: Diseases

    doi: 10.3390/diseases11040124

    Specifications of primary antibodies used for immunofluorescence studies.
    Figure Legend Snippet: Specifications of primary antibodies used for immunofluorescence studies.

    Techniques Used: Immunofluorescence

    Messenger RNA expression for the pro-oxidative redox enzymes NOX1, NOX2, NOX4, and XDH/XO in the aorta ( A ) and the ophthalmic artery ( B ) presented as the fold change (mean ± SE) in ApoE−/− mice versus wild-type controls (aorta: n = 8 per genotype; ophthalmic artery: n = 6 per genotype; *** p < 0.001, ApoE−/− versus wild-type mice).
    Figure Legend Snippet: Messenger RNA expression for the pro-oxidative redox enzymes NOX1, NOX2, NOX4, and XDH/XO in the aorta ( A ) and the ophthalmic artery ( B ) presented as the fold change (mean ± SE) in ApoE−/− mice versus wild-type controls (aorta: n = 8 per genotype; ophthalmic artery: n = 6 per genotype; *** p < 0.001, ApoE−/− versus wild-type mice).

    Techniques Used: RNA Expression

    Immunofluorescence staining for pro-oxidative redox enzymes in aortic tissue sections. Immunoreactivity to NOX1 was markedly elevated in the endothelium of ApoE−/− mice ( A ). Likewise, NOX2 immunoreactivity was pronounced in the ApoE−/− mouse endothelium ( B ). Interestingly, NOX4 immunoreactivity was not elevated in the endothelium, but in the media of ApoE−/− mice ( C ). Immunoreactivity to XDH/XO was weak in both wild-type and ApoE−/− mice ( D ). Data are presented as mean ± SE normalized to wild-type controls (n = 8 per genotype; *** p < 0.001; ** p < 0.01, ApoE−/− versus wild-type mice). The white arrows point to the endothelial layer. Blue: DAPI; Red: Rhodamine Red-X-coupled. Scale bar = 20 µm.
    Figure Legend Snippet: Immunofluorescence staining for pro-oxidative redox enzymes in aortic tissue sections. Immunoreactivity to NOX1 was markedly elevated in the endothelium of ApoE−/− mice ( A ). Likewise, NOX2 immunoreactivity was pronounced in the ApoE−/− mouse endothelium ( B ). Interestingly, NOX4 immunoreactivity was not elevated in the endothelium, but in the media of ApoE−/− mice ( C ). Immunoreactivity to XDH/XO was weak in both wild-type and ApoE−/− mice ( D ). Data are presented as mean ± SE normalized to wild-type controls (n = 8 per genotype; *** p < 0.001; ** p < 0.01, ApoE−/− versus wild-type mice). The white arrows point to the endothelial layer. Blue: DAPI; Red: Rhodamine Red-X-coupled. Scale bar = 20 µm.

    Techniques Used: Immunofluorescence, Staining

    Immunofluorescence staining for pro-oxidative redox enzymes in ophthalmic artery cross-sections. Immunoreactivity to NOX1 ( A ), NOX2 ( B ), and NOX4 ( C ) was negligible in both wild-type and ApoE−/− mice. Only faint immunoreactivity to XDH/XO was visible in the media and adventitia of the ophthalmic artery but was similar in wild-type and ApoE−/− mice ( D ). Data are presented as mean ± SE normalized to wild-type controls (n = 8 per genotype). The white arrows point to the endothelial layer. Blue: DAPI; Red: Rhodamine Red-X-coupled. Scale bar = 20 µm.
    Figure Legend Snippet: Immunofluorescence staining for pro-oxidative redox enzymes in ophthalmic artery cross-sections. Immunoreactivity to NOX1 ( A ), NOX2 ( B ), and NOX4 ( C ) was negligible in both wild-type and ApoE−/− mice. Only faint immunoreactivity to XDH/XO was visible in the media and adventitia of the ophthalmic artery but was similar in wild-type and ApoE−/− mice ( D ). Data are presented as mean ± SE normalized to wild-type controls (n = 8 per genotype). The white arrows point to the endothelial layer. Blue: DAPI; Red: Rhodamine Red-X-coupled. Scale bar = 20 µm.

    Techniques Used: Immunofluorescence, Staining



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    Image Search Results


    Specifications of primary antibodies used for immunofluorescence studies.

    Journal: Diseases

    Article Title: Studies on the Effects of Hypercholesterolemia on Mouse Ophthalmic Artery Reactivity

    doi: 10.3390/diseases11040124

    Figure Lengend Snippet: Specifications of primary antibodies used for immunofluorescence studies.

    Article Snippet: XDH/XO , NBP2-75717, Bio-Techne GmbH, Wiesbaden, Germany , Rabbit, monoclonal , 1:50.

    Techniques: Immunofluorescence

    Messenger RNA expression for the pro-oxidative redox enzymes NOX1, NOX2, NOX4, and XDH/XO in the aorta ( A ) and the ophthalmic artery ( B ) presented as the fold change (mean ± SE) in ApoE−/− mice versus wild-type controls (aorta: n = 8 per genotype; ophthalmic artery: n = 6 per genotype; *** p < 0.001, ApoE−/− versus wild-type mice).

    Journal: Diseases

    Article Title: Studies on the Effects of Hypercholesterolemia on Mouse Ophthalmic Artery Reactivity

    doi: 10.3390/diseases11040124

    Figure Lengend Snippet: Messenger RNA expression for the pro-oxidative redox enzymes NOX1, NOX2, NOX4, and XDH/XO in the aorta ( A ) and the ophthalmic artery ( B ) presented as the fold change (mean ± SE) in ApoE−/− mice versus wild-type controls (aorta: n = 8 per genotype; ophthalmic artery: n = 6 per genotype; *** p < 0.001, ApoE−/− versus wild-type mice).

    Article Snippet: XDH/XO , NBP2-75717, Bio-Techne GmbH, Wiesbaden, Germany , Rabbit, monoclonal , 1:50.

    Techniques: RNA Expression

    Immunofluorescence staining for pro-oxidative redox enzymes in aortic tissue sections. Immunoreactivity to NOX1 was markedly elevated in the endothelium of ApoE−/− mice ( A ). Likewise, NOX2 immunoreactivity was pronounced in the ApoE−/− mouse endothelium ( B ). Interestingly, NOX4 immunoreactivity was not elevated in the endothelium, but in the media of ApoE−/− mice ( C ). Immunoreactivity to XDH/XO was weak in both wild-type and ApoE−/− mice ( D ). Data are presented as mean ± SE normalized to wild-type controls (n = 8 per genotype; *** p < 0.001; ** p < 0.01, ApoE−/− versus wild-type mice). The white arrows point to the endothelial layer. Blue: DAPI; Red: Rhodamine Red-X-coupled. Scale bar = 20 µm.

    Journal: Diseases

    Article Title: Studies on the Effects of Hypercholesterolemia on Mouse Ophthalmic Artery Reactivity

    doi: 10.3390/diseases11040124

    Figure Lengend Snippet: Immunofluorescence staining for pro-oxidative redox enzymes in aortic tissue sections. Immunoreactivity to NOX1 was markedly elevated in the endothelium of ApoE−/− mice ( A ). Likewise, NOX2 immunoreactivity was pronounced in the ApoE−/− mouse endothelium ( B ). Interestingly, NOX4 immunoreactivity was not elevated in the endothelium, but in the media of ApoE−/− mice ( C ). Immunoreactivity to XDH/XO was weak in both wild-type and ApoE−/− mice ( D ). Data are presented as mean ± SE normalized to wild-type controls (n = 8 per genotype; *** p < 0.001; ** p < 0.01, ApoE−/− versus wild-type mice). The white arrows point to the endothelial layer. Blue: DAPI; Red: Rhodamine Red-X-coupled. Scale bar = 20 µm.

    Article Snippet: XDH/XO , NBP2-75717, Bio-Techne GmbH, Wiesbaden, Germany , Rabbit, monoclonal , 1:50.

    Techniques: Immunofluorescence, Staining

    Immunofluorescence staining for pro-oxidative redox enzymes in ophthalmic artery cross-sections. Immunoreactivity to NOX1 ( A ), NOX2 ( B ), and NOX4 ( C ) was negligible in both wild-type and ApoE−/− mice. Only faint immunoreactivity to XDH/XO was visible in the media and adventitia of the ophthalmic artery but was similar in wild-type and ApoE−/− mice ( D ). Data are presented as mean ± SE normalized to wild-type controls (n = 8 per genotype). The white arrows point to the endothelial layer. Blue: DAPI; Red: Rhodamine Red-X-coupled. Scale bar = 20 µm.

    Journal: Diseases

    Article Title: Studies on the Effects of Hypercholesterolemia on Mouse Ophthalmic Artery Reactivity

    doi: 10.3390/diseases11040124

    Figure Lengend Snippet: Immunofluorescence staining for pro-oxidative redox enzymes in ophthalmic artery cross-sections. Immunoreactivity to NOX1 ( A ), NOX2 ( B ), and NOX4 ( C ) was negligible in both wild-type and ApoE−/− mice. Only faint immunoreactivity to XDH/XO was visible in the media and adventitia of the ophthalmic artery but was similar in wild-type and ApoE−/− mice ( D ). Data are presented as mean ± SE normalized to wild-type controls (n = 8 per genotype). The white arrows point to the endothelial layer. Blue: DAPI; Red: Rhodamine Red-X-coupled. Scale bar = 20 µm.

    Article Snippet: XDH/XO , NBP2-75717, Bio-Techne GmbH, Wiesbaden, Germany , Rabbit, monoclonal , 1:50.

    Techniques: Immunofluorescence, Staining