proteome profiler human angiogenesis array kit (R&D Systems)
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![Mediators of <t>angiogenesis</t> are dysregulated in early-stage/intermediate pathology Alzheimer's disease. ( A and B ) Levels of endoglin (CD105), a marker of neoangiogenesis, measured first using the angiogenesis <t>proteome</t> profiler and then independently by commercial ELISA kit. Mean and standard error of the mean are shown. * P < 0.05, ** P < 0.01. ( C and D ) Levels of pro-angiogenic ( C ) and anti-angiogenic ( D ) mediators in early-stage/intermediate pathology [Braak tangle stage (BS) III–IV] (blue) and late-stage AD (BSV–VI) (red), relative to the levels in minimal pathology BS0–II cases.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_8453/pmc13058453/pmc13058453__awaf394f5.jpg)
Proteome Profiler Human Angiogenesis Array Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 354 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+angiogenesis+array+kit/Proteome+Profiler+Human+Angiogenesis+Array+Kit/pmc13058453-128-9-18
Average 96 stars, based on 354 article reviews
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1) Product Images from "Post-mortem evidence of pathogenic angiogenesis and abnormal vascular function in early Alzheimer’s disease"
Article Title: Post-mortem evidence of pathogenic angiogenesis and abnormal vascular function in early Alzheimer’s disease
Journal: Brain
doi: 10.1093/brain/awaf394
Figure Legend Snippet: Mediators of angiogenesis are dysregulated in early-stage/intermediate pathology Alzheimer's disease. ( A and B ) Levels of endoglin (CD105), a marker of neoangiogenesis, measured first using the angiogenesis proteome profiler and then independently by commercial ELISA kit. Mean and standard error of the mean are shown. * P < 0.05, ** P < 0.01. ( C and D ) Levels of pro-angiogenic ( C ) and anti-angiogenic ( D ) mediators in early-stage/intermediate pathology [Braak tangle stage (BS) III–IV] (blue) and late-stage AD (BSV–VI) (red), relative to the levels in minimal pathology BS0–II cases.
Techniques Used: Marker, Enzyme-linked Immunosorbent Assay
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