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Phân tích CAM×Phép thử Sống/Chết×
Lĩnh vựcVật liệu sinh họcVật liệu sinh học
HọProcess / pipelineProcess / pipeline
Năm ra đời19742000
Người khởi xướngJudah FolkmanInvitrogen/Molecular Probes
LoạiDevelopmental biology assayDual-dye viability assay
Công trình gốcFolkman, J. (1974). Tumor angiogenesis: therapeutic implications. New England Journal of Medicine, 285(21), 1182-1186. link ↗Molecular Probes (2004). LIVE/DEAD Viability/Cytotoxicity Kit user guide. Invitrogen Corporation. link ↗
Tên gọi khácchick embryo chorioallantoic membrane, angiogenesis assay, CAM angiogenesis modelcalcein-AM/propidium iodide, SYTO/PI staining, fluorescent viability stain
Liên quan44
Tóm tắtThe chorioallantoic membrane (CAM) assay is a well-established in vivo model for studying angiogenesis (new blood vessel formation) and evaluating the pro- or anti-angiogenic properties of biomaterials, drugs, and bioactive molecules. Developed by Judah Folkman in the 1970s, the assay uses the highly vascularized CAM of developing chick embryos as a platform for implanting test materials and observing vascular response. The CAM provides a transparent, immunologically naive microenvironment with rapid and reproducible neovascularization, making it ideal for screening angiogenic potential and assessing biomaterial biocompatibility.The Live/Dead assay is a fluorescence-based method for simultaneously identifying live and dead cells using two complementary dyes. The assay combines calcein-AM (or SYTO fluorophores), which generates bright green fluorescence in living cells with intact esterase activity, with propidium iodide (PI), which produces red fluorescence in dead cells with compromised membrane integrity. Commercially developed by Molecular Probes and now part of Thermo Fisher's portfolio, the Live/Dead kit is widely used to evaluate cell viability on biomaterial scaffolds, in tissue constructs, and following drug or toxin exposure.
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