Σύγκριση μεθόδων

	Δοκιμασία Live/Dead	CAM Assay
Πεδίο	Βιοϋλικά	Βιοϋλικά
Οικογένεια	Process / pipeline	Process / pipeline
Έτος προέλευσης	2000	1974
Δημιουργός	Invitrogen/Molecular Probes	Judah Folkman
Τύπος	Dual-dye viability assay	Developmental biology assay
Θεμελιώδης πηγή	Molecular Probes (2004). LIVE/DEAD Viability/Cytotoxicity Kit user guide. Invitrogen Corporation.	Folkman, J. (1974). Tumor angiogenesis: therapeutic implications. New England Journal of Medicine, 285(21), 1182-1186.
Εναλλακτικές ονομασίες	calcein-AM/propidium iodide, SYTO/PI staining, fluorescent viability stain	chick embryo chorioallantoic membrane, angiogenesis assay, CAM angiogenesis model
Συναφείς	4	4
Σύνοψη	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.	The 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.