As autophagy is a multi-step process which includes not just the formation of autophagosomes, but most importantly, flux through the entire system, including the degradation upon fusion with lysosomes, which makes it quite challenging for detection. There are several methods for detection in mammalian cells, including immunoblotting analysis of LC3 and p62 and detection of autophagosome formation/maturation by fluorescence microscopy, Currently, there is no single “gold standard” for determining the autophagic activity that is applicable in every experimental context, hence it is recommended to go for the combined use of multiple methods to accurately assess the autophagic activity in any given biological setting.
Get tips on using PI/RNase Staining Buffer to perform Cell cycle assay mouse - C2C12
Get tips on using PI/RNase Staining Buffer to perform Cell cycle assay mouse - L929
As autophagy is a multi-step process which includes not just the formation of autophagosomes, but most importantly, flux through the entire system, including the degradation upon fusion with lysosomes, which makes it quite challenging for detection. There are several methods for detection in mammalian cells, including immunoblotting analysis of LC3 and p62 and detection of autophagosome formation/maturation by fluorescence microscopy, Currently, there is no single “gold standard” for determining the autophagic activity that is applicable in every experimental context, hence it is recommended to go for the combined use of multiple methods to accurately assess the autophagic activity in any given biological setting.
Get tips on using Senescence Cells Histochemical Staining Kit to perform Cell cycle assay mouse - L929
Get tips on using FITC BrdU Flow Kit to perform Cell cycle assay mouse - RAW 264.7
Get tips on using APC BrdU Flow Kit to perform Cell cycle assay mouse - 3T3-L1
Get tips on using FxCycle™ PI/RNase Staining Solution to perform Cell cycle assay mouse - C2C12
Get tips on using FxCycle™ PI/RNase Staining Solution to perform Cell cycle assay mouse - 3T3-L1
A standard angiogenic assay involves the autonomous endothelial cell response of self-organization into microvessels, also known as tubes when seeded on a basement membrane matrix in the presence of the appropriate growth factors. However, the component of basement membrane matrix may also affect the tube formation by endothelial cells. Hence it is important to use a standard angiogenesis assay kit or use the same membrane matrix with known composition to standardize the assay conditions.
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