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 Human VE Cadherin ELISA Kit (ab210968) to perform ELISA Human - VE Cadherin
Get tips on using Human VE-Cadherin Quantikine ELISA Kit to perform ELISA Human - VE Cadherin
Get tips on using Human TNF alpha ELISA Kit (ab181421) to perform ELISA Human - TNF-alpha
Get tips on using Human TNF-alpha Quantikine ELISA Kit to perform ELISA Human - TNF-alpha
Get tips on using Human PDGF BB ELISA Kit (ab100624) to perform ELISA Human - PDGF-BB
Get tips on using Human HO 1 ELISA Kit (ab133064) to perform ELISA Human - HO-1
Get tips on using Human Dkk-1 ELISA Kit (RAB0143) to perform ELISA Human - Dkk-1
Get tips on using Human Dkk-1 DuoSet ELISA (DY1906) to perform ELISA Human - Dkk-1
Get tips on using Human Cytochrome c Quantikine ELISA Kit to perform ELISA Human - Cytochrome C
Fill out your contact details and receive price quotes in your Inbox
Outsource experiment