Hi! This is probably a stupid question...but what does is the purpose of "quenching" PFA after fixing cells to be analyzed via IF? What is the best quencher when using predominantly FITC and TxR secondary antibodies? How does this process of quenching work?
Thanks!!!
PFA Quenching in Staining of 2D and 3D MDCK Cultures
Started by carlymichelle, Aug 31 2009 09:26 PM
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