20 November 2020 3 6K Report

I have tissue scaffolds with primary neural cells from rats that have been fixed and stained with PFA, Triton X and then primary antibody Anti-Beta-Tubulin-III antibody from rabbit (sigma T2200) then secondary antibody Anti-fibronectin antibody produced in rabbit (sigma F3648).

I usually wash with PBS following incubation with the secondary antibody and then use a confocal microscope to image. However, the microscope won't be available for a fed days this time (something that was brought to my attention late). Usually I would stop after fixing them to store them but staining is already in progress. Once I remove the secondary antibody how should I store them? It will only be for a few days, do I leave them in PBS in a cold room at (-4 C)? will that wash the stain out?

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