Discussion of all aspects of cellular structure, physiology and communication.
3 posts • Page 1 of 1
Recently, I used FACS-buffer (PBS, 2 mM EDTA, 25 mM HEPES) for antibody dilution and washing. Although, clump formation was less but it was present. Besides, I would also like to know that do the presence of HEPES buffer and EDTA interfere with the result while making antibody dilution buffer.
Who is online
Users browsing this forum: No registered users and 3 guests