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| I will be running qPCR using identical, unchanging quantities of forward and reverse primers over a period of time. I'd like to make primer aliquots with the FW and REV primers in the same tube, as this would simplify my qPCR setup. Is there any reason I should keep the FW and REV primers separate for storage purposes? I thought for a moment that this would be conducive to primer-dimer formation, and then recalled that everything should be denatured anyway in the beginning of my qPCR. But hearing someone agree with me would be nice. ![]() Last edited by jcosborn06; 03-14-2008 at 09:41 PM. |
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