I have cloned xho1 and sal1 restriction sites into a gene and transformed it, i am now trying to check if the insert is there by digesting the extracted plamid after transformation, digesting it with the same 2 enzymes as said before and running on gel. i am used to use the enzymes from roche and there they have same buffer for both so it was easier. Now i have xho1 from roche and sal1 from neb, different companies, different buffers. i know it has to be sequential digestion, but worried about the certainity it would work. anyone done this before, did it work, any advice or suggestions?? thanks a lot in advance.
Edited by student47, 19 September 2013 - 05:07 AM.