I tried to digest my pBSK(-) vector with EcoRV but failed. No linearized vector band on my agarose gel, just supercoiled + circular (nicked) DNA. I used 20 units of newly bought enzyme in the appropriate buffer + BSA, digested for 3 h at 37 degrees - should be more than sufficient. The vector is easily and completely digested by HaeIII in 1h. If the vector DNA from a Maxi-Prep is poor quality, it shouldn´t be digested by HaeIII either, right? Methylation shouldn´t be a problem for EcoRV.
Anybody having an idea?
Submit your paper to J Biol Methods today!
1 reply to this topic