I digested the vectors(pCR4-TOPO and pcDNA3 - from Invitrogen) with EcoRI and performed an in-gel ligation. Though after transforming DH5Alphas, next day i get up to 100 very very small colonies, which i am unable to grow in a selective medium. (control plate was negative). Can anyone help me?
THX
Subcloning problem
Started by ZaPHoD, Jul 17 2002 03:32 AM
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