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3 votes
1 answer
2k views

Problem with bacterial transformation with electroporation

I have a problem with a bacterial transformation of a yeast gene that I can not solve. I isolated yeast DNA and did a PCR to get my product. I am using pCGCUm vector with a GFP construct. I digest ...
MartinK's user avatar
  • 338
1 vote
1 answer
117 views

How can I improve efficiency of Ecoli transformation?

I am an intern in biology institute. I have a 17.3kbp plasmid need to transform to Ecoli. But I have tried many time but have no or very few colony on LB plate. I know large plasmid have less ...
orange's user avatar
  • 11
0 votes
1 answer
33 views

I accidentally plated DH5a E. coli and left them in the 4℃ for 12 hours, if I put them into the 37℃ incubator will they start growing?

I started ligation of my constructs late last night and was super tired, since I used all of my ligation mixture I would rather not have to re-ligate. I did my transformation procedure as follows: ...
vdg's user avatar
  • 19