Discussion of all aspects of biological molecules, biochemical processes and laboratory procedures in the field.
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I tried to transform JM 109 with pGEM-T vector (w/ inserts). But when I plated them on LB/Amp/X-Gal/IPTG, there were only 3-4 colonies of each blue and clear colonies coming out. Wondering what has happened. Will it be the ligation problem or JM109? I did positive control and it comes out ok. Does anyone experience this? Thanks in advance.
I did an experiment before involving restriction digestion, ligation and transformation and I had expected many colonies to form but only 1 did. Then my mentor told me (after much thinking) that this most probably occured because the restriction enzyme I used was very inefficient and may not have cut the vector - so only 1 colony formed. So now, I am increasing the amount of the restriction enzyme and I hope that I get many colonies once I transform them.
Botany is the study of what? Bottoms!
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