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| DNA Techniques Post questions and discuss DNA techniques and protocols such as DNA extraction, PCR, and the study of DNA-binding proteins. |
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| I need to seqeunce my two DNA in pGEX-2t vector in BL21 cells. I tried to mini prep and Maxiprep however the DNA conc is too low to sequence. Is there any way I can increase DNA amount? I usually use 1ml culture for miniprep or 50ml culture for maxiprep. Please, help me. Last edited by david1259; 02-12-2008 at 07:27 PM. |
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| 1) I would not suggest using BL21 cells to propagate plasmids. They're not as good as DH5a (for example) at avoiding DNA recombination and mutation issues. 2) I use 5 mL of culture for a miniprep and 50 for a midiprep -- for high copy plasmids, the Qiagen maxi kits take 100 mL of culture. You could try scaling up. 3) If it's simply a concentration issue rather than yield, an ethanol precipitation step will give you higher concentration plasmid. |
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