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Re: [ccp4bb] problem in transformation of pqe 30 clone |
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- Protein crystallographyMain steps:- Protein purification- Crystallisation Special:- Programs for crystallography- X-ray detectors Basic tutorials:- Chemistry- Protein - Peptide - Amino Acids Xtal community:- CCP4BB |
CCP4bb navigationCCP4bb <-- 1999 <-- November 1999 <-- 30 November 1999Subject: Re: problem in transformation of pqe 30 clone From: Ho-Leung Ng holeung {- at -} BERKELEY {- dot -} EDU Date: 2009-05-04 Hello Artem, We express almost all our proteins in BL21 derivatives. It sounds like you've worked with many proteins that express/behave better in XL1-Blue? ho UC Berkeley ------------------------------------------------------------------------------------------------- XL1-Blue is a strain of E. coli. Whether it is or isn't an expression host depends on the definition, and I am not going to argue semantics. The T5 promoter works with regular garden variety RNApol of E. coli. Therefore ANY E. coli strain is an 'expression host' for vectors that contain this promoter. I've expressed many proteins in XL1-Blue and I see no reason why you can't express yours, either. Artem CCP4bb navigationCCP4bb <-- 1999 <-- November 1999 <-- 30 November 1999 |
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