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pRH2.2 plasmid vector质粒载体
Each Fab clone with A450 signal above 0.2(four times the average background level of the assay) was sequenced;unique Fabs were subcloned into pSVF4 or pRH2.2 vectors,and purified as described above. In total 16 unique Fab sequenceswere obtained from total of 192 single colonies screened: nine Fabs fromlibrary sorting with CaCl2 and seven Fabs from library sorting with EGTA.
Supplier来源:BioVector NTCC Inc.
TEL电话:+86-010-53513060
Website网址: http://www.biovector.net
Each Fab clone with A450 signal above 0.2(four times the average background level of the assay) was sequenced;unique Fabs were subcloned into pSVF4 or pRH2.2 vectors,and purified as described above. In total 16 unique Fab sequenceswere obtained from total of 192 single colonies screened: nine Fabs fromlibrary sorting with CaCl2 and seven Fabs from library sorting with EGTA.
Supplier来源:BioVector NTCC Inc.
TEL电话:+86-010-53513060
Website网址: http://www.biovector.net
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