Aim: To obtain the C-terminal DNA and construct the expression plasmid in yeast two-hybrid. Methods: About 177bp DNA fragment was amplified from the complete sequence of ( receptor by PCR. After being sequenced, the C-terminal fragment was ligased into EcoR I-BamH I site of pGBKT7 vector to form recombinants. The recombinant
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机译:molecular cloning, characterization and expression analysis of tumor necrosis factor receptor-associated factor 3 (TRaF3) from pearl oyster pinctada fucata