The amplified gene was cloned into the pENTR11 vector. With the pENTR11-SLC plasmid and the backbone plasmid pAd/CMV/V5-DEST, the homologous recombination reaction took place in vitro. The reaction mixture was transferred into TOP10 E.

 
  • 方法采用PCR技術(shù)從含有SLC基因的質(zhì)粒上擴增出SLC基因,將PCR產(chǎn)物酶切后連接至pENTR11載體上,再通過(guò)pENTR11與腺病毒骨架載體pAd/CMV/V5-DEST之間的同源重組作用將SLC基因片段重組至pAd/CMV/V5-DEST上,最后經(jīng)293細胞的包裝擴增后得到攜帶SLC基因的重組腺病毒。
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