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机构地区:[1]军事医学科学院基础医学研究所
出 处:《免疫学杂志》1999年第1期11-13,共3页Immunological Journal
摘 要:设计三条引物P1、P2、P3扩增全长hFas基因和只含有跨膜区和胞浆区的mFas基因。P2上设计一个BstXI位点,以与hFas信号肽之后的单酶切位点BstXI连接,获得带信号肽的跨膜区和胞浆区SpmFas基因。另外设计两条引物P4、P5扩增人β-雌二醇受体的激素结合结构域。扩增基因均经DNA序列分析得到证实。Ρ3、P4均设计了KpnI位点,用于两基因融合,并将此融合基因插入真核表达载体pcDNA3。脂质体法转入COS-7细胞进行瞬时表达,WesternBlot检测到约57KDa的表达产物,与融合基因的估算分子量相符。Three primers P 1、P 2、P 3 were used to amplify the whole sequence and the transmembrane and cytoplasma fraction of hFas by PCR. A BstX I site was designed in P 2 to ligate with the BstX I site downstream hFas signal peptide to obtain SpmFas. Other two primers P 4、P 5 were used to PCR amplify the hormone binding domain of human β estrogen receptor. All amplified fragments were verified by sequencing analysis. The two genes were fused at Kpn I site designed in both P 3 and P 4 and then the fusion gene was inserted into pcDNAs.Using lipofectamine mediated gene transfer technique, the fusion gene was tranduced into COS 7 cells and a 57DKa expression band which is in agreement with the calculated Mr was detected by Westen blot analysis.
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