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1.Results: hIL-2 DNA frag- ment from pLXSN with EcoRI-BamH Ⅰ restriction enzymes digest was successfully cloned to pBluescript ⅡSK+/-.
结果:克隆有hIL-2基因的pLXSN经EcoRI-BamHI酶切后,hIL-2基因被成功地连接到质粒pBluescriptⅡSK+/-上,再经Sail-BamHI酶切后,hIL-2基因又被克隆到pMJ601真核表达载体上。收藏指正
2.Results 1. The result of restriction enzyme digest and gene sequence showed that the EWS-FLI-1 binding sequence (ACCGGAAGT) lay at the upper stream of diphtheria toxin A fragment.
结果 1、对重组载体的酶切鉴定和测序结果证实,在pS2-DTA中EWS-FLI-1特异性结合序列(ACCGGAAGT)位于白喉毒素A链基因上游。收藏指正
3.PCR-RFLPs of the ITS region of 11 intra-populations of soybean cyst forming nematodes were made with five restriction enzymes. Four of which, Alu I, Cfo I , Rsa I and Mva I , produced the same digest pattern among all the 11 populations.
RFLPs分析表明:经AluⅠ,CfoⅠ,RsaⅠ及MvaⅠ等酶切后,各大豆胞囊线虫群体均得到了相同的酶切图谱。收藏指正
4.Methods Digest plasmid pSFV-MCS with restriction endonuclease,and insert the obtained SFV replicon into vector pIRESneo containing CMV promoter and enhancer to construct a novel eukaryotic expression vector pCS. Insert HIV-1 MEGp24 gene into vector pCS,then transfect the constructed recombinant DNA vaccine pCS-MEGp24 to BHK-21 cells in mediation of liposome.
方法将含SFV复制子的元件从pSFV-MCS中切下,连入含CMV启动子及增强子的pIRESneo载体中,构建新型真核表达载体pCS,再将含HIV-1 MEGp24基因插入至pCS载体中,构建重组核酸疫苗pCS-MEGp24。收藏指正
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