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1)  single-tube bi-directional allele specific amplification
单管双向等位基因特异扩增
1.
Genotyping was analysed by enzyme cutting, single-tube bi-directional allele specific amplification (SB-ASA) and Snap-shot between the normal people and 2-DM patients.
方法 采用双向测序和Polyphred软件,寻找单核苷酸多态性(SNP),对75~96份2-DM病人和75~96份正常人进行酶切、单管双向等位基因特异扩增和单碱基延伸反应进行基因分型及统计分析。
2)  Bidirectional PCR amplification of specific alleles (Bi PASA)
双向PCR扩增特异等位基因(Bi-PASA)
3)  bi-directional allele-specific amplification
双向等位基因特异性扩增
4)  Allele-specific amplification
等位基因特异扩增法
1.
Objective:To establish Allele-specific amplification(ASA-PCR)for study the distribution of MDR1 polymorphism in transplant patients.
目的:建立等位基因特异扩增法(Allele-Specific Amplification,ASA-PCR)研究移植患者多药耐药基因(multi-drug re- sistance gene,MDR1)多态性。
5)  allele specific amplification
等位基因特异性扩增
1.
[Methods] A total of 100 healthy Liaoning Hans were studied by the use of PCR and allele specific amplification (ASA) techniques.
方法用聚合酶链反应及等位基因特异性扩增技术对100名辽宁地区汉族人的DRD4基因启动子区3个多态性进行了检测,并与其他人群做了比较。
6)  Allele specific amplification
等位基因特异扩增
1.
Allele specific amplification (ASA) is a low-cost, robust technique that can be utilized to discriminate between the all.
本试验通过等位基因特异扩增(ASA)方法对9个香稻和3个非香稻品种(品系),以及3个香稻/非香稻组合的F1的香味基因,进行快速检测。
补充资料:等位
1.官阶爵位。
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