引物

传染性法氏囊病病毒的PCR引物设计与Internet检索分析

Design of Infectious Bursal Disease Virus PCR Primer and Internet Retrieval

应用引物延伸预扩增反应技术检测孕妇血浆中的胎儿DNA

Detection of fetal DNA using primer extension preamplification followed by nested PCR

不同对虾种间共用微卫星DNA引物的研究

Common Microsatellite Primers for Molecular Markers in Different Shrimp Species

DNA引物酶抑制剂筛选方法的建立及应用

The establishment of a screening method of DNA primase inhibitors

单引物PCR扩增DNA指纹图谱的稳定性研究

Studies on constancy of DNA fingerprints amplified by single - primed PCR

单引物PCR扩增的DNA分子模式

DNA molecular models of PCR amplification by single primers

几种引物对苏铁共生蓝细菌的DNA多态性分析

DNA diversity analysis on the Cyanobacteria freshly isolated from Cycads based on PCR with different primers

鸡品种随机引物扩增多态DNA的研究

Study of RAPD on fowls breeds

随机引物扩增DNA多态性技术在分析金黄色葡萄球菌和肺炎杆菌多态性中的应用

Application of randomly amplified polymorphic DNA on the DNA polymorphism of Staphylococcus aureus and Klebsiella pneumoniae

利用9个随机引物对四川省18个骨干恢复系进行了DNA多态性分析。

The RAPD analysis was conducted on 18 restorer lines of Sichuan Province with 9 random primers .

由此进行单引物PCR扩增，它们的扩增产物形成了稳定的引物&模板特异的DNA指纹图谱。

The products amplified by single-primed PCR formed DNA fingerprints with the specificity of primer-template .

随机引物PCR技术在个体认定及亲权鉴定中的应用

The application of AP-PCR on paternity testing and identification

设计引物，进行PCR，测序结果与电子克隆结果完全一致，证明克隆成功。

The sequencing result confirms the success of e-clone .

毛豹皮樟的叶片DNA提取及其RAPD引物筛选

DNA Extraction and RAPD Primer Screening in Leaves of Litsea coreana var. lanuginosa

方法用一对引物进行PCR扩增，扩增产物纯化后用双脱氧终止法测序。

The PCR products were purified and sequenced by the methods of Sanger dideoxy .

通用引物PCR检测临床常见致病菌的实验研究

Universal Primer PCR for Detection of Clinic Bacteria

离子束介导任意引物PCR差异片段转化在育种中的可行性及前景

The Feasibility and Prospects in the Breeding of Transferring Differential Fragments by Ion Beam

PCR在阴道毛滴虫检测中的引物筛选和条件优化

Optimization of PCR Components and Selection of Its Primers for Detection of Trichomonas Vaginalis

选用6个叶绿体和4个线粒体植物细胞质通用引物，以所有材料基因组DNA进行筛选。

Genomic DNAs from all the samples were amplified with cytoplasm universal primers of 6 chloroplast and 4 mitochondrial .

所以使用这两对引物进行两次PCR反应可将目标菌Cur。

By using these two primer pairs and two times of PCR protocols , Cur .

用巢式PCR、引物延伸预扩增法扩增单细胞，扩增率分别为90%和85%。

Amplification rate of nest-PCR and PEP was 90 % and 85 % , respectively .

重叠延伸PCR技术成功的关键是重叠互补引物的设计。

The overlap primers design is the key factor for the successful accomplishment of SOE PCR .

选择编码EHV－1和EHV－4的糖蛋白B（gB）基因作为引物。

Primers were chosen from the glycoprotein B ( gB ) coding region of each serotype .

b孢子蚕卵、蚕蛾的模板DNA制备方法的基础上，选用MP1/MP2和V1F/530R两对引物进行PCR扩增检测。

B , and two sets of primer V1F / 530R and MP1 / MP2 were selected for PCR diagnosis .

提取地衣芽孢杆菌的染色体DNA，设计合适引物，运用PCR法扩增得到了耐高温α-淀粉酶基因，并将其克隆在大肠杆菌中。

The heat-stable α - amylase gene was amplified from B. licheniformis with PCR and cloned in Escherichia coli .

同源引物差示PCR方法的建立及胎肝特异表达基因的差示筛选

Development of Analogy Primer-mediated Differential Display-PCR and Identification of New Genes Differentially Expressed in Human Fetal Liver

RT－PCR试剂盒为hkaa产品，引物均由北京奥科公司合成。

RT-PCR kit was obtained from Takara Company .

平均每对引物组合扩增的DNA带数为66.13，总的多态性比率为78.84%。

The average number of DNA band produced by each primer combination was 66.13 and the total polymorphic rate was 78.84 % .

根瘤菌RAPD引物筛选及条件优化

Optimization and primers screening of RAPD Reaction System for Rhizobia

目前主要是利用简并引物PCR技术和分子图谱法分离植物抗病基因。

The main methods for cloning resistance gene to diseases cover degenerate primer PCR and molecular mapping method .