1)NcSRS2 geneNcSRS2基因
1.Subcloning and expression of the NcSRS2 gene fragment of Neospora caninum;新孢子虫NcSRS2基因的亚克隆和表达
2.The NcSRS2 gene fragment of Neospora caninum was amplified from pMD18-NcSRS2 by PCR,and then inserte into the pGEX-4T-2 vector.以含有犬新孢子虫NcSRS2基因的质粒pMD18-NcSRS2为模板,应用PCR方法扩增Nc-SRS2基因,将该基因片段克隆至原核表达载体pGEX-4T-2,构建了重组表达质粒pGEX-Nc-SRS2,转化大肠杆菌BL21中并诱导表达。
3.Based on the NcSRS2 gene sequence of Neospora caninum in the Genbank,a pair of primers containing EcoRⅠand NotⅠenyme digestion sites were designed.根据已发表的犬新孢子虫NcSRS2基因序列,设计1对含有EcoRⅠ和NotⅠ酶切位点的引物。
英文短句/例句
1.Epidemiological Study of Neospora Caninum Infections in Abortion Dairy Cattle of Xinjiang Region and Construction of Prokaryotic Expression Plasmid of NcSRS2 Gene新疆地区流产奶牛新孢子虫病流行病学研究及NcSRS2基因原核表达载体的构建
2.Neospora Caninum Major Surface Proteins, NcSRS2 and NcSAG1, and the Immunogenicity of Recombinant Proteins;新孢子虫NcSRS2和NcSAG1基因及重组蛋白免疫原性的研究
3.Studies on NcSRS2 DNA Vaccine of Neospora Caninum;新孢子虫NcSRS2 DNA疫苗的研究
4.extinguisher loci消失基因座，绝灭基因座
5.Of, relating to, produced by, or being genes or a gene.基因的基因的，与基因有关的，基因产生的
6.Genes are described as DOMINANT or RECESSIVE.基因分为显性基因和隐性基因。
7.hypomorphic allele次等位因素对偶基因
8.Studies on Polymorphism of Prolactin Receptor Gene and Follicle-Stimulating Hormone Beta Subunit Gene in Swine;猪PRLR基因和FSHβ亚基基因多态性研究
9.Research on Hte Microarray Based Gene Mining Algorithm;基于基因表达谱的基因挖掘算法研究
10.Human Genome Project,Post-genome Research and Gene Medicine --New Century of Diagnosis,Pharmaceutics and Therapy with Gene Technique;人类基因组计划、后基因组研究与基因医学——基因诊断、基因制药与基因治疗的新世纪
11.Genetic material produced by gene-splicing.重组基因材料基因分割而产生的基因材料
12.Gene distribution was out of balance. Dominant genes were more than recessive ones.基因的分布是不对称的,显性基因多于隐性基因。
13.Association of apoE Gene, A2M Gene and ACE Gene Polymorphism with Alzheimer s Disease;apoE基因、A2M基因、ACE基因与汉人Alzheimer病的相关性研究
14.Study on Inheritance of the Quality Transgenes Over-expressed in Transgenic Wheat;转基因小麦外源基因品质基因表达的遗传研究
15.Legal Research on Gene Science and Technology--Does Gene Belong to Invention or Discovery;基因科技的法律问题研究——“发明”基因?“发现”基因?
16.Mapping of Genetic Modifiers of Eyal~(bor/bor) Mice定位Eyal~(bor/bor)基因型小鼠Eyal基因的遗传修饰基因
17.Analyses of Genome-wide Disease Resistance Genes and Their Expansion in Medicago truncatula蒺藜苜蓿全基因组抗病基因和基因扩张分析
18.ADP ribosylation factorADP核糖基化因子
相关短句/例句
gene[英][d?i:n][美][d?in]基因
1.Study of the Preparation and the Characteristics of pRc/CMV-BChE Gene-chitosan nanoparticles ①;丁酰胆碱酯酶基因-壳聚糖纳米粒初步研究
2.Correlation between traditional Chinese medicine syndromes in primary immunoglobulin A nephropathy and A267G in 5'-untranslated region within exonal of megsin gene;Megsin基因E1-5’UTR区A267G与免疫球蛋白A型肾病阴虚证的相关性
3.Study on gene chip of leiomyoma of uterus;子宫肌瘤基因芯片的研究
3)Genes基因
1.Study on Apoptosis of Human Leukemia Cells and Its Related Genes Regulation Induced by ~(235) U;浓缩铀诱发细胞凋亡的形态及基因调控
2.Screening of lymphatic metastasis-associated genes in esophageal squamous cell carcinoma;食管癌淋巴结转移相关基因筛选的研究
3.Study on the Genotyping of Aminoglycoside Modifying Enzymes Genes from Pan-drug Resistant Acinetobacter Baumannii.;泛耐药鲍曼不动杆菌氨基糖苷类修饰酶基因研究
4)Polymorphism[英][,p?li'm?:fiz?m][美][,pɑl?'m?rf?zm?]基因
1.The Study on Apolipoprotein E Gene Polymorphism Characteristics of Cerebral Infarction and Intracerebral Hemorrhage;脑梗死与脑出血apoE-基因多态性特点研究
2.The Relations of Gene Polymorphisms of eNOS and FⅦ with Coronary Heart Disease in Henan Han Population;河南汉族人群一氧化氮合酶和凝血因子Ⅶ基因多态性与冠心病相关性分析
3.Methods:Polymorphism of the 677th site C/T of MTHFR gene and the 66th site A/G of MTRR gene were detected by polymerase chain reaction-restrction fragment length polymorphism in disease group(n=64) and normal controls(n=104).目的:研究同型半胱氨酸相关酶中亚甲基四氢叶酸还原酶(MTHFR)及蛋氨酸合成酶还原酶(MTRR)基因的多态性与先天神经管缺陷的关系。
5)AS geneAS基因
6)Genetic[英][d??'net?k][美][d??'n?t?k]基因
1.Antigenic and genetic characterization of A/Shenzhen/1/99(H3N2) virus;A/深圳/1/99(H3N2)病毒抗原性及基因特性研究
2.Relationship between the genetic polymorphisms of VDR and susceptibility to pulmonary tuberculosis among the Chinese Han population维生素D受体基因多态性与汉族人肺结核发病的关系
3.MTHER genetic C677T polymorphisms were determined by PCR-RFLP.N5, 10 亚甲基四氢叶酸还原酶(MTHFR)是参与甲硫氨酸-叶酸代谢的关键酶,其基因677位点C→T错义突变可造成此酶活性降低,导致高同型半胱氨酸血症,现已证明高同型半胱氨酸是诱发胎儿出生缺陷和心血管疾病的一个独立危险因素。
延伸阅读
J基因分子式：CAS号：性质：为免疫球蛋白V区与C区之间的连接区(J区)编码的基因。
