1) L-meq gene
L-meq基因
1.
Expression and preparation of polyclonal antibody of L-meq gene of Marek′s disease virus;
马立克氏病病毒L-meq基因的原核表达及多克隆抗体的制备
2.
Objective To study the influence of L-meq gene on transcription level of p53 mRNA in chicken embryo fibroblast (CEF)in latent period of Marek disease and explore the relationship between L-meq gene and telomerase activity.
目的研究鸡马立克病(MD)潜伏期L-meq基因对鸡胚成纤维细胞(Chicken embryo fibroblast,CEF)p53mRNA转录水平的影响,并探讨L-meq基因与端粒酶活性的关系。
3.
To characterize the properties and functions of L-meq gene,recombinant eukaryon expression vector pcDNA3.
1(+)-L-meq,利用脂质体2000转染MDCC-MSB1细胞,采用改进的端粒重复序列扩增程序(telomere repeat amplification protocol,TRAP)法、实时荧光定量RT-PCR方法检测转染前后端粒酶活性以及端粒酶反转录酶(telomerase reverse transcriptase,chTERT)chTERT mRNA的表达量的变化,探讨L-meq基因对细胞端粒酶活性的影响。
2) Meq gene
Meq基因
1.
Effect on expression of p53 gene in chicken embryo fibroblasts by MDV meq gene;
鸡MDV meq基因对鸡胚成纤维细胞p53基因表达的影响
2.
In this paper, based on the published sequence of Meq gene of GA strain of MDV, a pair of primers were designed and synthesized.
根据鸡马立克氏病病毒(MDV)GA株Meq基因序列,设计并合成一对用于扩增Meq基因的引物,利用这对引物通过PCR方法分别扩增4株东北地区分离的强毒株、国内标准强毒株J-1株、国内疫苗株814株的Meq基因片段,进行克隆测序,对4株MDV分离毒株Meq基因与国内传统毒株Meq基因及GenBank上收录的国内外9株毒株Meq基因序列进行比较分析。
3.
chTERT and chTR expression level in chicken embryo fibroblasts(CEF) were detected by Real-time relatively quantitative PCR method which was transfected by meq gene,through the TaqMan quantitative testing technique and the telomerase activity was detected with TRAP method and cell cycle changes also detected by flow cytometer.
利用TaqMan探针技术,采用实时荧光相对定量RT-PCR方法检测了MDV中meq基因对鸡胚成纤维细胞(CEF)的端粒酶催化亚单位基因(chTERT)、端粒酶RNA亚基(chTR)表达水平的影响,并用TRAP法测定了端粒酶活性,用流式细胞仪检测了细胞周期的变化。
3) oncogene/meq
致瘤基因/meq基因
4) L gene
L基因
1.
Inhibition of Newcastle disease virus replication by RNA interference targeted to L gene functional region;
靶向新城疫病毒L基因(功能区)的siRNA抑制新城疫病毒的复制
2.
Construction of eukaryotic expressing vectors of L gene of foot-and-mouth disease virus;
口蹄疫病毒L基因真核表达载体的构建及表达
3.
Cloning and sequence analysis of L gene of three Newcastle disease virus isolates in Guangxi;
3株新城疫病毒广西分离株L基因的克隆与序列分析
5) L-FABP gene
L-FABP基因
1.
The results showed:intercomparison sequence from Exonl to part Intronl fragment amplification by primers 1 of two individual selection from each swinery with pig L-FABP gene sequence published in GenBank,found that base site of 237、258、315 .
本研究选用杜洛克、长白、大白、冀合白A、冀合白B、辽宁黑猪、丹育黑猪7个猪群共281头猪为研究对象,利用GenBank上已发表的猪(DQ182323)的L-FABP基因序列设计引物,进行PCR扩增并测序。
补充资料：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。
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。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条