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克隆与表达
    Objective To clone and express the horseradish peroxidase isozyme C3 gene.
    目的克隆与表达辣根过氧化物酶同功酶C3基因。
    Objective: To clone and express human and rat glial cell linederived neurotrophic factor (GDNF) cDNA.
    目的:克隆与表达人及大鼠胶质细胞源性神经营养因子(GDNF)cDNA。
    Objective To clone and express the E2 gene in envelope region of hepatitis C virus and detect the anti E2 in sera of patients with HCV infection,using the purified E2 Protein.
    目的 对丙型肝炎病毒 (HCV)包膜区E2基因进行克隆与表达 ,并将纯化的E2蛋白用于对HCV感染者血清中E2抗体的检测。
    Objective:To clone and express the gene of α-toxin from Clostridium perfringens(CPa).
    目的 :实现产气荚膜梭菌α毒素 (Clostridiumperfringensalphatoxin ,CPa)基因的克隆与表达
    Objective To clone and express the CD158b gene.
    目的 :CD1 5 8b基因克隆与表达
    Objective:To clone and express the horseradish peroxidase isozyme C3(HRPC3) gene.
    目的:克隆与表达辣根过氧化物酶同功酶C3(HRPC3)基因。
    Objective To clone and express the fused gene fragment coding rhoptry protein ROP2 and major surface protein P30 from Toxoplasma gondii as a preparation for the construction of the complex ROP2,P30 antigen by gene engineering. Methods The gene fragment encoding P30 was amplified by PCR from T.
    目的进行弓形虫棒状体蛋白2(ROP2)和膜表面蛋白1(P30)融合基因的克隆与表达,为弓形虫ROP2-P30基因工程复合抗原的制备做准备。
    Objective To clone and express the pyruvate decarboxylase(PDCzm) from Zymomonas mobilis.
    目的克隆与表达移动单孢菌(Zymomonas mobilis)丙酮酸脱羧酶(Pyruvate decarboxylase,PDC)基因。
    Study on clone and express endothelial nitric oxide synthase traffic inducer protein
    内皮型一氧化氮合酶运输诱导物NOSTRIN基因的克隆与表达
    Purpose of this study is clone and express Trehalose-6-phosphate phosphatase(TPS1) gene by gene engineering, which will be foundation of gene-engineering strain construction further. So main goal of this study is build a high efficient vector that can express the TPS1 in Eco li. strain.
    本研究旨在利用基因工程技术,研究磷酸-6-海藻糖合酶(TPS1)基因在大肠杆茵中的克隆与表达,对进一步构建海藻糖的高产基因工程菌株打下基础,所以本研究的主要目标就是,构建一个包含强启动子的高效表达载体,使磷酸-6-海藻糖合酶基因在大肠杆菌中高效表达。
    The objects of the study are to clone and express the gene fragments encoding the OmpA and OmpB of SFG rickettsiae and to analyze the antigenicities of the recombinant OmpA and OmpB.The gene fragments encoding partial OmpB and OmpA were amplified by PCR from the genomic DNAs of R. rickettsii and R. heilongjiangii, respectively.
    本研究旨在克隆与表达斑点热立克次体的ompA和ompB部分基因片段,并对所表达的重组蛋白的抗原性进行研究。
    Objective:To clone and express the new angiogenesis inhibitor,arresten.
    目的 :克隆与表达arresten ;
    Objectives:To clone and express the S-adenosyl-L-methionine synthetase gene.
    目的:克隆与表达大肠杆菌S-腺苷甲硫氨酸合成酶的基因。
 

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