2) prokaryotic expression
原核表达
1.
Prokaryotic expression and purification of truncated Rab8 recombinant protein and preparation of polyclonal antibody against Rab8;
重组Rab8截短体蛋白的原核表达、纯化和抗体制备
2.
Prokaryotic expression,purification and primary bio-chemical properties research for Tnfrsf11b N-terminal protein of homo sapiens;
人Tnfrsf11b-N端多肽的原核表达、纯化及其初步分析
3.
Prokaryotic expression and identification of recombinant swine hepatitis E virus ORF2 main antigen region;
重组猪戊型肝炎病毒ORF2区主要抗原域的原核表达及鉴定
3) procaryotic expression
原核表达
1.
Cloning and procaryotic expression of the dehydrin dhn4 gene from Tibetan hulless barley;
青稞脱水素基因dhn4的克隆与原核表达
2.
Cloning and Procaryotic Expression of Gene of Retinol-Binding Protein;
维生素A结合蛋白基因的克隆及原核表达
3.
The procaryotic expression vector PKENG-M for GFP: CMV MP was constructed by cloning in pKEN.
采用重组－ＰＣＲ方法，扩增获得绿色荧光蛋白（ＧＦＰ）与黄瓜花叶病毒运动蛋白（ＣＭＶ ＭＰ）融合基因，将其克隆到 ｐＫＥＮ上，构建了该融合基因的原核表达载体 ｐＫＥＮＧ－Ｍ。
4) expression
[英][ɪk'spreʃn] [美][ɪk'sprɛʃən]
原核表达
1.
Prokaryotic Expression and Purification of Human Heat Shock Protein 70;
人热休克蛋白70的原核表达和纯化的实验研究
2.
Expression and Activity Determination of M Protein Epitopes of SARS Coronavirus;
SARS冠状病毒M蛋白B细胞抗原表位的原核表达与抗原活性检测
3.
Cloning and prokaryotic expression of the N-terminal fragment of mouse long type peptidoglycan recognition protein (mPGRP-L);
小鼠PGRP-L分子N端基因片段的克隆与原核表达
5) Surface antigen
表面抗原
1.
Immunogenicity of N-and C-terminal recombinant protein of 120×10~(3) surface antigen from Rickettsia prowazekii;
普氏立克次体120×10~3表面抗原的N端和C端重组蛋白免疫原性的研究
2.
Expression of surface antigen gene p1 fused with hspB of Coxiella burnetii in E.coli;
贝氏柯克斯体表面抗原基因p1与hspB的融合基因在大肠杆菌中的表达
3.
Cloning and expression of gene fragment encoding the N region of 120kDa surface antigen of Rickettsia prowazekii in E.coli.;
普氏立克次体120kDa表面抗原N段基因的克隆与表达
6) Prokaryote expression
原核表达
1.
It was cloned into the prokaryote expression vector pGEX-6p-1 and obtained recombinant plasmid pGEX-ompmH.
根据禽巴氏杆菌5:A C48-1株OmpH全长基因序列设计一对特异性引物,经PCR扩增获得成熟外膜蛋白H基因(OmpmH),将OmpmH片段非定向插入原核表达载体pGEX-6p-1中,构建重组表达质粒pGEX-OmpmH。
2.
For expressing the recombinant GST-FloR1 protein in prokaryote expression system,floR gene was cloned into pGEX-4T-2,and BL21(DE3) codon plus was chose as corresponding expression hosts.
将耐氟苯尼考大肠杆菌的floR基因部分基因片段插入pGEX-4T-2原核表达载体中,构建以BL21(DE3)Codon Plus为宿主菌的原核表达体系。
补充资料：阿斯曼通风干湿表(见通风干湿表)
阿斯曼通风干湿表(见通风干湿表)
AS iman tongfeng ganshibiao阿斯曼通风干湿表见通风干湿表。
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