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1)  shRNA-expressing plasmid
shRNA表达质粒
2)  Expression cassettes
shRNA表达框
3)  shRNA expression
shRNA表达
4)  shRNA expression vector
shRNA表达载体
1.
Methods:The shRNA expression vector targeting EGFP gene was constructed, and co-transfected into MCF-7 cells and MCF-7/AdrR cells with pcDNA3.
方法构建针对EGFP基因的shRNA表达载体,与pcDNA3。
2.
Objective To explore the inhibitory effect of shRNA expression vector for mdr1 gene on the expression of P-gp in amycin-resistant human erythroleukemia cell strain K562/ADM.
目的探讨靶向mdr1基因的shRNA表达载体对耐阿霉素的人红白血病细胞(K562/ADM)P-gp表达的抑制作用。
5)  shRNA eukaryotic expressing vector
shRNA真核表达载体
1.
Objective To investigate the effects of human melanin-concentrating hormone receptor 2(MCHR2) specific shRNA eukaryotic expressing vector on binding of radiolabeled ligand to MCHR2.
结论MCHR2基因shRNA真核表达载体能有效减少Bmax、升高Kd值,为利用RNA干扰技术研究人MCHR2基因功能奠定良好的实验基础。
6)  expression vector
表达质粒
1.
PurposeThe expression vector pTYB102 was constructed and active expression of nattokinase gene in E.
目的构建大肠杆菌表达质粒pTYB10 2 ,实现纳豆激酶基因 (nattokinasegene)在大肠杆菌中高活性表达。
2.
Recombinant expression vector was constructed and sequenced after enzyme digestion.
方法 :采用RT -PCR技术 ,从正常人外周血单个核细胞中扩增编码CD1 5 8b的cDNA ,经酶切后将其克隆于pMBP -c表达质粒上 ,酶切和测序鉴定。
3.
The full-length cDNA fragment encoding human C1-INH was obtained by gene recombination techniques and a stable expression plasmid was constructed by inserting the human C1-INH cDNA into an efficient dicistronic expression vector pED.
利用基因工程手段获取编码人补体1抑制物(C1-inhibitor,C1-INH)的基因片段,将其插入双顺反子表达载体pED中,构建成功可在CHO细胞中有效表达人C1-INH的表达质粒。
补充资料:[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]
分子式:C16H16ClN3O3S
分子量:365.5
CAS号:26807-65-8

性质:暂无

制备方法:暂无

用途:用于轻、中度原发性高血压。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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