1) Chinese hamster oocytes cells
中国仓鼠卵母细胞
1.
Effects of eicosatetraynoic acid on hKV1.5 potassium channels transfected in Chinese hamster oocytes cells;
二十碳四烯酸对转基因中国仓鼠卵母细胞hKv1.5钾通道电流的作用
2) Chinese hamster ovary cell
中国仓鼠卵细胞,CHO细胞
3) CHO
中国仓鼠卵巢细胞
1.
EXPRESSION OF HUMAN MUTANT CD59 IN CHO CELL;
人突变CD59在中国仓鼠卵巢细胞中的表达
2.
Objective To study over expression of VMAT_(2) in CHO cells resisted toxicity of MPP~(+) and rotenone.
目的为研究毒物鱼藤酮(rotenone)和1-甲基-4-苯基吡啶离子(MPP+)对野生型及过表达囊泡单胺转运蛋白(VMAT2)的中国仓鼠卵巢细胞(CHO)的毒性作用。
3.
The recombinant vector PCI-neo-PoIFN-γ wased transfer into Chinese hamster ovary cells (CHO) using lipofectamine the strain was screened,and screening training in the presence of G418.
利用脂质体转染法将重组载体PCI-neo-PoIFN-γ转染入中国仓鼠卵巢细胞(CHO)中,在G418的存在下进行筛选培养。
4) Chinese hamster ovary cell
中国仓鼠卵巢细胞
1.
Establishment of stable Chinese hamster ovary cells expressing of high-lever hHGF;
稳定、高效表达肝细胞生长因子的中国仓鼠卵巢细胞系的构建
2.
Functional study of human TSH receptor transfected into Chinese hamster ovary cells;
转染中国仓鼠卵巢细胞人TSH受体的功能评价
3.
Methods The viable region of light chain(VL) and viable region of heavy chain(VH) genes of anti-DR5 antibody were amplified and cloned into the light-and heavy-chain expression vectors respectively,then the recombinant plasmids were co-transfected into dihydrofolate reductase-Chinese hamster ovary cell(CHO-dhfr-) for expression.
方法采用基因工程技术,扩增和克隆抗DR5嵌合抗体的轻、重链表达载体,共转染二氢叶酸还原酶缺陷型中国仓鼠卵巢细胞(CHO-dhfr-),筛选稳定分泌表达抗DR5嵌合抗体的细胞株。
5) Chinese hamster ovary (CHO)
中国仓鼠卵巢(CHO)细胞
6) CHO cell
中国仓鼠卵巢细胞
1.
In order to further study the method for screening GR antagonists, GR cDNA was transiently transfected into CHO cells, and then fluo-3 was loaded into.
1cDNA短暂转染在中国仓鼠卵巢细胞(Chinesehamsterovarycell,CHO)上,加入钙离子敏感性荧光染料(Fluo-3),通过检测荧光强度的改变,筛选GR拮抗剂。
2.
Objective To compare the protective effects of Daidzein and Genistein against H2O2 induced oxidative damage in CHO cell line of healthy subjects and to investigate the antioxidant activity of isoflavones.
目的:研究二羟异黄酮(Daidzein)和三羟异黄酮(Genistein)对H2O2诱导的中国仓鼠卵巢细胞(CHO)氧化损伤的保护作用及探讨其抗氧化活性的作用机制。
3.
The standard and mutated human PrP genes were separately inserted into an eukaryotic expression vector and transfected into CHO cell, respectively, generating CHOs strain containing the standard PrP gene and CHOm strain containing the mutated PrP gene.
将编码朊病毒蛋白的PrP标准及突变DNA序列分别连接到真核表达载体 pcDNA3 1中 ,并分别转入中国仓鼠卵巢细胞 (CHO)。
补充资料：不成熟卵母细胞体外成熟
不成熟卵母细胞体外成熟
是将表皮生长因子和促性腺激素联合用于不成熟卵母细胞进行体外培养，提高受精率及提高不成熟卵母细胞的体外成熟率。它是一项助孕技术，可以减少超排卵带来的经济负担和卵巢过度刺激的危险。解决卵巢本身缺陷诱发排卵无效病人的生育问题，以及为“卵子指赠”工作提供卵母细胞来源，但体外成熟的卵母细胞的胚胎较体内成熟卵母细胞要差，因此必须了解影响卵母细胞体外成熟能力因素和改善培养环境。
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