1) thrS gene-deficient
thrS基因敲除
2) gene knock-out
基因敲除
1.
Breeding,reproducing and identifying for aquaporin-3 gene knock-out mice;
水通道蛋白3基因敲除小鼠的饲养繁殖及鉴定
2.
Gene knock-out technology and its application in the research of c-Jun NH2-Terminal Kinase-2
基因敲除技术及其在JNK-2研究中的应用
3.
Construction and characterization of a two-component signal transduction system ciaR gene knock-out mutant of Streptococcus suis serotype 2
猪链球菌2型二元信号转导系统ciaR基因敲除突变株的构建及生物学功能研究
3) Gene knockout
基因敲除
1.
Effect of p53 gene knockout on cell migration;
p53基因敲除对细胞迁移的影响
2.
Analysis of focal cerebral blood flow,ATP content and protein sythesis of L1 gene knockout mice;
L1CAM基因敲除小鼠的脑局部血流量、ATP含量和蛋白合成率分析
3.
Establishment of a βB2 crystallin gene knockout mice model;
βB2晶体蛋白基因敲除小鼠模型的建立
4) knockout
[英]['nɔkaʊt] [美]['nɑ'kaut]
基因敲除
1.
Immortalization of embryonic fibroblasts in heat shock transcription factor 1 knockout mouse;
HSF1基因敲除小鼠胚胎成纤维细胞的永生化
2.
Effect of Smad4 Knockout on Hearing and Vestibular Function of Mouse;
Smad4基因敲除对小鼠听力和前庭功能的影响
3.
Experimental observations on the physiology of hearing and cochlea morphology in Smad5 knockout mice;
Smad5基因敲除小鼠听生理和耳蜗形态实验观察
5) knock out
基因敲除
1.
Effects of protein tyrosine phosphatase α knock out on Hippocampal CA1 synaptic plasticity;
PTPα基因敲除对小鼠海马CA1区突触可塑性的影响
2.
Objective To study the role of Schwann cells apoptosis in the pathogenesis of experimental autoimmune neuritis(EAN) in TNF receptor Ⅰ knock out(TNFR Ⅰ-/-)mice.
目的:建立实验性自身免疫性神经炎(EAN)在肿瘤坏死因子α受体I(TNFRⅠ)基因敲除鼠(TNFRⅠ-/-)的动物模型,进一步研究雪旺氏细胞凋亡在其发病机制中的作用。
3.
7kb exon6 to exon7 DNA sequence which is separated by PCR as Short Arm(SA),were used to construct HPRT gene knock out vector.
根据已知大鼠HPRT基因的外显子序列,从大鼠HPRT基因BAC中用酶切和PCR方法分别分离得到用于构建基因敲除载体的3。
6) gene disruption
基因敲除
1.
The gene disruption cassette combined the het- erologous dominant kanr resistance marker with a Cre/loxP-mediated marker removal procedure.
重组质粒pSH-CUP的构建,不仅解决了酵母转化子筛选标记问题和非酵母基因的引入,而且使LoxP-kanMX-loxP基因敲除体系在进行真核生物基因敲除时更加方便可行。
2.
In this thesis,applying the Cre/LoxP system gene disruption method we disrupt the glutamate dehydrogenaseⅠgene(GDH1) from a diploid industry yeast strain SS04 and construct a strain named SS15 of mutating an allele of GDH1, only leaving a single loxP site at the chromosomal locus of GDH1 ORF.
本文以酿酒酵母SS04出发,采用Cre/LoxP系统基因敲除法对酵母谷氨酸脱氢酶Ⅰ基因(GDH1)进行基因敲除操作,构建了一个GDH1等位基因缺失的酿酒酵母菌株SS15,并在原GDH1位置留下了一个LoxP位点。
补充资料：内吸除(见单晶片的吸除技术)
内吸除(见单晶片的吸除技术)
internal gettering
内吸除internal gettering见单晶片的吸除技术。
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