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1)  Soybean Heat Shock Transcription Factor 8 (Hsf8) Gene
大豆热激转录因子(Hsf8)基因
2)  Heat shock factor 8 gene (hsf8)
热激转录因子8基因
3)  heat shock transcriptional factor
热激转录因子
1.
【Objective】 The rsearch studied the location of the Arabidopsis heat shock transcriptional factor AtHsfA6a in the plant cell and its mechanism.
【目的】研究拟南芥热激转录因子AtHsfA6a在植物细胞中的定位及其作用机制。
2.
A genomic fragment containing the ORF of Arabidopsis heat shock transcriptional factor(AtHsfA6a) was cloned by PCR amplification,and homozygous transgenic Arabidopsis lines containing either over-expression(OE) or antisense(AS) constructs of AtHsfA6a were generated through Agrobacterium-mediated genetic transformation.
从拟南芥基因组中克隆了热激转录因子(At Hsf A6a),构建了过量表达(over-expression,OE)和反义(anti-sense,AS)植物表达载体并转化拟南芥,获得了拟南芥纯合转基因株系。
4)  Heat shock transcription factor
热激转录因子
1.
Plant heat shock transcription factors(HSFs) played the key roles in regulating the expression of heat shock pro-tein genes.
植物热激转录因子主要调控植物热激蛋白基因的转录表达,对植物的耐热性起着重要的作用。
5)  Transcriptional coactivator(TC)
转录辅激活因子(TC)基因
6)  genetically modified soybean
转基因大豆
1.
Using the genetically modified soybean from USA,Argentina,and Brazil as raw materials,we built the Quantitative Detection for CP4 EPSPS protein of glyphosate-resistant,Genetically Modified Soy- bean processed by ELISA method.
以美国、阿根廷、巴西转基因大豆等为材料,建立了ELISA法定量检测抗草甘膦转基因大豆CP4 EP- SPS蛋白的方法,成功检测出美国转基因大豆含量为3。
2.
According to the PCR primers and TaqMan MGB probe of exogenous 35S promotor,the quantitative detection of genetically modified soybean(Roundup ReadyTM) was established by real-time PCR technology.
利用实时荧光定量PCR技术,根据转基因大豆(Roundup ReadyTM)的外源基因35S启动子序列设计引物和TaqMan MGB探针,对大豆粉中Roundup ReadyTM大豆含量进行了定量检测,根据这个检测体系建立了35S启动子Ct值与样品中转基因成分数量之间的标准曲线和线性回归方程(相关系数r2:0。
补充资料:热应激基因
分子式:
CAS号:

性质:一种基因,当短时间地暴露于比生物通常生长温度较高(或较低)的温度之后,这种基因会开始表达或抑制表达。

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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