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1)  PGIP
PGIP cDNA
1.
Cloning and sequencing of PGIP cDNA from Prunus mahaleb;
马哈利樱桃PGIP cDNA克隆及序列分析
2)  PGIP gene
PGIP基因
1.
The PGIP gene in Prunus mume Sieb et Zucc.
Longyan)嫩芽中特异性表达的PGIP基因。
2.
A target fragment with a full length of 1 192 bp(Genbank accession:DQ200847) was amplified with genomic DNA of Prunus salicina leaves as the templates and the conservative sequences of PGIP gene as the primers.
以中国李叶片基因组为模板,PGIP基因保守序列为引物,扩增到1条全长1 192 bp的目的片段(Genbank登录号:DQ200847)。
3.
By inserting PGIP in vector P-Super1300+ with super-promoter and nos terminator,a plant super-expressed vector of PGIP gene from Prunus mume was constructed successfully and then transferred to tobacco by Agrobacterium-mediated transformation system.
运用已克隆的梅PGIP基因构建植物超表达载体,将PGIP插入带有启动子super-promoter和终止子nos的中间载体P-Super1300+中,酶切鉴定表明,目的基因已正确地插入载体中。
3)  insoluble PGIP
不溶性PGIP
1.
By using the low - ion buffer and high - ion buffer, the soluble and insoluble PGIP were obtained through ammonium sulfate precipitation, CM - Sepharose FF and Sephadex G - 100 chromatography.
经SDS-PAGE分析:不溶性PGIP出现两条谱带,分子量为41KD和39KD,而可溶性PGIP出现一条谱带,分子量为41KD。
4)  soluble PGIP
可溶性PGIP
1.
By using the low - ion buffer and high - ion buffer, the soluble and insoluble PGIP were obtained through ammonium sulfate precipitation, CM - Sepharose FF and Sephadex G - 100 chromatography.
经SDS-PAGE分析:不溶性PGIP出现两条谱带,分子量为41KD和39KD,而可溶性PGIP出现一条谱带,分子量为41KD。
5)  wheat PGIP
小麦PGIP
1.
Partial structure of wheat PGIP was studied in four aspect: deglycosylation, analysis of partial primary structure, secondary structure and disulfide bond.
本文从去糖基化、部分一级结构分析、二级结构和二硫键分析四个方面对小麦PGIP进行了部分结构的研究,并与双子叶植物PGIP作了比较。
6)  PGIP
PGIP基因
1.
Cloning and Sequence Analysis of PGIP gene and cDNA from Prunus persica
桃PGIP基因及cDNA的克隆及序列分析
2.
Polygalacturonase-inhibiting proteins(PGIPs) belong to a kind of protein family which have the structure of Leucine-rich repeat(LRR) and are primarily localized in the cell wall.
克隆桃PGIP基因并确定其功能是该基因研究利用的基础。
补充资料:J基因
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性质: 为免疫球蛋白V区与C区之间的连接区(J区)编码的基因。

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