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1)  toxR gene deficient strains
toxR基因缺失株
1.
Objective To analyze toxR gene function of Vibrio cholerae by construction of toxR gene deficient strains of Vibrio cholerae IEM101 4 and 569B 43.
目的 通过构建霍乱弧菌toxR基因缺失株来研究toxR基因对霍乱弧菌减毒菌株IEM10 1和高产毒株 5 6 9B毒力表达的调控作用。
2)  gene-deleted strain
基因缺失株
1.
Vibrio anguillarum MVAV6203 gene-deleted strain were first incubated in a flask-shaker and 30 liter bioreactor.
应用摇瓶及30 L生物反应器对鳗弧菌MVAV6203基因缺失株进行培养,通过控制流加速率、改变补料方式及补料基质以优化其培养工艺,并用PCR的方法检测培养所得菌体的aroC基因片段。
3)  toxR gene
toxR基因
1.
Molecular cloning and sequence analysis of full-length toxR gene of Vibrio mimicus;
拟态弧菌全长toxR基因的克隆和序列分析
2.
Objective This study was conducted to establish a rapid, simple and accurate method for screening Vibrio parahaemolyticus (VP) by the detection of the specific toxR gene of VP at a species level.
目的以检测toxR基因作为副溶血性弧菌种水平上的特异性基因鉴定,建立一种快速、准确、简便的副溶血性弧菌(VP)筛选方法。
3.
Methods:Primers for specific PCR amplification were designed based on the transmembrane regulatory protein ToxR gene of Vibrio fluvialis.
方法:利用河流弧菌的toxR基因序列设计引物,并对该方法进行特异性、精密度和实际应用等方面的考察。
4)  toxR
toxR基因
1.
Establishment of a Rapid PCR Detection Method for Vibrio fluvialis Based on toxR Gene
基于toxR基因的河流弧菌PCR快速检测方法的建立
2.
A pair of primers were designed accroding to the differential region of toxR genes of vibrio alginolyticus.
为建立溶藻弧菌(Vibrio alginolyticus)的PCR快速检测方法,本研究根据弧菌toxR基因的高变区序列设计1对扩增片段为161 bp的引物,进行了特异性和敏感性试验。
5)  Gene deleted mutant
基因缺失突变株
6)  gene-deleted mutants
基因缺失疫苗株
补充资料:21号染色体部分缺失综合征


21号染色体部分缺失综合征


  病名。即21q-综合征。
  
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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