首页> 外文期刊>Journal of Camel Practice and Research >ISOLATION, PCR AMPLIFICATION AND CLONING OF HEAT SHOCK PROTEIN GENE FROM SALIVARY GLANDS OF Hyalomma dromedarii TICKS FROM Camelus dromedarius
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ISOLATION, PCR AMPLIFICATION AND CLONING OF HEAT SHOCK PROTEIN GENE FROM SALIVARY GLANDS OF Hyalomma dromedarii TICKS FROM Camelus dromedarius

机译:得自骆驼属骆驼的透明质酸滴虫唾液腺的热休克蛋白基因的分离,PCR扩增和克隆

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摘要

A molecular study was carried out to isolate the heat shock protein gene of Hyalonnna dromedarii ticks of camels, which play important role in their survival under harsh environmental conditions. Engorged adult H. dromedarii ticks were collected from camel herds in the Bikaner district of Rajasthan. Total genomic DNA and RNA was isolated from the salivary glands of ticks. Primers were designed for amplification of heat shock protein gene from H. dromedarii by using base sequence of Haemaphysalis longicornis. The heat shock protein gene of H. dromedarii was successfully amplified from genomic DNA and cDNA and was identified on the basis of its size in agarose gel electrophoresis as 560 bp. The amplicon of expected size was purified from the 1% low melting agarose gel. DNA fragment of interest was then ligated to the pGEM-T Easy vector and ligated mixture was transformed into Escherichia coli JM109 strains for cloning. Screening of recombinants was done by restriction enzyme digestion of plasmid DNA and by colony PCR for quick screening of plasmid insert directly from E. coli colonies in the presence of insert specific primers.
机译:进行了分子研究以分离骆驼的透明质酸tick的热休克蛋白基因,它们在恶劣的环境条件下对其生存具有重要作用。从拉贾斯坦邦比卡内尔地区的骆驼群中收集成年的成年dro虫。从tick的唾液腺中分离出总的基因组DNA和RNA。设计了引物,用于通过使用长血嗜血杆菌的碱基序列从德氏嗜血杆菌中扩增热休克蛋白基因。 dromedarii的热激蛋白基因已成功地从基因组DNA和cDNA中扩增出,并根据其在琼脂糖凝胶电泳中的大小确定为560 bp。从1%低熔点琼脂糖凝胶中纯化出预期大小的扩增子。然后将目的DNA片段连接到pGEM-T Easy载体,并将连接的混合物转化到大肠杆菌JM109菌株中进行克隆。通过限制性内切酶消化质粒DNA并通过菌落PCR筛选重组体,以便在插入特异性引物的存在下直接从大肠杆菌菌落中快速筛选质粒插入物。

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