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首页> 外文期刊>The Veterinary Journal >Two novel real-time PCR methods for genotyping the von Willebrand disease type I mutation in Doberman Pinscher dogs.
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Two novel real-time PCR methods for genotyping the von Willebrand disease type I mutation in Doberman Pinscher dogs.

机译:两种新颖的实时PCR方法用于对杜宾犬的von Willebrand疾病I型突变进行基因分型。

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摘要

Two single tube real-time PCR methods were designed to genotype the mutation responsible for von Willebrand disease type I (von Willebrand factor c.7437G > A) in Doberman Pinscher dogs: (1) the Divergent PCR assay, which is a modification of the bi-directional PCR amplification of a specific allele (BI-PASA) technique, and (2) a minor groove binder (MGB) real-time PCR assay using fluorescently labelled probes. There was complete agreement between the genotypes determined using the two real-time PCR methods and the results of sequencing of PCR products generated by conventional PCR from genomic DNA purified from the blood of 27 Doberman Pinscher dogs. The Divergent PCR assay yielded reliable results with >=6.4 ng genomic DNA per reaction and the MGB real-time PCR assay yielded reliable results with >=150 pg genomic DNA per reaction. Both real-time PCR methods are suitable for routine genetic testing for the von Willebrand disease type I mutation using blood samples.
机译:设计了两种单管实时PCR方法对杜宾犬的I型von Willebrand疾病(von Willebrand因子c.7437G> A)负责的突变进行基因分型:(1)Divergent PCR分析,这是对特定等位基因(BI-PASA)技术的双向PCR扩增,以及(2)使用荧光标记探针的小沟结合物(MGB)实时PCR测定。使用两种实时PCR方法确定的基因型与通过常规PCR从27只杜宾犬血液中纯化的基因组DNA生成的PCR产物的测序结果完全一致。 Divergent PCR分析产生可靠的结果,每个反应的> = 6.4 ng基因组DNA,MGB实时PCR分析产生可靠的结果,每个反应的 150 pg基因组DNA。两种实时PCR方法均适用于使用血样对von Willebrand疾病I型突变进行常规基因检测。

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