首页> 外文期刊>Experimental Animals >New PCR-RFLP Analysis for the Mouse Tnfsf6~(gld) Gene Caused by a Point Mutation In the Tnfsf6 [Tumor Necrosis Factor (Ligand) Superfamily, Member 6] Locus
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New PCR-RFLP Analysis for the Mouse Tnfsf6~(gld) Gene Caused by a Point Mutation In the Tnfsf6 [Tumor Necrosis Factor (Ligand) Superfamily, Member 6] Locus

机译:Tnfsf6 [肿瘤坏死因子(配体)超家族成员6]基因座突变引起的小鼠Tnfsf6〜(gld)基因的PCR-RFLP新分析

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摘要

A new polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis was developed for genetic typing of the mouse Tnfsf6~(gld) mutation. An artificial restriction site was introduced to the mouse Tnfsf6~(gld) mutation by PCR amplification using a modified primer. The three genotypes of the Tnfsf6 locus (Tnfsf6~(gld)/Tnfsf6~(gld), Tnfsf6~(gld)/+, and +~(Tnfsf6-gld)/+~(Tnfsf6-gld)) could be distinguished clearly and easily. This PCR-RFLP analysis was found to be useful for the identification of the mouse Tnfsf6~(gld) mutation.
机译:建立了一种新的聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析方法,用于小鼠Tnfsf6〜(gld)突变的遗传分型。通过使用修饰引物的PCR扩增,将人工限制性位点引入小鼠Tnfsf6〜(gld)突变。可以清楚地区分Tnfsf6基因座的3个基因型(Tnfsf6〜(gld)/ Tnfsf6〜(gld),Tnfsf6〜(gld)/ +和+〜(Tnfsf6-gld)/ +〜(Tnfsf6-gld))。容易。发现该PCR-RFLP分析对于鉴定小鼠Tnfsf6〜(gld)突变是有用的。

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