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MOUSE LEPTIN RECEPTOR MUTATION GENOTYPE IDENTIFICATION METHOD

机译:小鼠瘦素受体突变基因型鉴定方法

摘要

Quick and effective confirmation of a genotype is important to maintain a mouse model indicating homozygous sterility. A leptin receptor mutation (C57BL/KsJ-db/db) mouse indicating homozygous sterility is generally used as a non-insulin dependent diabetic animal model. Inventors use a tetra-primer ARMS-PCR method for the quick and effective genotype confirmation of a C57BL/KsJ-db/db mouse. 407 bp and 199 bp PCR products are amplified from a normal (+/+) mouse; while 407 bp and 268 bp PCR products are amplified from a homozygous (db/db) mouse; and 497 bp, 268 bp, and 199 bp PCR products are amplified from a heterozygote (db/+) mouse. Furthermore, a tetra-primer ARMS-PCR analysis method is effective for a different mouse having a C57BL/6J gene background. The tetra-primer ARMS-PCR analysis method is effective for system-maintaining C57BL/KsJ-db/db; for mass-producing homozygous (db/db) mice to be used for experiments; and for quickly mass-producing a double knockout mouse containing leptin receptor mutation.;COPYRIGHT KIPO 2016
机译:快速有效地确认基因型对于维持指示纯合不育的小鼠模型很重要。指示纯合不育的瘦蛋白受体突变(C57BL / KsJ-db / db)小鼠通常用作非胰岛素依赖性糖尿病动物模型。发明人使用四引物ARMS-PCR方法来快速有效地确认C57BL / KsJ-db / db小鼠的基因型。从正常(+ / +)小鼠扩增407 bp和199 bp的PCR产物;从纯合(db / db)小鼠中扩增出407 bp和268 bp的PCR产物;从杂合子(db / +)小鼠中扩增出497 bp,268 bp和199 bp的PCR产物。此外,四引物ARMS-PCR分析方法对具有C57BL / 6J基因背景的另一只小鼠有效。四引物ARMS-PCR分析方法对系统维护C57BL / KsJ-db / db有效。用于批量生产的纯合(db / db)小鼠用于实验;并快速大量生产含有瘦蛋白受体突变的双敲除小鼠。; COPYRIGHT KIPO 2016

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