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通过限制性片段长度多态性(RFLP)和异源双链分析追踪转基因小鼠中的H-2等位基因。

Tracking H-2 alleles in transgenic mice by RFLP and heteroduplex analysis.

作者信息

Shanmugam V, Haines D, Lake J P, Saha B K

机构信息

Department of Pathology, Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

Transgenic Res. 1996 May;5(3):203-8. doi: 10.1007/BF01969710.

Abstract

Transgenic mice provide valuable tools for biological research including many areas of immunology. In studies involving the major histocompatibility complex (MHC), it is often necessary to place the desired transgene in a specific H-2 (the murine MHC) environment. In this regard, the strains commonly used for the production of transgenic mice also carry well characterized H-2 alleles and provide an appropriate genetic background for MHC related experiments. In this study, a highly polymorphic microsatellite of tetranucleotide repeats from the second intron of the class II Eb gene within the H-2 complex was used in order to identify the corresponding alleles. The relevant H-2 allele(s) along with the transgene were then tracked throughout the production of a chicken ovalbumin-specific transgenic strain. The technique involved PCR-amplification of a DNA sequence encompassing the H-2 specific microsatellite followed by RFLP and heteroduplex analyses. This approach is likely to find wide application in the background checking of transgenic mice, especially in immunological research requiring a defined H-2 background.

摘要

转基因小鼠为包括许多免疫学领域在内的生物学研究提供了有价值的工具。在涉及主要组织相容性复合体(MHC)的研究中,常常需要将所需的转基因置于特定的H-2(小鼠MHC)环境中。在这方面,常用于生产转基因小鼠的品系也携带特征明确的H-2等位基因,并为与MHC相关的实验提供了合适的遗传背景。在本研究中,使用了H-2复合体中II类Eb基因第二个内含子的一个高度多态的四核苷酸重复微卫星来鉴定相应的等位基因。然后,在生产鸡卵清蛋白特异性转基因品系的整个过程中追踪相关的H-2等位基因和转基因。该技术包括对包含H-2特异性微卫星的DNA序列进行PCR扩增,随后进行RFLP和异源双链分析。这种方法很可能在转基因小鼠的背景检测中得到广泛应用,尤其是在需要明确H-2背景的免疫学研究中。

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