PCR Method for Genotyping and Zygosity-Testing of RasH2 Transgenic Mice
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- SUEMIZU Hiroshi
- Central Institute for Experimental Animals
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- KITO-MARUYAMA Chika
- Central Institute for Experimental Animals
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- SOTOMARU Yusuke
- Central Institute for Experimental Animals
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- OGURA Tomoyuki
- Central Institute for Experimental Animals
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- HIOKI Kyoji
- Central Institute for Experimental Animals
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- OHNISHI Yasuyuki
- Central Institute for Experimental Animals
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- TAMAOKI Norikazu
- Central Institute for Experimental Animals
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抄録
In short-term carcinogenicity testing using CB6F1-TgrasH2 mice, sibling nonTgrasH2 mice are used as a negative control. However, selection of TgrasH2 and nonTgrasH2 mice has been performed by PCR with only transgene specific primers by the conventional method. Therefore, the conventional method involves the risk of false negative results due to reaction failure, and contamination with TgrasH2 mice in the control mice group. Based on the nucleotide sequence information around the pre-integration site, we developed a genotyping method for distinguishing not only TgrasH2 mice (hemizygous for the Tg allele) but also nonTgrasH2 (homozygous for the nonTg allele) in a positive manner.<br>
収録刊行物
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- Experimental Animals
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Experimental Animals 53 (5), 463-466, 2004
公益社団法人 日本実験動物学会
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詳細情報
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- CRID
- 1390001205041465472
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- NII論文ID
- 10013724101
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- NII書誌ID
- AA11032321
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- ISSN
- 18817122
- 00075124
- 13411357
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- NDL書誌ID
- 7115076
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- PubMed
- 15516796
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可