IFN gamma knockout mice. Homozygous mutant mice show increased susceptibility to infection of intracellular bacteria. D(6か月以上) IFN gamma遺伝子欠損マウス。lacZ遺伝子が挿入されている。細胞内寄生性細菌等に対して易感染性。 D1.129X1-Ifng<tm1Yiw> D1.129X1-Ifng<tm1Yiw> RBRC05126 DBA/1JJmsSlc Yoichiro IWAKURA 1997年 東京大学医科学研究所 岩倉洋一郎先生らにより開発。A3-1 ES細胞由来。DBA/1背景に4世代戻し交配 (BRC寄託時)。129X1/SvJ (A3-1) 1997年 東京大学医科学研究所 岩倉洋一郎先生らにより開発。 A3-1 ES細胞由来。DBA/1背景に4世代戻し交配 (BRC寄託時)。 129X1/SvJ (A3-1) In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the following literature(s) designated by the DEPOSITOR is requested. J Immunol., 159(3):1418-1428 (1997).Please obtain the written consent from Professor Yoichiro Iwakura (iwakura@rs.tus.ac.jp; Research Institute for Biological Sciences, Tokyo University of Science) for the use. 岩倉 洋一郎 Developed by Yoichiro Iwakura, The Institute of Medical Science, The University of Tokyo in 1997. The mice were backcrossed to DBA/1 for at least 4 times. D (more than 6 months) Neomycin resistance gene, lacZ gene (E. coli), PolyA signal (SV40), MC1 promoter (HSV) Necessary documents for ordering:<ol><li>Order form (<A HREF="https://mus.brc.riken.jp/ja/wp-content/uploads/form/form_4.docx">Japanese</A> / <A HREF="https://mus.brc.riken.jp/en/wp-content/uploads/form/form_b.docx">English</A>)</li><li>Category I MTA: MTA for distribution with RIKEN BRC (<A HREF="https://mus.brc.riken.jp/ja/wp-content/uploads/form/form_5.docx">Japanese</A> / <A HREF="https://mus.brc.riken.jp/en/wp-content/uploads/form/form_c.docx">English</A>)</li><li>Acceptance of responsibility for living modified organism (<A HREF="https://mus.brc.riken.jp/ja/wp-content/uploads/form/form_7.docx">Japanese</A> / <A HREF="https://mus.brc.riken.jp/en/wp-content/uploads/form/form_g.docx">English</A>)</li></ol> true 条件を付加する。<br>研究成果の公表にあたって寄託者の指定する文献を引用する。J Immunol., 159(3):1418-1428 (1997).<br>利用者は事前に岩倉洋一郎教授(iwakura@rs.tus.ac.jp;東京理科大学生命医科学研究所)にコンタクトをとり、利用の承諾を得ること。 D1-Ifng KO Immunology and Inflammation Research