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>
関口 清俊
Kiyotoshi SEKIGUCHI
Bacteriophage P1 loxP sequence
RBRC05656
Qbrick (Frem1) RGD (rg-Gly-Asp) knock-in mice. Exon 4 of Frem1 containing the codon encoding Asp207 was replaced with a mutated exon in which the codon encoding Asp207 was substituted with a codon encoding Glu207.
C (3-6 months)
条件を付加する。<br>利用者は研究成果の公表にあたって謝辞の表明を必要とする。
Qbrick<RGE>, B6-Frem1/RGE KI
Qbrick<RGE>, B6-Frem1/RGE KI
Cre/loxP system
Qbrick (Frem1) ゲノム上のArg-Gly-Asp (RGD) 配列をコードする部分がArg-Gly-Glu (RGE) となるよう変異を挿入したマウス。Qbrickは基底膜分子であり、インテグリン結合モチーフであるArg-Gly-Asp (RGD) 配列を有する。RGE変異配列にはインテグリン結合活性はない。
大阪大学蛋白質研究所・関口清俊(2012)。129系統由来ES細胞を用いて作製。C57BL/6Jマウスと交配された。
In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR is requested.
C(3〜6か月)
B6;129-Frem1<tm2.1Ksek>
B6;129-Frem1<tm2.1Ksek>
Cell Biology Research
Developed by Kiyotoshi Sekiguchi, Institute for Protein Research, Osaka University in 2012. 129 derived ES cells were used. The mutant mice were crossed to C57BL/6J. A floxed neo cassette was removed by cre-mediated recombination.
Heterozygote x Wild-type [C57BL/6JJmsSlc]
Heterozygote x Wild-type [C57BL/6JJmsSlc]
true