Rat Synapsin1 promoter, phage P1 Cre recombinase, human Estrogen receptor binding domain (ERT2) cDNA, SV40 poly A signal 条件を付加する。<br>研究成果の公表にあたって謝辞の表明を必要とする。<br>利用者は、事前に寄託者の提供承諾（大阪大学とのMTA締結）を得る。 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> B6.Cg-Tg(Syn1-creERT2)1Tfur B6.Cg-Tg(Syn1-creERT2)1Tfur Carrier x Noncarrier [C57BL/6] These transgenic mice express the cre ERT2 under the control of the rat 4.3 kb synapsin 1 promoter. Carrier x Noncarrier [C57BL/6] B（1〜3か月） ラット由来Synapsin-1 4.3 kbプロモーター制御下でcreERT2を発現するトランスジェニックマウス。タモキシフェンによりCreを誘導可能。, true Developed by Yoshihiro Omori and Takahisa Furukawa, Institute for Protein Research, Osaka University in 2012. The transgene was injected into the pronuclei of B6C3F1 fertilized eggs. The mutant mice were crossed to C57BL/6. In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR is requested. Prior to requesting the BIOLOGICAL RESOURCE, the RECIPIENT must contract an MTA with the DEPOSITOR (Osaka University). 古川　貴久 ラット由来Synapsin-1 4.3 kbプロモーター制御下でcreERT2を発現するトランスジェニックマウス。タモキシフェンによりCreを誘導可能。 Syn1-CreERT2 Tg, B6-Syn1-CreER Tg Syn1-CreERT2 Tg, B6-Syn1-CreER Tg Furukawa Takahisa <a href='https://brc.riken.jp/mus/pcr06220'>Genotyping protocol -PCR-</a> Cre/loxP system B (1-3 months) RBRC06220 大阪大学蛋白質研究所・大森義裕先生、古川貴久先生（2012）。B6C3F1受精卵を用いて作出。