Strain Information | |
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Image | |
BRC No. | RBRC03934 |
Type | Transgene![]() |
Species | Mus musculus |
Strain name | C57BL/6N-Tg(Ins1-cre)25Utr/Rbrc |
Former Common name | Insulin-NLSCre |
H-2 Haplotype | |
ES Cell line | |
Background strain | C57BL/6NCrlCrlj |
Appearance | |
Strain development | Developed by Laboratory Animal Resource Center, University of Tsukuba and RIKEN BioResrouce Center in 2009. The transgene was injected into the pronuclei of C57BL/6N fertilized eggs. |
Strain description | BAC Ins1-Cre transgenic mice. The mice were generated by using a BAC clone containing the mouse Ins1 gene, PR23-181I21. The Cre gene was inserted by homologous recombination into the second exon with a translational initiation codon in the Ins1 BAC clone. 6 founder lines were generated. The R26R crossing test indicated that line 25 (RBRC03934) is useful cre-driver for pancreatic beta cell-specific Cre-loxP recombination. |
Colony maintenance | Carrier x Noncarrier [C57BL/6NCrlCrlj]. Hemizygous Tg mice are viable and fertile (viability and fertility of homozygotes are unknown). |
References | Novel ROSA26 Cre-reporter knock-in C57BL/6N mice exhibiting green emission before and red emission after Cre-mediated recombination. Hasegawa Y, Daitoku Y, Sekiguchi K, Tanimoto Y, Mizuno-Iijima S, Mizuno S, Kajiwara N, Ema M, Miwa Y, Mekada K, Yoshiki A, Takahashi S, Sugiyama F, Yagami K Exp. Anim., 62, 295-304 (2013). 24172193Generation and characterization of Ins1-cre-driver C57BL/6N for exclusive pancreatic beta cell-specific Cre-loxP recombination. Hasegawa Y, Daitoku Y, Mizuno S, Tanimoto Y, Mizuno-Iijima S, Matsuo M, Kajiwara N, Ema M, Oishi H, Miwa Y, Mekada K, Yoshiki A, Takahashi S, Sugiyama F, Yagami K Exp. Anim., 63(2):183-191 (2014). 24770644 |
Health Report | |
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Examination Date / Room / Rack |
Gene | |||||||
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Gene Symbol | Gene Name | Chr. | Allele Symbol | Allele Name | Common Names | Promoter | Diseases Related to This Gene |
Frt | yeast FRT (flippase recombination target) site | UN | Frt | ||||
cre | Phage P1 Cre recombinase | UN | cre | ||||
loxP | phage P1 loxP | UN | loxP | ||||
nls | SV40 large T antigen nuclear localization signal (NLS) | UN | nls | mouse Insulin promoter (beta cell specific promoter region) | |||
SV40 polyA | UN |
Phenotype | |
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Annotation by Mammalian phenotyhpe ontology | |
Detailed phenotype data |
Ordering Information | |
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Donor DNA | Phage P1 cre recombinase, yeast FRT (flippase recombination target) site, mouse Insulin promoter (beta cell specific promoter region), SV40 polyA, SV40 nuclear location signal(nls), Phage P1 loxP site derived from pBACe3.6 vector, BAC clone RP23-181I21 |
Research application | Cre/loxP system FLP/frt system |
Specific Term and Conditions | 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. Exp. Anim., 63(2):183-191 (2014). In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to Dr. Ken-ichi Yagami, Laboratory Animal Resource Center, University of Tsukuba and RIKEN BioResource Center is requested. 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. (will be announced) The availability of the BIOLOGICAL RESOURCE is limited to a RECIPIENT of a not-for profit institution for a not-for-profit research. For use of the BIOLOGICAL RESOURCE by a for-profit institution, the RECIPIENT must reach agreement on terms and conditions of use of it with DEPOSITOR and must obtain a prior written consent from the DEPOSITOR. RECIPIENT must contact the DEPOSITOR in the case of application for any patents or commercial use based on the results from the use of the BIOLOGICAL RESOURCE. |
Depositor | RIKEN BRC (RIKEN BRC) |
Strain Status | ![]() ![]() |
Strain Availability | Recovered litters from cryopreserved embryos (2 to 4 months) Cryopreserved sperm (within 1 month) Cryopreserved embryos (within 1 month) |
Additional Info. | Necessary documents for ordering:
Genotyping protocol -PCR- |
BRC mice in Publications |
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Ueki K, Nishida Y, Aoyama S, Uzawa H, Kanai A, Ito M, Ikeda K, Iida H, Miyatsuka T, Watada H. Establishment of Pancreatic Beta Cell-specific Gene Knockout System Based on CRISPR-Cas9 Technology with AAV8-mediated gRNA Delivery. Diabetes (2023) 37625131 |