Strain Information | |
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Image | |
BRC No. | RBRC02349 |
Type | Targeted Mutation![]() |
Species | Mus musculus |
Strain name | C57BL/6-Fabp7<tm1(cre)Ksak> |
Former Common name | BFABP-Cre |
H-2 Haplotype | |
ES Cell line | RENKA [C57BL/6NCrlCrlj] |
Background strain | C57BL/6NCrlCrlj |
Appearance | |
Strain development | Developed by Mika Tsujita, Rie Natsume and Kenji Sakimura, Brain Research Institute, Niigata University in 2004. RENKA ES cells derived from C57BL/6NCrj were used. C57BL/6N background. |
Strain description | Fabp7 Cre knock-in mice. A Cre sequence was integrated into the start methionine site of the B-FABP gene at an in-frame position. A non-coding and pgk-neo cassette sequence are located downstream from Cre. The pgk-neo cassette can be removed, as it has an frt sequence on both sides. |
Colony maintenance | Heterozygote x Wild-type [C57BL/6NCrlCrlj] |
References |
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 |
Fabp7 MGI:101916 | fatty acid binding protein 7, brain | 10 | Fabp7<tm1(cre)Ksak> | targeted mutation 1, Kenji Sakimura | |||
Frt | yeast FRT (flippase recombination target) site | 10 | Frt | ||||
Frt | yeast FRT (flippase recombination target) site | 10 | Frt | ||||
cre | Phage P1 Cre recombinase | 10 | cre | ||||
neo | neomycin resistance gene (E. coli) | 10 | mouse phosphoglycerate kinase promoter (PGK promoter) | ||||
poly A | mouse pgk polyA | 10 | poly A |
Phenotype | |
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Annotation by Mammalian phenotyhpe ontology | |
Detailed phenotype data |
Ordering Information | |
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Donor DNA | Simian virus 40 Large T antigen nuclear localization signal (NLS), phage P1 Cre, human G-CSF polyadenylation signal sequence (pA), mouse phosphoglycerokinase(pgk) promoter, E. coli neo, mouse pgk poly A, S. cerevisiae 2 micro plasmid FRT sites |
Research application | Cre/loxP system FLP/frt system General Purpose Neurobiology Research |
Specific Term and Conditions | The RECIPIENT of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it from the DEPOSITOR. The RECIPIENT of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it from the DEPOSITOR. The DEPOSITOR should be a co-auther in articles when the users publish their data using these mice for 2 year after provided to the RIKEN BRC. Users should contact the DEPOSITOR in the case of application for any patents with the results from these mice. |
Depositor | Kenji Sakimura (Niigata University) |
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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No Data |