Information1 | |
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Image | |
BRC No. | RBRC10303 |
Type | Targeted Mutation![]() |
Species | Mus musculus |
Strain name | C3;B6-Lrit1<tm1b(EUCOMM)Hmgu>/Tfur |
Former Common name | Lrit1-gt |
H-2 Haplotype | |
ES Cell line | JM8.N4 [C57BL/6N] |
Background strain | |
Appearance | |
Strain development | Developed by Takahisa Furukawa, Institute for Protein Research, Osaka University in 2017. JM8.N4 ES cells derived from C57BL6/N were used. C3H and B6 mixed genetic background. Mutations of Rd1(Pde6b) and Rd8(Crb1) were replaced with their normal alleles. |
Strain description | Lrit1(leucine-rich repeat, immunoglobulin-like and transmembrane domains 1)mutant mice.A pair of loxP sites flank Exon 2. FRT IRES-LacZ loxP Neo FRT loxP DNA fragment was inserted at intron 1 of the Lrit1 and another loxP was placed at intron 2. Homozygous mutants exhibit abnormality of synapse formation between cone photoreceptor cells and bipolar cells of retina. loxP Neo FRT loxP and Exon 2 DNA fragment was removed by Cre. |
Colony maintenance | |
References | Cell Reports, 22, 3548-3561 (2018). 29590622 |
Health Report | |
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Examination Date / Room / Rack |
Gene | |
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Gene info | Gene symbolGene nameChr.Allele symbolAllele nameCommon namesPromoter Lrit1leucine-rich repeat, immunoglobulin-like and transmembrane domains 114Lrit1<tm1b(EUCOMM)Hmgu>targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH Gene symbolGene nameChr.Allele symbolAllele nameCommon namesPromoter Frtyeast FRT (flippase recombination target) site14Frt Gene symbolGene nameChr.Allele symbolAllele nameCommon namesPromoter loxPphage P1 loxP14loxP |
Information2 | |
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Donor DNA | Yeast FRT site, Mouse En2 intron, encephalomyocarditis virus IRES, E.coli lacZ, SV40 PolyA signal, Bacteriophage P1 loxP site, mouse Lrit1 genomic DNA |
Research application | Cre/loxP system FLP/frt system Fluorescent Proteins/lacZ 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. Cell Reports, 22, 3548-3561 (2018).In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR is requested. RECIPIENT which wants to use the BIOLOGICAL RESOURCE is requested to contact the depositor (Dr. Takahisa Furukawa) and enter into a Material Transfer Agreement with Osaka University. The RECIPIENT shall acknowledge the EUCOMM as the Provider of the ES cells to generate KO mice. |
Depositor | Takahisa Furukawa (Osaka University) |
Strain Status | ![]() |
Strain Availability | Recovered litters from cryopreserved sperm (2 to 4 months) Cryopreserved sperm (within 1 month) |
Additional Info. | Necessary documents for ordering: |
BRC mice in Publications |
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No Data |