Strain Information | |
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Image | |
BRC No. | RBRC04720 |
Type | Targeted Mutation |
Species | Mus musculus |
Strain name | B6;129S-Rap1a<tm1Morz> Rap1b<tm1Morz> |
Former Common name | B6-Rap1a/Rap1b floxed |
H-2 Haplotype | |
ES Cell line | |
Background strain | |
Appearance | |
Strain development | National Institute of Mental Health・Dr. Alexei Morozov. Developed by Alexei Morozov, National Institute of Mental Health. 129 ES cell derived. The mice were crossed to C57BL/6. |
Strain description | Rap1a and Rap1b floxed mice. Exons 2-3 of Rap1a gene and exon 1 of Rap1b gene were flanked by loxP sites. |
Colony maintenance | Rap1a : Homozygote x Homozygote ; Rap1b : Homozygote x Homozygote [or Crossing to C57BL/6NCrlCrlj] |
References | Enhanced cortico-amygdala efficacy and suppressed fear in absence of Rap1. Pan B X, Vautier F, Ito W, Bolshakov V Y, Morozov A J. Neurosci., 28, 2089-2098 (2008). 18305243 |
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 |
Rap1b | RAS related protein 1b | 10 | Rap1b | targeted mutation 1, Alexei Morozov | |||
Rap1a | RAS-related protein 1a | 3 | Rap1a | targeted mutation 1, Alexei Morozov | |||
loxP | phage P1 loxP | loxP | |||||
loxP | phage P1 loxP | loxP | |||||
neo | neomycin resistance gene (E. coli) | herpes simplex virus thymidine kinase promoter (HSV tk promoter) |
Phenotype | |
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Annotation by Mammalian phenotyhpe ontology | more 1 phenotypes |
Detailed phenotype data |
Ordering Information | |
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Donor DNA | mouse Rapla genomic DNA, mouse Raplb genomic DNA, herpers simplex thymidine kinase promoter, E. coli Neomycin resistance gene, Bacteriophage P1 loxP site |
Research application | Cre/loxP system |
Specific Term and Conditions | a) In all RECIPIENT publications related to the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the following literature designated by the DEPOSITOR is requested: J Neurosci. 2008 Feb 27;28(9):2089-98.Enhanced cortico-amygdala efficacy and suppressed fear in absence of Rap1. Pan BX, Vautier F, Ito W, Bolshakov VY, Morozov A. b) In all publications or presentations of any research results obtained by use of the BIOLOGICAL RESOURCE, RECIPIENT will acknowledge the DEPOSITOR as the source of the BIOLOGICAL RESOURCE. c) Use of the BIOLOGICAL RESOURCE for commercial purposes will require a license agreement between NIH and RECIPIENT. Information can be obtained at https://www.ott.nih.gov./. d) Prior to filing an application for a patent, or intellectual property or other rights based on the use of the BIOLOGICAL RESOURCE, RECIPIENT will first notify the DEPOSITOR. e) RECIPIENT agrees not to claim, infer, or imply endorsement by the DEPOSITOR. f) Unless prohibited by law from doing so, RECIPIENT agrees to hold the DEPOSITOR harmless and to indemnify the DEPOSITOR for all liabilities, demands, damages, expenses and losses arising out of RECIPIENT 's use for any purpose of the BIOLOGICAL RESOURCE. g) This BIOLOGICAL RESOURCE is provided as a service to the research community. IT IS BEING SUPPLIED TO RECIPIENT WITH NO WARRANTIES, EXPRESS OR IMPLIED, INCLUDING ANY WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. RECIPIENT acknowledges that DEPOSITOR makes no representations that the use of the BIOLOGICAL RESOURCE will not infringe any patent or proprietary rights of third parties. |
Depositor | Alexei Morozov (National Institutes of Health) |
Strain Status | Frozen sperm |
Strain Availability | Recovered litters from cryopreserved sperm (2 to 4 months) Cryopreserved sperm (within 1 month) |
Additional Info. | Necessary documents for ordering:
Genotyping protocol -PCR- |
BRC mice in Publications |
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Nagai T, Nakamuta S, Kuroda K, Nakauchi S, Nishioka T, Takano T, Zhang X, Tsuboi D, Funahashi Y, Nakano T, Yoshimoto J, Kobayashi K, Uchigashima M, Watanabe M, Miura M, Nishi A, Kobayashi K, Yamada K, Amano M, Kaibuchi K. Phosphoproteomics of the Dopamine Pathway Enables Discovery of Rap1 Activation as a Reward Signal In Vivo. Neuron 89(3) 550-65(2016) 26804993 |