Strain Information | |
|---|---|
| Image | |
| BRC No. | RBRC10323 |
| Type | CRISPR/Cas9 (Transgene) |
| Species | Mus musculus |
| Strain name | B6D2-Ninj2<em1Osb> |
| Former Common name | Ninj2-14/-14 |
| H-2 Haplotype | |
| ES Cell line | |
| Background strain | |
| Appearance | |
| Strain development | Developed by Yoshitaka Fujihara and Masahito Ikawa, Research Institute for Microbial Diseases, Osaka University in 2014. Fertilized eggs derived from BDF1 × BDF1 were used to generate this line. Mixed genetic background. |
| Strain description | Mutant harboring 14 bp deletion at the Ninj2 gene generated by the genome editing technique. Ninj2<em1Osb>; 14 bp deletion at Exon 14.cactatcacctccacatcctcccaacctttcattggtttcaggtcattagctgagcagggaggctgtcactgtcacccaagaggacatttcatcgcctttggggagggtattaaaacccctgtattcttcccagtcccttccagcccttttaccagattctcttctcttatagCACAGGCACTCCATGCGCGGAGGGAACCAGCGCATAGACCTGAACTTTTATGCCACCAAGAAGAGTGTGGCAGAGAGCATGCTAGACGTGGCGCTCTTTATGTCCAATGCCATGCGGCTGAAATCAGTGCTGCAGCAAGGGCCATTCGCGGAGTACTACACCACCCTAGTCACCCTCATCATTGTCTCTCTGCTCCTGCAAGTGGTCATTAGCCTCCTTCTTGTGTTCATCGgtaaggagcccagcctggagtcaggctttctgccttggcgccccctggtggtaggaaaggtccctgcatcatatgtgaaacttcccagccacctgctaacagaggggttacacatctacgcctagg |
| Colony maintenance | |
| References | |
Health Report | |
|---|---|
| Examination Date / Room / Rack | |
Gene | |||||||
|---|---|---|---|---|---|---|---|
| Gene Symbol | Gene Name | Chr. | Allele Symbol | Allele Name | Common Names | Promoter | Diseases Related to This Gene |
| Ninj2 MGI:1352751 | ninjurin 2 | 6 | Ninj2<em1Osb> | endonuclease-mediated mutation 1, Research Institute for Microbial Diseases, Osaka University | |||
Phenotype | |
|---|---|
| Phenotype annotation from literatures by Mammalian phenotype ontology | |
| Detailed phenotype data | |
Ordering Information | |
|---|---|
| Donor DNA | pX330-U6-Chimeric_BB-CBh-hSpCas9[human U6 promoter, S. pyogenes gRNA scaffold, human U6 terminator, CMV,chicken hybrid CMV enhancer/chicken beta-actin promoter (CBh), Synthetic DNA 3xFLAG, SV40 nuclear localization signal(NLS), Streptococcus pyogenes SpCas9 (human codon-optimized), bovine GH polyA signal, AAV2 inverted terminal repeat (ITR), f1 phage f1 origin, E. coli Ampicillin resistance gene (AmpR), E. coli pUC origin], Mouse a part of Ninj2 gene |
| Research application | |
| Specific Term and Conditions | The RECIPIENT of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it as well as consent for collaborative research from the DEPOSITOR. 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 RECIPIENT of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it from the DEPOSITOR. RECIPIENT which wants to use the BIOLOGICAL RESOURCE for the purpose other than education or not-for-profit research is requested to enter into a Material Transfer Agreement with Osaka University. 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. The RECIPIENT which wants to use the BIOLOGICAL RESOURCE even after five years must obtain a written consent from the DEPOSITOR again. |
| Depositor | Masahito Ikawa (Osaka University) |
| Strain Status | Frozen sperm |
| Strain Availability | |
| Additional Info. | Necessary documents for ordering:
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BRC mice in Publications |
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| No Data |