| NBRP Rat No: 0937 |
Strain name: WIC-Myod1em2Kykn |
Commmon Name: MyoD-deficient (+1 bp) |
Rat Genome Database |
| Principal Investigator: |
Keitaro Yamanouchi The University of Tokyo 1-1-1, Yayoi, Bunkyo-ku, 113-8657 Tokyo Japan |
| Tel: 03-5841-5386 Fax: 03-5841-8017 |
Email: akeita@g.ecc.u-tokyo.ac.jp |
| Preservation Status: |
Embryo Sperm Living Animals |
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| Coat Color |
白色 |
| Inbred Generations |
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| Usage Restrictions |
In publishing the research results to be obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR is requested. |
| Genetic Status |
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| Comercial Availability |
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| Research Category |
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| Gene Affected |
MyoD |
| Origin |
A mutation was introduced into the MyoD gene of Wistar-Imamichi rats (Iar: Wistar-Imamichi, Institute for Animal Reproduction) using the CRISPR/Cas9 method. A single base was inserted into Exon1.
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| Strain characteristics |
MyoD-deficient rats (-/-) die neonatally within 24 hours after birth.
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| Breeding Conditions |
Maintained by natural mating between heterozygous rats.
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| Genotyping |
The genotype of each rat is examined by PCR.
Primer F: ATTGTACTATTGGGGTTCAGGAGTG
Primer R: CAGACCTTCAATGTAGCGGATG
PCR conditions: KOD FX Neo is used.
94℃ 5 min x 1 cycle 98℃ 10 sec, 58℃ 30 sec, 68℃ 40 sec x 38 cycles.
After PCR, the product is treated with the restriction enzyme Bsl1. A microchip electrophoresis device for DNA/RNA analysis (Multina) is used for analysis.
Wild type: 154 bp, homozygous deletion: 123 bp, heterozygous: 154 bp and 123 bp digestion products are detected.
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| References |
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| Additional strain information |
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