Japanese
NBRP Rat No: 0637
Strain Name
:
F344.W-Tg(Nanog-GFP,-PuroR)Kyo
Commmon Name: nanog-GFP reporter rat
Principal Investigator
Birger Voigt
Organization
Graduate School of Medicine, Kyoto University Institute of Laboratory Animals
Address
Yoshidakonoe-cho, Sakyo-ku
606-8501 Kyoto
JAPAN
Telephone
075-753-9318
Fax: 075-753-4409
birger@anim.med.kyoto-u.ac.jp
Inbred Generations
N7 (April 2012)
Coat Color
Deposition Status
albino (A,B,c,h)
Embryo
Sperm
Live Animals
Usage Restrictions
The recipient of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it from the DEPOSITOR.
In publishing, a citation of the following literature(s) designated by the DEPOSITOR is requested. (see references)
For a commercial use of this resource, a new contract must be concluded between the depositor and the RECIPIENT.
The RECIPIENT recognizes and acknowledges that the BIOLOGICAL RESOURCE was created by the scientist at KYOTO UNIVERSITY from Nanog-IRES-Puro mouse by utilizing the Red/ET Recombineering technology of Gene Bridges GmBH.
Genetic Status
Inbred
Segregating
Congenic
Consomic
Recombinant
Coisogenic
Spont. Mutant
Transgene
Ind. Mutant
Others
Comercial Availability
Research Category
Diabetes Obesity
Neurobiology
Ophthalmology
Dentistry
Cardio- Hypertension
Oncology
Metabolism
Otorhinology
Immunology
Infectious Disease
Osteology
Internal Medicine
Dermatology
Reproduction
Development
Behavior
Hematology
Urology
Pharmacology
Others stem cell research
Control Strains
Reporter gene Strains
Gene
Nanog
Origin
W-Tg(Nanog-GFP,-puro-r)/22Kyo rats were backcrossed to F344/Stm to transfer the transgene onto a different genetic background
Strain Characteristics
Nanog-GFP IRES puro-resistance transgene was generated by insertion of GFP-IRES-puromycin resistance gene (Puror) cassette into the 5' untranslated region of a bacterial artificial chromosome (BAC) containing the mouse Nanog gene. ES and iPS cells with the Nanog-GFP transgene are positive for GFP.
Breeding Conditions
normal breeding performance
Genotyping
mouse nanog-GFP BAC can be detected using the following primer pair:
PHF5’BamH1 TGGGATCCCTATGCTACTCCGTCGAAGTTC
6047AS10 CTAGGCAAACTGTGGGGACCAGGAAGAC
Annealing 63°C; 30 cycles standard PCR conditions
References
Okita, K. et al., Generation of germline-competent induced pluripotent stem cells. Nature 448: 313-317(2007)