|Former Common name||B6-ROSA26/CAG-GFP|
|H-2 Haplotype||No Data|
|ES cell line||E14TG2a [129P2/OlaHsd]carries Hprt
|Background strain||No Data|
|Strain development||Develop by Masato Ohtsuka, Tokai University School of Medicine in 2010. The mice were backcrossed to C57BL/6JJcl. Extra sequence in the RMCE<ex> was removed by FLPe injection.|
|Strain description||The mice having a CAG-EGFP-polyA cassette at the ROSA26 locus that were generated by RMCE (Recombinase-mediated cassette exchange). The mutant mice exhibit ubiquitous and very bright fluorescence.|
|Colony maintenance||Homozygote x Homozygote [or Crossing to C57BL/6JJcl]|
|Symbol name||gene trap ROSA 26, Philippe Soriano|
|Common name||No Data|
|Symbol description||No Data|
|References||Nucleic Acids Res. 2010 Dec 1;38(22):e198. Epub 2010 Sep 29.
Pronuclear injection-based mouse targeted transgenesis for reproducible and highly efficient transgene expression.
|Research applications||Cre/loxP system,
Fluorescent Proteins/lacZ System
|Specific Term and Conditions||The following terms and conditions will be requested by 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. Nucleic Acids Res., 38, e198 (2010). For use of the BIOLOGICAL RESOURCE by a for-profit institution, the RECIPIENT must reach agreement on terms and conditions of use of it with DEPOSITOR and must obtain a prior written consent from the DEPOSITOR. RECIPIENT must contact the DEPOSITOR in the case of application for any patents or commercial use based on the results from the use of the BIOLOGICAL RESOURCE.
|1||GFP Transfer License (Japanese / English)
Please fill in the Schedule A, and submit two signed copies to us together with two signed copies of RIKEN BRC’s MTA. Please also read Schedule B.
|2||Genotyping protocol <PCR>|
|Depositor||Ohtsuka, Masato (Tokai University)|
|Strain Status /