|Former Common name||No Data|
|H-2 Haplotype||No Data|
|Strain development||Developed by Masaru Okabe, Research Institute for Microbial Diseases, Osaka University. The transgene was injected into the pronuclei of B6C3F1 fertilized eggs. C57BL/6 and C3H mixed background.|
|Strain description||These transgenic mice carry an EGFP (enhanced green fluorescence protein) cDNA under the control of a CAG promoter. Transgene integration site: 15D.|
|Colony maintenance||Carrier x Carrier [or Crossing to Slc:B6C3F1]|
|Health Report||No Data|
|Promoter||CAG promoter (CMV-IE enhancer, chicken beta-actin promoter, rabbit beta-globin genomic DNA)|
|Symbol name||Green Fluorescent Protein (Jellyfish)|
|Common name||No Data|
|Symbol description||No Data|
|References||Genomics. 2002 Dec;80(6):564-74.
FISH analysis of 142 EGFP transgene integration sites into the mouse genome.
|Research applications||Fluorescent Proteins/lacZ System|
|Specific Term and Conditions||The following terms and conditions will be requested by the DEPOSITOR.
The RECIPIENT of BIOLOGICAL RESOURCE shall obtain a prior written consent on use of it 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.
Genomics. 80(6):564-574 (2002).
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. The RECIPIENT which wants to use the BIOLOGICAL RESOURCE even after five years must obtain a written consent from the DEPOSITOR again.
|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.
|Depositor||Okabe, Masaru (Osaka university)|
|Strain Status /