| Primary Identifier | MGI:5303441 | Allele Type | Targeted |
| Attribute String | Reporter | Gene | Hprt1 |
| Transmission | Cell Line | Strain of Origin | (B6.129P2-Hprt1<b-m3>/J x 129S-Gt(ROSA)26Sor<tm1Sor>/J)F1 |
| Is Recombinase | false | Is Wild Type | false |
| Project Collection | Pleiades Promoter Project |
| molecularNote | The Ple12-EGFP plasmid (pEMS1241) was created by inserting the Ple12 MiniPromoter (derived from specific promoter/enhancer/regulatory regions of the human arginine vasopressin (AVP) gene) into the multiple cloning site of the pEMS1307 plasmid vector backbone. This placed the Ple12 MiniPromoter upstream of a full F5 mutant-frt site, a Kozak consensus sequence, an enhanced green fluorescent protein (EGFP; with mutated TAA to TTA stop), a tetracysteine residue, a nuclear localization signal, a full wildtype frt site, an SV40 early mRNA polyA signal, a human HPRT complementary sequence (containing exon 1, intron 1, exon 2, and part of intron 2), a mouse 3' Hprt homology arm, an I-Sce linearization cut site, and a mouse 5' Hprt homology arm. This Ple12-EGFP construct was targeted as a single copy knock-in to the Hprtb-m3 mutant locus on the X Chromosome via electroporation into mEMS1204 embryonic stem cells. |
