| Image |
|
||||||
| Caption | (A) The Cdk1 genomic locus (I) was modified in ES cells with the targeting vector (II) shown. An FRT-flanked neomycin-selection cassette was introduced along with LoxP recombination sites (red triangles) on both sides of exon 3, which generated a mutant Cdk1 locus (III). For Southern blot analysis, 5' and 3' probes located outside the targeting vector were used, after an EcoRV (RV) digest, resulting in a 31,206-bp (recombinant) and a 9,110-bp (5') or 20,300-bp (3') fragment for wild-type. Upon expression of FLP recombinase, the neomycin cassette was removed, and only the LoxP sites remained in the locus (IV, Cdk1FLOX), generating the Cdk1tm2.1Kald allele. After Cre recombinase expression, exon 3 was excised (V), which resulted in deletion of Cdk1 and a frame shift, generating the Cdk1tm2.2Kald allele. PCR genotyping primers are indicated (Pr1, -2, and -3). To generate Cdk1 knockouts, floxed mice were crossed with beta-actin-Cre mice, expressing Cre recombinase ubiquitously in all tissues, including germ line. | ||||||
| Copyright | This image is from Diril MK, Proc Natl Acad Sci U S A 2012 Mar 6;109(10):3826-31. Copyright 2012 National Academy of Sciences, U.S.A. J:182141 | ||||||
|
Associated Alleles |
|
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 11/12/2024 MGI 6.24 |
|
|
|
||
Analysis Tools