Tfcp2l1tm1.1(cre/ERT2)Ovi
Targeted Allele Detail
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Symbol: |
Tfcp2l1tm1.1(cre/ERT2)Ovi |
Name: |
transcription factor CP2-like 1; targeted mutation 1.1, Catherine E Ovitt |
MGI ID: |
MGI:5662395 |
Synonyms: |
Tcfcp2l1GCE, Tcf-GCE, Tcftm1(GCE)Ovi, Tfcp2l1tm1(cre/ERT2)Ovi |
Gene: |
Tfcp2l1 Location: Chr1:118555675-118612898 bp, + strand Genetic Position: Chr1, 52.14 cM, cytoband E2
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Alliance: |
Tfcp2l1tm1.1(cre/ERT2)Ovi page
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Allele Type: |
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Targeted (Inducible, Recombinase, Reporter) |
Inducer: |
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tamoxifen |
Mutations: |
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Insertion, Intragenic deletion
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Tfcp2l1tm1.1(cre/ERT2)Ovi expression driven by
1 gene
Knock-in expression driven by:
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Mutation details: The targeting construct was generated by inserting the diphtheria toxin A gene (DTA, for positive selection), 3.2 kb 5 homologous arm containing the 5' UTR of exon 1, and 5.5 kb 3 homologous arm containing exon 2 into pBluescript SKII(+). Then the eGFP-CreERT2 (GCE) fragment (McMahon et al. 2008) with an SV40 poly adenylation site and neomycin resistance cassette were inserted immediately downstream of the translational initiation codon ATG. The knock-in construct removed the coding sequences from exon 1 and placed the GCE gene under the control of endogenous regulatory sequences. Flp-mediated recombination removed the selection cassette. The EGFP could not be detected by direct fluorescence or anti-GFP antibody staining.
(J:229520)
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Activity: |
Tissue activity of this recombinase allele
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Driver:
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Tfcp2l1
(mouse)
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Original: |
J:229520 Maruyama EO, et al., Cell-Specific Cre Strains For Genetic Manipulation in Salivary Glands. PLoS One. 2016;11(1):e0146711 |
All: |
2 reference(s) |
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