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B6;129P-Tg(Neurog1-cre/ERT2)1Good/J
Cat. No.: CEMM-07250114
When these Ngn1-CreERT2 transgenic mice are bred with mice containing a loxP-flanked sequence of interest, tamoxifen-inducible, Cre-mediated recombination will result in deletion of the flanked sequences in Neurog1 expressing cells such as neurons in the cortex, hippocampus, thalamus, hypothalamus and the cochlear-vestibular ganglion. This mutant mouse strain may be useful for studying neuron development and lineage mapping of Neurog1 expressing cells.
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Status | Live Mouse Frozen Embryo |
Age | 4 weeks 12 weeks Customized Age |
Sex | Male Female |
GENETICS | |
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Allele Symbol |
Tg(Neurog1-cre/ERT2)1Good
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Allele Name |
transgene insertion 1
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Allele Attributes |
Recombinase-expressing; Inducible
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Gene Symbol |
Tg(Neurog1-cre/ERT2)1Good
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Gene Name |
transgene insertion 1
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Chromosome |
UN
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Expressed Genes |
Cre, Cre recombinase, bacteriophage P1; ESR1, estrogen receptor 1, human
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MGI Accession ID | show more close |
Site of Expression |
Cre is expressed in neurons in the cortex, hippocampus, thalamus, hypothalamus and the cochlear-vestibular ganglion.
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Strain of Origin |
C57BL/6
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Molecular Note |
A transgene was constructed where Cre recombinase fused to the ligand-binding domain of a mutant human estrogen receptor was placed under the control of the upstream promoter and the downstream untranslated region of the Neurog1 gene. Cre activity was detected in cochlear ganglion neurons of transgenic mice when crossed with a Cre-reporter strain and dosing with tamoxifen.
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HUSBANDRY | |
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Suggested Controls |
Noncarrier
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Breeding Considerations |
When maintaining a live colony, these mice can be bred as hemizygotes. The Donating Investigator reports that homozygotes are not viable.
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For Research Use Only.
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