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B6.Cg-Gnb4tm1.1(cre/ERT2)Hze/J
Cat. No.: CEMM-07250779
Common Name: Gnb4-IRES2-CreERT2-D knock-in
Gnb4-IRES2-CreERT2-D knock-in mice express tamoxifen-inducible Cre recombinase from the endogenous guanine nucleotide binding protein (G protein) beta 4 promoter/enhancer elements. When induced, CreERT2 expression/activity is enriched in restricted populations within cortical subplate (claustrum and endopiriform nucleus) and layers 5/6 of lateral areas of cortex. Expression is also observed in some vascular cells. These mice may be used to generate conditional mutations for studying gain-or-loss of function and/or fate mapping related to this G protein.
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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 |
Gnb4tm1.1(cre/ERT2)Hze
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Allele Name |
targeted mutation 1.1
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Allele Attributes |
Recombinase-expressing; Inducible
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Gene Symbol |
Gnb4
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Gene Name |
guanine nucleotide binding protein (G protein)
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Chromosome |
3
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Expressed Genes |
cre/ERT2, Cre recombinase and estrogen receptor 1 (human) fusion gene
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MGI Accession ID | show more close |
Site of Expression |
CreERT2 is inducible following Tamoxifen administration, and When bred with mice containing lox-flanked sequences, Tamoxifen-inducible Cre-mediated recombination will result in deletion of floxed sequences in Gnb4-expressing cells of the offspring such as in the cortex and some vascular cells.
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Strain of Origin |
(129S6/SvEvTac x C57BL/6NCrl)F1
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Molecular Note |
The targeting vector contained, from 5' to 3', a partial Gnb4 sequence spanning intron 6 through intron 9 and part of exon 10 (including the endogenous stop codon), an internal ribosome entry site 2 (IRES2) sequence (allows translation initiation in the middle of an mRNA sequence), a CreERT2 fusion gene (Cre-ERT2; Cre recombinase fused to a G400V/M543A/L544A triple mutation of the human estrogen receptor ligand binding domain), a bovine growth hormone polyA sequence, an AttB site, a PGK promoter-Neomycin resistance gene-PGK polyA cassette, an frt5 site, an mRNA splice acceptor sequence, the 3' portion of the hygromycin gene (Hygro2) with SV40 polyA signal, and an AttP site. This targeting vector was electroporated into G4 ES cells. Correctly targeted ES cells were injected into recipient blastocysts. The resulting chimeric animals were bred to PhiC31-expressing mice to delete the AttB/AttP-flanked sequences and replace it with the recombined AttB/AttP site (AttL). The tamoxifen-inducible Cre recombinase activity is enriched in restricted populations within cortical subplate (claustrum and endopiriform nucleus) and layers 5/6 of lateral areas of cortex. Expression is also observed in some vascular cells.
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HUSBANDRY | |
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Suggested Controls |
C57BL/6J
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Breeding Considerations |
When maintaining a live colony, heterozygous mice may be bred together, to wildtype mice from the colony or to C57BL/6J inbred mice. it has not been attempted to make this strain homozygous.
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Breeding Strategy |
Wild-type x Heterozygote; Heterozygote x Wild-type
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For Research Use Only.
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