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B6.Cg-Gnb4tm1.1(cre)Hze/J
Cat. No.: CEMM-07250738
Common Name: Gnb4-IRES2-Cre-D knock-in
Gnb4-IRES2-Cre-D knock-in mice are designed to have Cre recombinase expression directed to guanine nucleotide binding protein (G protein) beta 4-expressing cells. Cre recombinase expression and activity largely recapitulates the endogenous Gnb4 gene - it is enriched in claustrum but relatively sparse in nearby structures (endopiriform nucleus and deep insular cortex). 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.
Inquiry
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)Hze
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Allele Name |
targeted mutation 1.1
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Allele Attributes |
Recombinase-expressing
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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, Cre recombinase, bacteriophage P1
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MGI Accession ID | show more close |
Site of Expression |
Cre recombinase expression and activity largely recapitulates the endogenous Gnb4 gene - it is enriched in claustrum but relatively sparse in nearby structures (endopiriform nucleus and deep insular cortex).
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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, an frt3 site within Gnb4 intron 9, a partial Gnb4 exon 10 sequence up to and including the endogenous stop codon, an internal ribosome entry site 2 (IRES2) sequence (allows translation initiation in the middle of an mRNA sequence), a Cre recombinase gene, 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 construct was electroporated into (129S6/SvEvTac x C57BL/6)F1-derived G4 embryonic stem (ES) cells. Correctly targeted ES cells were injected into recipient blastocysts. Chimeric mice were bred to PhiC31-expressing mice to remove the the AttB/AttP-flanked PGK-neo sequence and replace it with the recombined AttB/AttP site (AttL).
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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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