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
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
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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