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B6.129P2-Mecp2tm2Bird/J
Cat. No.: CEMM-07250060
Common Name: Mecp2lox-STOP
Mice with this X-linked lox-STOP mutation of the methyl CpG binding protein 2 gene may be useful in neurological and developmental studies of Rett syndrome and its amelioration upon excision of the lox-STOP cassette.
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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 |
Mecp2tm2Bird
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Allele Name |
targeted mutation 2
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Allele Attributes |
Conditional ready (e.g. floxed); Null/Knockout
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Gene Symbol |
Mecp2
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Gene Name |
methyl CpG binding protein 2
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Chromosome |
X
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MGI Accession ID | show more close |
Strain of Origin |
129P2/OlaHsd
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Molecular Note |
Cre recombinase-reversible gene inactivation was accomplished by insertion into intron 2 of a 3.1-kb DNA fragment containing a loxP-flanked "neostop" cassette, which comprises a neomycin resistance cassette followed by a transcriptional/translational "stop" cassette composed of 550 bp of 3' sequence from the Saccharomyces cerevisiae His3 gene, an SV40 polyadenylation sequence, and a synthetic sequence containing a false translation initiation codon (ATG) immediately followed by a consensus splice donor sequence. Despite the production of a read-through transcript, no protein product was detected by western blot or immunofluorescence analysis of brains of mutant mice.
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HUSBANDRY | |
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Suggested Controls |
C57BL/6J Wild-type from the colony
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Breeding Considerations |
When maintaining a live colony, females heterozygous for this X-linked mutation can be bred with wildtype male siblings. The donating investigator recommends replacing heterozygous female breeders when Rett syndrome symptoms appear or when females fail to produce or care for regular litters (may be as early as 4-6 months). The donating investigator also reports that breeding performance may be improved if mice are maintained on a mixed C57BL/6;BALB/c background.
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For Research Use Only.
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