B6J.129-Pex5tm1Pec/BaesJ

Cat. No.: CEMM-07250884

Common Name: B6J.Pex52loxP; B6J.Pex5-loxP; B6J.Pex5FL
Pex52loxP (Pex5-loxP, Pex5FL) mice have loxP sites flanking exons 11-14 (the four exons encoding several tetratricopeptide repeat domains that are essential for PEX5 function). See the Detailed Description section for additional information regarding the number of loxP sites. Deletion of the floxed sequences creates a null allele. These Pex52loxP mice are useful for studying the absence of functional peroxisomes in selective organs and at different stages of life, and are a model for studying characteristics of Zellweger Spectrum Disorder (ZSD).Pex52loxP mice are available on a C57BL/6J genetic background (B6J.Pex52loxP;) and on a Swiss outbred background (SWISS.Pex52loxP;).
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Status Live Mouse
Frozen Embryo
Age 4 weeks
12 weeks
Customized Age
Sex Male
Female
GENETICS
Allele Symbol
Pex5tm1Pec
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Allele Name
targeted mutation 1
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Allele Attributes
Conditional ready (e.g. floxed); No functional change
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Gene Symbol
Pex5
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Gene Name
peroxisomal biogenesis factor 5
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Chromosome
6
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Strain of Origin
(129X1/SvJ x 129S1/Sv)F1-Kitl+
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Molecular Note
Four exons encompassing sequence encoding several tetratricopeptide repeat domains were flanked by an upstream floxed neo cassette and a downstream intronic loxP site. Transient transfection of ES cells with plasmids expressing Cre resulted in the excision of the floxed neo cassette, leaving single loxP sites in the introns surrounding the four exons.
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HUSBANDRY
Suggested Controls
C57BL/6J
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Breeding Considerations
Mice heterozygous or homozygous for this floxed allele are viable and fertile with normal fertility and peroxisomal metabolism, and no gross phenotypic or behavioral abnormalities. When maintaining a live colony, heterozygous mice may be bred together, to wildtype mice from the colony or to C57BL/6J inbred mice. Alternatively, homozygous mice may be bred together.
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Breeding Strategy
Homozygote x Homozygote
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For Research Use Only.
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