CPXCR1
CPX chromosome region, candidate 1
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CT77
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- Human(53336) Summary: This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc-finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]
- Mouse(382239) CPX chromosome region, candidate 1
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Antibodies
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Anti-CPXCR1 antibody produced in mouse, purified immunoglobulin, buffered aqueous solution,
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human
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immunofluorescence
western blot
western blot
Anti-CPXCR1 antibody produced in rabbit, IgG fraction of antiserum,
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human
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western blot
esiRNA
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