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Merck

CPXCR1

CPX chromosome region, candidate 1

Synonymes:
CT77
Espèce(s):
ID UniProtKB:
ID du gène:
  • 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

Référence du produit
Description
Espèces réactives
Application
Anti-CPXCR1 antibody produced in mouse, purified immunoglobulin, buffered aqueous solution,
Espèces réactives
human
Application
immunofluorescence
western blot
Anti-CPXCR1 antibody produced in rabbit, IgG fraction of antiserum,
Espèces réactives
human
Application
western blot

esiRNA

Référence du produit
Description
Espèce(s)
MISSION® esiRNA, targeting mouse Cpxcr1,
Espèce(s)
mouse