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Overview
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CPXCR1 is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. 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.
PRODUCT INFORMATION
Antigen Species: Human
NCBI Accession No: NP_001171700.1
RNA Reference Number: NM_001184771.1
Chromosome Location: Xq21.3
cDNA size: 906bp
Vector description: This shuttle vector contains the complete ORF. It is inseted BamH I to Xho I. The gene insert contains multiple cloning sites which can be used to easily cut and transfer the gene and recombination site into your expression vector.Please contact us at for specific academic pricing.
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Overview