CCDC102B Polyclonal Antibody, 50ul ssDNA Synthesis The encoded protein was originally

The encoded protein was originally described in bile ducts of liver as biliary glycoprotein

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Mutations in PEX1 have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy

CCDC102B Polyclonal Antibody, 50ul ssDNA Synthesis The encoded protein was originallyCCDC102B (coiled coil domain containing 102B), also known as AN, ACY1L or HsT1731, is a 513 amino acid protein that exists as three alternatively spliced isoforms. Widely expressed and found in multiple CNV (copy number variant) regions, CCDC102B contains the deletion breakpoint of a maternally inherited deletion, which is 2. 7 Mb in size, and maps to human chromosome 18q22. 1. CCDC102B may play a role in the pathogenesis of diaphragmatic hernia,