Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
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Antibody detects endogenous levels of total ABHD11.
ABHDB encodes a protein containing an alpha/beta hydrolase fold domain. This protein is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Abhydrolase domain-containing protein 11; Alpha/beta hydrolase domain-containing protein 11; sn-1-specific diacylglycerol lipase ABHD11; Williams Beuren syndrome chromosome region 21; Williams-Beuren syndrome chromosomal region 21 protein
Gene Aliases: ABHD11; PP1226; WBSCR21
UniProt ID: (Human) Q8NFV4
Entrez Gene ID: (Human) 83451
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