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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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: 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
基因别名: ABHD11; PP1226; WBSCR21
UniProt ID: (Human) Q8NFV4
Entrez Gene ID: (Human) 83451