Background:

ABHD11 encodes a protein (abhydrolase domain containing 11) containing an alpha/beta hydrolase fold domain. ABHD11 is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.

Classification:

Primary antibody

Alternative names:

ABHD11; WBSCR21; PP1226; Abhydrolase domain-containing protein 11; Williams-Beuren syndrome chromosomal region 21 protein

Species reactivity:

Human

Host:

Rabbit

Isotype:

IgG

Immunogen:

The antiserum was produced against synthesized peptide derived from human ABHD11. AA range:161-210

Concentration:

1 mg/ml

Molecular weight:

34690

Applications:

WB, ELISA

Storage:

-20°C for one year

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