ABHD11 Polyclonal Antibody

Ab type

Primary antibody

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.

Reactivity

Human

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Immunogen

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

Storage Stability

-20°C for one year

Concentration

1 mg/ml

MolecularWeight_Da

34690

synonyms

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