ABHD11 rabbit pAb

This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11. 23. [provided by RefSeq, Mar 2016],

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

83451

Q8NFV4

Mitochondrion,

Rabbit

Human,Rat,Mouse,

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

Polyclonal

WB,ELISA

1 year

1 mg/mL

Western Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.

32kD

PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.