兔抗ABHD11多克隆抗體

Background:

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. Alternatively spliced transcript variants have been described, but their biological validity has not been determined.

Applications:

WB

Name of antibody:

ABHD11

Immunogen:

Synthesized peptide derived from internal of human ABHD11.

Full name:

abhydrolase domain containing 11

Synonyms：

PP1226; WBSCR21

SwissProt:

Q8NFV4

WB Predicted band size:

35 kDa

WB Positive control:

Huvec cells and COLO cells lysates

WB Recommended dilution:

500-3000