ABHD11 rabbit polyclonal, anti-human, mouse, rat

Backgroud: 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],caution:It is uncertain whether Met-1 or Met-10 is the initiator.,sequence caution:Wrong choice of frame.,similarity:Belongs to the AB hydrolase superfamily.,tissue specificity:Ubiquitously expressed.,

Synonyms: ABHD11, WBSCR21, PP1226, Abhydrolase domain-containing protein 11, Williams-Beuren syndrome chromosomal region 21 protein

Gene Name: ABHD11

Gene ID: 83451

SwissProt ID: Q8NFV4

Purification: Affinity purification

Storage: Store at 4°C short term. Aliquot and store at -20°C for 12 months. Avoid freeze/thaw cycles.