Rabbit polyclonal antibody to ABHD11This 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. [provided by RefSeq]
Immunogen
The antiserum was produced against synthesized peptide derived from human ABHD11.
Key Feature
Clonality
Polyclonal
Host Species
Rabbit
Tested Applications
ELISAWB
ELISA: 1:20000Optimal dilutions should be determined experimentally by the end user.:
Species Reactivity
Human
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Gene Synonyms
EC 3... EC 3.-.-.- WilliamsBeuren syndrome chromosomal region 21 protein Abhydrolase domaincontaining protein 11 ABHD11 EC3... Williams-Beuren syndrome chromosomal region 21 protein Abhydrolase domain-containing protein 11 WilliamsBeuren syndrome c
Target
ABHD11
Molecular Weight(MW)
34 kDa (note)
Tissue Specificity
ABHD11 Antibody detects endogenous levels of total ABHD11 protein.
Application
Application
Western blot analysis of extracts from COLO/HuvEc cells, using ABHD11 Antibody. The lane on the right is treated with the synthesized peptide.
Application Notes
ELISA: 1:20000Optimal dilutions should be determined experimentally by the end user.:
Additional Information
Form
Liquid
Storage Instructions
Store at -20 degrees Celcius. Product is stable for at least 1 year.
Storage Buffer
Phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.