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Anti-Human ABHD11 Polyclonal Antibody

Categories: [ Antibodies][ Polyclonal Antibodies]
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. ABHD11 (Abhydrolase Domain Containing 11) is a Protein Coding gene. Diseases associated with ABHD11 include Williams-Beuren Syndrome. GO annotations related to this gene include hydrolase activity and hydrolase activity, acting on ester bonds.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA02951
Size 100μl
Host Type Rabbit
Immunogen Synthesized peptide derived from the Internal region of human ABHD11
Specificity Ubiquitously expressed.
Isotype IgG
Reacitivity Human
Clone
Uniprot Q8NFV4
Concentration 1mg/mL
Dilution WB 1:500-1:2000, ELISA 1:20000
Formulation
Application WB,ELISA
Other Names PP1226,ABHD11 abhydrolase domain containing 11,Abhydrolase domain-containing protein 11,WBSCR21,Williams-Beuren syndrome chromosomal region 21 protein
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.
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