ABHD11 Antibody

Additional Information:
Introduction Abhydrolase domain-containing protein 11 also known as Will syndrome chromosomal region 21 protein (WBSCR21) is an enzyme that in humans is encoded by the ABHD11 gene. This gene encodes a protein containing an alpha/beta hydrolase fold domain. This gene is deleted in Will syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript var have been described, but their biological validity has not been determined. |ABHD11 Polyclonal Antibody Immunogen: The antiserum was produced against synthesized peptide derived from human ABHD11. Purification: The antibody was affinity-purified from rabbit anti-serum by immunogenic peptide affinity-chromatography. Applications: WB: 1:500~1:1000; ELISA: 1:10000. Specificity/Sensitivity: ABHD11 antibody detects endogenous levels of ABHD11. Form of Antibody: Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150 mM NaCl, 0.02% sodium azide and 50% glycerol. Storage/Stability: Stable for 1 year at -20°C and 3 months at 4°C. For maximum recovery of the product, centrifuge the original v after thawing and before removing the cap. Aliquot to avoid repeated freezing and thawing.