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Human ABHD11 | |
Rabbit | |
Human (tested or 100% immunogen sequence identity) | |
IgG Polyclonal | |
Unconjugated | |
Immunoaffinity purified | |
Unmodified |
ABHD11 antibody was raised against synthetic peptide from human ABHD11 (aa154-203). | |
aa154-203 | |
ABHD11 Antibodyantibody detects endogenous levels of ABHD11. |
PBS, pH 7.4, 150 mM sodium chloride, 0.02% sodium azide, 50% glycerol | |
Store at -20°C. | |
For research use only. |
ABHD11 Antibody, WBSCR21 Antibody, PP1226 Antibody
ABHD11 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.