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ABHDB Rabbit anti-Human, Polyclonal, Invitrogen™
Rabbit Polyclonal Antibody
Supplier: Thermo Scientific PA526427
Description
ABHDB encodes a protein containing an alpha/beta hydrolase fold domain. This protein is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
Specifications
ABHDB | |
Polyclonal | |
ABHD11 | |
WBSCR21, Williams Beuren syndrome chromosome region 21, abhydrolase domain-containing protein 11, williams-Beuren syndrome chromosomal region 21 protein | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
83451 | |
-20° C, Avoid Freeze/Thaw Cycles | |
Liquid |
Flow Cytometry, Western Blot | |
Unconjugated | |
Q8NFV4 | |
ABHD11 | |
KLH conjugated synthetic peptide between 176-205 amino acids from the central region of human ABHDB | |
400 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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