|Flow Cytometry (Flow)||1:10-1:50|
|Western Blot (WB)||1:1000|
|Tested Species reactivity||Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||KLH conjugated synthetic peptide between 176-205 amino acids from the central region of human ABHDB|
|Purification||Antigen affinity chromatography|
|Contains||0.09% sodium azide|
|Storage conditions||-20° C, Avoid Freeze/Thaw Cycles|
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Abhydrolase domain-containing protein 11; Alpha/beta hydrolase domain-containing protein 11; Protein ABHD11; WBSCR21; Williams Beuren syndrome chromosome region 21; Williams-Beuren syndrome chromosomal region 21 protein
Gene Aliases: ABHD11; PP1226; WBSCR21
UniProt ID: (Human) Q8NFV4
Entrez Gene ID: (Human) 83451
If an Invitrogen™ antibody doesn’t perform as described on our website or datasheet, we’ll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Get expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.