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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Immunogen sequence: RFVWRVNLDA LTQHLDKILA FPQRQESYLG PTLFLLGGNS QFVHPSHHPE IMRLFPRAQM QTVPNAGHWI HADRPQDFIA AIRGFLV
Highest antigen sequence identity to the following orthologs: Mouse - 70%, Rat - 70%.
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 form D; WBSCR21 form E; Williams Beuren syndrome chromosome region 21
Gene Aliases: 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.*
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