Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Product may be used with Western Blot (Transfected lysate).
The Isotype of this product is composed of an IgG Mixture.
Immunogen sequence: MRAGQQLASM LRWTRAWRLP REGLGPHGPS FARVPVAPSS SSGGRGGAEP RPLPLSYRLL DGEAALPAVV FLHGLFGSKT NFNSIAKILA QQTGRRVLTV DARNHGDSPH SPDMSYEIMS QDLQDLLPQL GLVPCVVVGH SMGGKTAMLL ALQRPELVER LIAVDISPVE STGVSHFATY VAAMRAINIA DELPRSRARK LADEQLSSVI QDMAVRQHLL TNLVEVDGRF VWRVNLDALT QHLDKILAFP QRQESYLGPT LFLLGGNSQF VHPSHHPEIM RLFPRAQMQT VPNAGHWIHA DRPQDFIAAI RGFLV
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; sn-1-specific diacylglycerol lipase ABHD11; 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.*
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