别名:ABHDB; abhydrolase domain containing 11; EC 3.-.-.-; PP1226; WBSCR21应用:WB
反应种属:Human
规格:50μl/100μl
Description |
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This gene 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.Merla G., Hum. Genet. 110:429-438(2002). Hillier L.W., Nature 424:157-164(2003). The MGC Project Team; Genome Res. 14:2121-2127(2004). |
Specification | |
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Aliases | ABHDB; abhydrolase domain containing 11; EC 3.-.-.-; PP1226; WBSCR21 |
Entrez GeneID | 83451; |
Swissprot | Q8NFV4 |
WB Predicted band size | 32kDa |
Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
Species Reactivity | Human |
Immunogen | Synthesized peptide derived from internal of human ABHD11. |
Formulation | Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. |
Application | |
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WB | 1/500-1/3000 |
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Western blot analysis of extracts from HUVEC cells and COLO cells, using ABHD11 antibody P42246. |
本公司的所有产品仅用于科学研究或者工业应用等非医疗目的,不可用于人类或动物的临床诊断或治疗,非药用,非食用。
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本公司的所有产品仅用于科学研究或者工业应用等非医疗目的,不可用于人类或动物的临床诊断或治疗,非药用,非食用。
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