Anti-Human ABHD11 Polyclonal Antibody

ABHD11多克隆抗体

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. ABHD11 (Abhydrolase Domain Containing 11) is a Protein Coding gene. Diseases associated with ABHD11 include Williams-Beuren Syndrome. GO annotations related to this gene include hydrolase activity and hydrolase activity, acting on ester bonds.
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基本信息

数据文档 查看数据文档
货号 PA02951
规格 100μl
宿主 Rabbit
免疫原 Synthesized peptide derived from the Internal region of human ABHD11
特异性 Ubiquitously expressed.
亚型 IgG
反应性 Human
克隆
Uniprot Q8NFV4
浓度 1mg/mL
推荐稀释度 WB 1:500-1:2000, ELISA 1:20000
配方
应用范围 WB,ELISA
别名 PP1226,ABHD11 abhydrolase domain containing 11,Abhydrolase domain-containing protein 11,WBSCR21,Williams-Beuren syndrome chromosomal region 21 protein
保存条件 冻干产品: 2 - 8°C保存5年; 液体: -20°C保存2年.
注意 仅用于科学研究, 不能用于疾病诊断.

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