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产地 | 中国 |
品牌 | 爱必信(absin) |
货号 | abs136873 |
保存条件 | 见爱必信官网 |
应用范围 | 见爱必信官网 |
抗体名 | PEX19 |
是否单克隆 | 否 |
克隆性 | 见爱必信官网 |
靶点 | 见爱必信官网 |
适应物种 | 见爱必信官网 |
形态 | 见爱必信官网 |
宿主 | 见爱必信官网 |
包装规格 | 50ug,100ug |
纯度 | % |
亚型 | 见爱必信官网 |
标识物 | 见爱必信官网 |
浓度 | 见爱必信官网% |
免疫原 | 见爱必信官网 |
是否进口 | 否 |
公告提醒:爱必信所有产品和服务仅用于科学研究,不用于临床应用及其他用途提供产品和服务(也不为任何个人提供产品和服务)!
抗体描述: 产品名称:Rabbit anti-PEX19 Polyclonal Antibody 产品别名:PEX19抗体 宿主:Rabbit 反应种属:Human;Mouse;Rat 克隆性:Polyclonal Antibody 保存方法:Store at -20 °C for one year. Avoid repeated freeze/thaw cycles 产品描述:This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants. 用途范围: WB 1:500-1:2000, IHC 1:50-1:200, IF/ICC 1:100-1:500, ELISA(peptide) 1:20000-1:40000
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