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Peroxin 3 Polyclonal Antibody

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说明书下载
货号: PD4101
货期: 现货
价格: 50μL/960;100μL/1600;200μL/2560
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靶点: Peroxin 3
应用: WB,ELISA,IHC
反应性 : Human,Mouse,Rat
宿主物种 : Rabbit
MW(Observed): 42kD
同种型-Isotype : IgG

隐藏域元素占位

详细信息

推荐稀释比 : WB 1:500-2000;IHC 1:50-300;ELISA 1:2000-20000
组成 : Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
纯化工艺 : The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存 : -15°C to -25°C/1 year(Do not lower than -25°C
浓度 : 1 mg/ml
克隆性 : Polyclonal

抗原&靶点信息

特异性 : Peroxin 3 Polyclonal Antibody detects endogenous levels of Peroxin 3 protein.
基因名称 : PEX3
蛋白名称 : Peroxisomal biogenesis factor 3
别名 : PEX3;Peroxisomal biogenesis factor 3;Peroxin-3;Peroxisomal assembly protein PEX3

数据库链接:

Organism

基因 ID

SwissProt

背景:

The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. 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. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular 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 Zellweger syndrome (ZWS). [provided by RefSeq, Oct 20

细胞定位 : Peroxisome membrane ; Multi-pass membrane protein .

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