Peroxin 3 Polyclonal Antibody
活动价:
市场价:¥880.00
- 50μL
- 100μL
FAB2615695
- 产品信息
商品描述
靶点-Target
Peroxin 3
反应性
Human,Mouse,Rat
应用
WB,ELISA,IHC
宿主物种-Host Species
Rabbit
同种型-Isotype
IgG
修饰-Modification
Unmodified
MW(Observed)
42kD
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
免疫原
The antiserum was produced against synthesized peptide derived from human PEX3. AA range:12-61
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
Organism-1
Human
基因ID-1
8504
SwissProt-1
P56589
Organism-2
Mouse
基因ID-2
56535
SwissProt-2
Q9QXY9
Organism-3
Rat
基因ID-3
83519
SwissProt-3
Q9JJK4
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 .





