Peroxin 7 Polyclonal Antibody
活动价:
市场价:¥880.00
- 50μL
- 100μL
FAB2615697
- 产品信息
商品描述
靶点-Target
Peroxin 7
反应性
Human,Mouse,Rat
应用
WB,IHC,IF,ELISA
宿主物种-Host Species
Rabbit
同种型-Isotype
IgG
修饰-Modification
Unmodified
MW(Observed)
40kD
推荐稀释比
WB 1:500-1:2000;IHC 1:100-1:300;ELISA 1:40000;IF 1:50-200
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 PEX7. AA range:204-253
特异性
Peroxin 7 Polyclonal Antibody detects endogenous levels of Peroxin 7 protein.
基因名称
PEX7
蛋白名称
Peroxisomal targeting signal 2 receptor
别名
PEX7;PTS2R;Peroxisomal targeting signal 2 receptor;PTS2 receptor;Peroxin-7
Organism-1
Human
基因ID-1
5191
SwissProt-1
O00628
Organism-2
Mouse
基因ID-2
18634
SwissProt-2
P97865
背景
This gene encodes the cytosolic receptor for the set of peroxisomal matrix enzymes targeted to the organelle by the peroxisome targeting signal 2 (PTS2). Defects in this gene cause peroxisome biogenesis disorders (PBDs), which are characterized by multiple defects in peroxisome function. There are at least 14 complementation groups for PBDs, with more than one 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 have been associated with PBD complementation group 11 (PBD-CG11) disorders, rhizomelic chondrodysplasia punctata type 1 (RCDP1), and Refsum disease (RD). [provided by RefSeq, Oct 2008],
细胞定位
Peroxisome . Cytoplasm .





