FGF-2 Polyclonal Antibody
¥680.00
- 产品信息
商品描述
靶点-Target
NDUFS6
反应性
Human,Mouse,Rat
应用
IHC,IF,ELISA
宿主物种-Host Species
Rabbit
同种型-Isotype
IgG
修饰-Modification
Unmodified
MW(Calculated)
14kD
推荐稀释比
IHC 1:100-1:300;ELISA 1:10000;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 NDUFS6. AA range:75-124
特异性
NDUFS6 Polyclonal Antibody detects endogenous levels of NDUFS6 protein.
基因名称
NDUFS6
蛋白名称
NADH dehydrogenase [ubiquinone] iron-sulfur protein 6 mitochondrial
别名
NDUFS6;NADH dehydrogenase [ubiquinone] iron-sulfur protein 6;mitochondrial;Complex I-13kD-A;CI-13kD-A;NADH-ubiquinone oxidoreductase 13 kDa-A subunit
Organism-1
Human
基因ID-1
4726
SwissProt-1
O75380
Organism-2
Mouse
基因ID-2
407785
SwissProt-2
P52503
Organism-3
Rat
基因ID-3
29478
SwissProt-3
P52504
背景
This gene encodes a subunit of the NADH:ubiquinone oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. This complex functions in the transfer of electrons from NADH to the respiratory chain. The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction. Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders.[provided by RefSeq, Oct 2009],
细胞定位
Mitochondrion inner membrane ; Peripheral membrane protein ; Matrix side .
