FGF-2 Polyclonal Antibody
¥680.00
- 产品信息
商品描述
靶点-Target
NDUFS7
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)
24kD
推荐稀释比
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 NDUFS7. AA range:164-213
特异性
NDUFS7 Polyclonal Antibody detects endogenous levels of NDUFS7 protein.
基因名称
NDUFS7
蛋白名称
NADH dehydrogenase [ubiquinone] iron-sulfur protein 7 mitochondrial
别名
NDUFS7;NADH dehydrogenase [ubiquinone] iron-sulfur protein 7;mitochondrial;Complex I-20kD;CI-20kD;NADH-ubiquinone oxidoreductase 20 kDa subunit;PSST subunit
Organism-1
Human
基因ID-1
374291
SwissProt-1
O75251
Organism-2
Mouse
基因ID-2
75406
SwissProt-2
Q9DC70
背景
This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions. [provided by RefSeq, Jul 2008],
细胞定位
Mitochondrion inner membrane ; Peripheral membrane protein ; Matrix side .
