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NDUFS7 Polyclonal Antibody

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说明书下载
货号: PD4642
货期: 现货
价格: 50μL/960;100μL/1600;200μL/2560
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靶点: NDUFS7
应用: IHC,IF,ELISA
反应性 : Human,Mouse,Rat
宿主物种 : Rabbit
MW(CalcμLated) : 24kD
同种型-Isotype : IgG

隐藏域元素占位

详细信息

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

抗原&靶点信息

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

数据库链接:

Organism

基因 ID

SwissProt

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 .

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