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NDUFS7 Polyclonal Antibody
货 号:
YM-A19326
规 格:
50μL;100μL
种属反应:
Human,Mouse,Rat
实验应用:
IHC,IF,ELISA
产品详情
产品名称
NDUFS7 Polyclonal Antibody
产品货号
YM-A19326
规格
50μL;100μL
种属反应
Human,Mouse,Rat
实验应用
IHC,IF,ELISA
分子量
宿主
Rabbit
同种型
IgG
修饰
Unmodified
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
克降性
Polyclonal
克隆号
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
基因ID-1
374291
SwissProt
O75251
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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