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NDUFB9 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT3014
产品名称
NDUFB9 Rabbit Polyclonal Antibody
别名
NDUFB9; LYRM3; UQOR22; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9; Complex I-B22; CI-B22; LYR motif-containing protein 3; NADH-ubiquinone oxidoreductase B22 subunit
类别
常规抗体
基因名称
NDUFB9
蛋白名称
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9
推荐应用
WB
反应种属
Human,Rat,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
4715
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=4715
Human Swissprot No.
Q9Y6M9
Human Swissprot Link
http://www.uniprot.org/uniprotkb/Q9Y6M9/entry
Mouse Swissprot No.
Q9CQJ8
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q9CQJ8
免疫原
The antiserum was produced against synthesized peptide derived from human NDUFB9. AA range:102-151
特异性
NDUFB9 Polyclonal Antibody detects endogenous levels of NDUFB9 protein.
稀释度
WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:10000.. IF 1:50-200
预测分子量
22kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015],
组织表达
Astrocytoma,Brain,Colon adenocarcinoma,Kidney,Placenta,Umbi
细胞定位
Mitochondrion inner membrane ; Peripheral membrane protein ; Matrix side .
信号通路
Oxidative phosphorylation;Alzheimer's disease;Parkinson's disease;Huntington's disease;
功能
function:Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed to be not involved in catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone.,similarity:Belongs to the complex I LYR family.,subunit:Mammalian complex I is composed of 45 different subunits.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Western blot analysis of lysates from COLO205 cells and 293 cells, using NDUFB9 Antibody. The lane on the right is blocked with the synthesized peptide.

Western blot analysis of the lysates from COLO205 cells using NDUFB9 antibody.

Western Blot analysis of various cells using NDUFB9 Polyclonal Antibody diluted at 1:500

Western Blot analysis of 293 cells using NDUFB9 Polyclonal Antibody diluted at 1:500

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