NDUFB9 Polyclonal Antibody

    • 货号:YT3014
    • 应用:WB;IHC;IF;ELISA
    • 种属:Human;Mouse
      • 靶点:
      • NDUFB9
      • 简介:
      • >>Oxidative phosphorylation;>>Metabolic pathways;>>Thermogenesis;>>Retrograde endocannabinoid signaling;>>Non-alcoholic fatty liver disease;>>Alzheimer disease;>>Parkinson disease;>>Amyotrophic lateral sclerosis;>>Huntington disease;>>Prion disease;>>Pathways of neurodegeneration - multiple diseases;>>Chemical carcinogenesis - reactive oxygen species;>>Diabetic cardiomyopathy
      • 基因名称:
      • NDUFB9
      • 蛋白名称:
      • NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9
      • Human Gene Id:
      • 4715
      • Human Swiss Prot No:
      • Q9Y6M9
      • Mouse Swiss Prot No:
      • 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.
      • 组成:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • 来源:
      • Polyclonal, Rabbit,IgG
      • 稀释:
      • WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:10000.. IF 1:50-200
      • 纯化工艺:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • 浓度:
      • 1 mg/ml
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 其他名称:
      • 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
      • 实测条带:
      • 22kD
      • 背景:
      • 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],
      • 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.,
      • 细胞定位:
      • Mitochondrion inner membrane ; Peripheral membrane protein ; Matrix side .
      • 组织表达:
      • Astrocytoma,Brain,Colon adenocarcinoma,Kidney,Placenta,Umbi
      • 产品图片
      • 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
      • 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.
      • Immunohistochemical analysis of paraffin-embedded human liver cancer. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).