MTCO2 (PT0068R) PT® Rabbit mAb

    • 货号:YM8036
    • 应用:WB;IHC;IF;IP;ELISA
    • 种属:Human;
      • 靶点:
      • COX2
      • 简介:
      • >>Oxidative phosphorylation;>>Metabolic pathways;>>Cardiac muscle contraction;>>Thermogenesis;>>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:
      • MT-CO2 COII COXII MTCO2
      • 蛋白名称:
      • Cytochrome c oxidase subunit 2 (Cytochrome c oxidase polypeptide II)
      • Human Gene Id:
      • 4513
      • Human Swiss Prot No:
      • P00403
      • Mouse Swiss Prot No:
      • P00405
      • 特异性:
      • endogenous
      • 组成:
      • PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
      • 来源:
      • Monoclonal, rabbit, IgG, Kappa
      • 稀释:
      • IHC 1:200-1000,WB 1:1000-5000,IF 1:200-1000,ELISA 1:5000-20000,IP 1:50-200
      • 纯化工艺:
      • Protein A
      • 储存:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • 分子量:
      • 26kD
      • 实测条带:
      • 21kD
      • 背景:
      • cofactor:Copper A.,disease:Defects in MT-CO2 are a cause of cytochrome c oxidase deficiency (COX deficiency) [MIM:220110]; also called mitochondrial complex IV deficiency. COX deficiency is a clinically heterogeneous disorder. The clinical features are ranging from isolated myopathy to severe multisystem disease, with onset from infancy to adulthood.,disease:Defects in MT-CO2 are associated with tumor formation.,function:Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1-3 form the functional core of the enzyme complex. Subunit 2 transfers the electrons from cytochrome c via its binuclear copper A center to the bimetallic center of the catalytic subunit 1.,similarity:Belongs to the cytochrome c oxidase subunit 2 family.,
      • 功能:
      • cofactor:Copper A.,disease:Defects in MT-CO2 are a cause of cytochrome c oxidase deficiency (COX deficiency) [MIM:220110]; also called mitochondrial complex IV deficiency. COX deficiency is a clinically heterogeneous disorder. The clinical features are ranging from isolated myopathy to severe multisystem disease, with onset from infancy to adulthood.,disease:Defects in MT-CO2 are associated with tumor formation.,function:Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1-3 form the functional core of the enzyme complex. Subunit 2 transfers the electrons from cytochrome c via its binuclear copper A center to the bimetallic center of the catalytic subunit 1.,similarity:Belongs to the cytochrome c oxidase subunit 2 family.,
      • 细胞定位:
      • Cytoplasmic
      • 组织表达:
      • Blood,Bone fossil,Bones,Breast cancer,Distant normal tissue,Endometrial ade

      Deciphering the performance of polo-like kinase 1 in triple-negative breast cancer progression according to the centromere protein U-phosphorylation pathway. American Journal of Cancer Research Am J Cancer Res. 2021; 11(5): 2142–2158 WB Human MDA-MB-231cell, CAL-51 cancer cell
      货号:YM8036

      Lipopolysaccharide Affects the Proliferation and Glucose Metabolism of Cervical Cancer Cells Through the FRA1/MDM2/p53 Pathway. International Journal of Medical Sciences Int J Med Sci. 2021; 18(4): 1030–1038 WB Human Hela cell, Caski cell
      货号:YM8036

      “Deciphering the performance of polo-like kinase 1 in triple-negative breast cancer progression according to the centromere protein U-phosphorylation pathway.” American journal of cancer research vol. 11,5 2142-2158. 15 May. 2021
      货号:YM8036

      Deciphering the performance of polo-like kinase 1 in triple-negative breast cancer progression according to the centromere protein U-phosphorylation pathway. American Journal of Cancer Research Am J Cancer Res. 2021; 11(5): 2142–2158 WB Human MDA-MB-231cell, CAL-51 cancer cell
      货号:YM8036

      • 产品图片
      • Various whole cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with anti-MTCO2 (PT0068R) antibody. The HRP-conjugated Goat anti-Rabbit IgG(H + L) antibody was used to detect the antibody. Lane 1: Hela Lane 2: MCF7 Predicted band size: 26kDa Observed band size: 21kDa
      • Human kidney was stained with Anti-MTCO2 (PT0068R) rabbit antibody
      • Human liver was stained with Anti-MTCO2 (PT0068R) rabbit antibody