p47-phox Polyclonal Antibody

    • Catalog No.:YT3520
    • Applications:WB;IHC;IF;ELISA
    • Reactivity:Human;Mouse;Rat
      • Target:
      • p47-phox
      • Fields:
      • >>Chemokine signaling pathway;>>Phagosome;>>Osteoclast differentiation;>>Neutrophil extracellular trap formation;>>Fc gamma R-mediated phagocytosis;>>Leukocyte transendothelial migration;>>Prion disease;>>Leishmaniasis;>>Chemical carcinogenesis - reactive oxygen species;>>Diabetic cardiomyopathy;>>Lipid and atherosclerosis;>>Fluid shear stress and atherosclerosis
      • Gene Name:
      • NCF1
      • Protein Name:
      • Neutrophil cytosol factor 1
      • Human Swiss Prot No:
      • P14598
      • Mouse Swiss Prot No:
      • Q09014
      • Immunogen:
      • The antiserum was produced against synthesized peptide derived from human p47 phox. AA range:341-390
      • Specificity:
      • p47-phox Polyclonal Antibody detects endogenous levels of p47-phox protein.
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Polyclonal, Rabbit,IgG
      • Dilution:
      • WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:5000.. IF 1:50-200
      • Purification:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • Concentration:
      • 1 mg/ml
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • NCF1;NOXO2;SH3PXD1A;Neutrophil cytosol factor 1;NCF-1;47 kDa autosomal chronic granulomatous disease protein;47 kDa neutrophil oxidase factor;NCF-47K;Neutrophil NADPH oxidase factor 1;Nox organizer 2;Nox-organizing protein 2;SH3
      • Observed Band(KD):
      • 44kD
      • Background:
      • The protein encoded by this gene is a 47 kDa cytosolic subunit of neutrophil NADPH oxidase. This oxidase is a multicomponent enzyme that is activated to produce superoxide anion. Mutations in this gene have been associated with chronic granulomatous disease. [provided by RefSeq, Jul 2008],
      • Function:
      • disease:Defects in NCF1 are the cause of chronic granulomatous disease autosomal recessive cytochrome-b-positive type 1 (CGD1) [MIM:233700]. Chronic granulomatous disease is a genetically heterogeneous disorder characterized by the inability of neutrophils and phagocytes to kill microbes that they have ingested. Patients suffer from life-threatening bacterial/fungal infections.,function:NCF2, NCF1, and a membrane bound cytochrome b558 are required for activation of the latent NADPH oxidase (necessary for superoxide production).,online information:NCF1 deficiency database,similarity:Contains 1 PX (phox homology) domain.,similarity:Contains 2 SH3 domains.,subunit:Interacts with NOXA1.,
      • Subcellular Location:
      • Cytoplasm, cytosol . Membrane ; Peripheral membrane protein ; Cytoplasmic side .
      • Expression:
      • Detected in peripheral blood monocytes and neutrophils (at protein level).
      • Products Images
      • Western Blot analysis of various cells using p47-phox Polyclonal Antibody
      • Western Blot analysis of COLO205 cells using p47-phox Polyclonal Antibody
      • Immunohistochemistry analysis of paraffin-embedded human tonsil tissue, using p47 phox Antibody. The picture on the right is blocked with the synthesized peptide.
      • Western blot analysis of lysates from HT-29, COLO205, and HepG2 cells, , using p47 phox Antibody. The lane on the right is blocked with the synthesized peptide.
      • Western blot analysis of the lysates from COLO205 cells using p47 phox antibody.