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p47-phox (phospho Ser359) Polyclonal Antibody
p47-phox (phospho Ser359) Polyclonal Antibody
p47-phox (phospho Ser359) Polyclonal Antibody
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商品属性

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 Gene Id:653361

Human Swiss Prot No:P14598

Mouse Swiss Prot No:Q09014

Immunogen:The antiserum was produced against synthesized peptide derived from human p47 phox around the phosphorylation site of Ser359. AA range:331-380

Specificity:Phospho-p47-phox (S359) Polyclonal Antibody detects endogenous levels of p47-phox protein only when phosphorylated at S359.

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. IF 1:200 - 1:1000. ELISA: 1:5000. Not yet tested in other applications.

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):45kD

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).

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