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Rabbit Anti-phospho-NCF1 (Ser359)antibody
Rabbit Anti-phospho-NCF1 (Ser359)antibody
phospho-NCF1(Ser359); phospho-p47 phox(Ser359); NCF1 (phospho S359); 47 kDa autosomal chronic granulomatous disease protein; 47 kDa neutrophil oxidase factor; NADPH oxidase organizer 2; NCF 47K; Neutrophil cytosol factor 1; Neutrophil cytosolic factor 1;
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  • NO.:SL11445R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,Rat,
    Applications:WB ELISA IHC-F ICC IF
    concentration:1mg/ml
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Product Name phospho-NCF1 (Ser359)
Chinese Name 磷酸化嗜中性粒细胞胞浆因子1抗体
Alias phospho-NCF1(Ser359); phospho-p47 phox(Ser359); NCF1 (phospho S359); 47 kDa autosomal chronic granulomatous disease protein; 47 kDa neutrophil oxidase factor; NADPH oxidase organizer 2; NCF 47K; Neutrophil cytosol factor 1; Neutrophil cytosolic factor 1; Neutrophil NADPH oxidase factor 1; Nox organizer 2; Nox organizing protein 2; NOXO2; p47 phox; p47phox; ;SH3 and PX domain containing protein 1A; SH3PXD1A; NADPH oxidase p47 phox; NCF1_HUMAN.  
literatures
Specific References  (3)     |     SL11445R has been referenced in 3 publications.
[IF=7.285] Shen, Liang. et al. Angiotensin Type 2 Receptor Pharmacological Agonist Relieves Neurocognitive Deficits via Reducing Neuroinflammation and Microglial Engulfment of Dendritic Spines. J NEUROIMMUNE PHARM. 2022 Dec;:1-17  WB ;  Mouse.  
[IF=4.776] Arifen, Nahida. et al. Sirtuin1 inhibitor attenuates hypertension in spontaneously hypertensive rats: role of Giα proteins and nitroxidative stress. J HYPERTENS. 2022 Jul;40(7):1314-1326  WB ;  Rat.  
[IF=3.26] Chen, Gangling, et al. "Limb Remote Ischemic Postconditioning Reduces Ischemia-Reperfusion Injury by Inhibiting NADPH Oxidase Activation and MyD88-TRAF6-P38MAP-Kinase Pathway of Neutrophils." International Journal of Molecular Sciences 17.12 (2016): 1971.  WB ;  Rat.  
Product Type Phosphorylated anti 
Research Area Tumour  Cell biology  Signal transduction  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human, Rat, 
Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 45kDa
Cellular localization cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthesised phosphopeptide derived from human NCF1 around the phosphorylation site of Ser359: QR(p-S)K 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail The heredity chronic granulomatous disease (CGF) has been linked to mutations in p47-phox and p67-phox. The cytosolic proteins p47-phox and p67-phox, also designated neutrophil cytosol factor (NCF)1 and NCF2, respectively, are required for activation of the superoxide-producing NADPH oxidase in neutrophils and other phagocytic cells. During activation of the NADPH oxidase, p47-phox and p67-phox migrate to the plasma membrane where they associate with cytochrome b558 and the small G protein Rac to form the functional enzyme complex. Both p47-phox and p67-phox contain two Src homology 3 (SH3) domains. The C-terminal SH3 domain of p67-phox has been shown to interact with the proline-rich domain of p47-phox, suggesting that p47-phox may faciliate the transport of p67-phox to the membrane.

Function:
NCF2, NCF1, and a membrane bound cytochrome b558 are required for activation of the latent NADPH oxidase (necessary for superoxide production).

Subunit:
Interacts with NOXA1. Interacts with ADAM15. Interacts with TRAF4. Interacts with FASLG.

Subcellular Location:
Cytoplasm.

Post-translational modifications:
Phosphorylated by PRKCD; phosphorylation induces activation of NCF1 and NADPH oxidase activity.

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.

Similarity:
Contains 1 PX (phox homology) domain.
Contains 2 SH3 domains.

SWISS:
P14598

Gene ID:
653361

Database links:

Entrez Gene: 281345 Cow

Entrez Gene: 653361 Human

Entrez Gene: 17969 Mouse

Entrez Gene: 100134857 Pig

Entrez Gene: 100008803 Rabbit

Entrez Gene: 114553 Rat

Omim: 608512 Human

SwissProt: O77774 Cow

SwissProt: P14598 Human

SwissProt: Q09014 Mouse

Unigene: 647047 Human

Unigene: 655201 Human

Unigene: 425296 Mouse

Unigene: 38575 Rat



Product Picture
Sample:
Lane 1: Rat Lymph node tissue lysates
Lane 2: Human Raji cell lysates
Lane 3: Human THP-1 cell lysates
Primary: Anti- phospho-NCF1 (Ser359) (SL11445R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 45 kDa
Observed band size: 47 kDa

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