Anti-NCF1/p47-phox (phospho S304) antibody
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- WB
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Western blot - Anti-NCF1/p47-phox (phospho S304) antibody (AB63554)
All lanes:
Western blot - Anti-NCF1/p47-phox (phospho S304) antibody (ab63554) at 1/500 dilution
Lane 1:
extracts from COS7 cells treatedwith UV (15mins) at 30 µg
Lane 2:
A549 cells extracts at 30 µg
Lane 3:
A549 cells extracts at 30 µg with immunizing peptide
Predicted band size: 44 kDa
Observed band size: 45 kDa
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- WB
CiteAb
Western blot - Anti-NCF1/p47-phox (phospho S304) antibody (AB63554)
NCF1/p47-phox (phospho S304) western blot using anti-NCF1/p47-phox (phospho S304) antibody ab63554. Publication image and figure legend from Sowrirajan, B., Saito, Y., et al., 2017, Sci Rep, PubMed 28240310.
ab63554 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab63554 please see the product overview.
The expression of p47phox is increased in IL-27-induced macrophages (I-Mac).Monocytes were differentiated into macrophages in the absence (M-Mac) or presence of IL-27 (I-Mac). After differentiation, cells were incubated with or without IL-27. (a) M-mac, I-Mac, untreated M-Mac and IL-27-treated M-Mac were stimulated with or without 100 ng/ml PMA for 30 min at 37 °C and then ROS activity was measured by detection of secreted H2O2. Data shown represent means ± SD of triplicate samples. (b) The expression levels of p47phox were determined by western blot for M-Mac, I-Mac, untreated M-Mac and IL-27-treated M-Mac. (c) M-Mac and I-Mac were stimulated with or without PMA for 30 min, and then cell lysates were subjected to 2D gel electrophoresis. Expression of p47phox was detected by anti-p47phox and anti-phosphorylated S304 p47phox antibodies. (d) Whole cell lysates of M-Mac and I-Mac were prepared using RIPA buffer. Western blot analyses were performed using anti-SOD1, SOD2, SOD3 or anti-β-actin antibodies. The intensity of the band was analyzed by NIH Image J and normalized each SOD intensity with β-Actin.
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This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The NCF1/p47-phox protein plays a critical role in host defense by generating ROS which are essential for microbial killing. NCF1 is an integral part of the NADPH oxidase complex along with other subunits such as p67-phox p40-phox gp91-phox and p22-phox. When stimulated NCF1 interacts with these subunits to form an active enzyme complex that transfers electrons from NADPH to oxygen producing superoxide anion and other ROS.
Pathways
The NCF1/p47-phox component participates mainly in the NADPH oxidase activation pathway and the respiratory burst pathway. NCF1 is connected to the RAC2 GTPase which upon activation stimulates the assembly and activation of the NADPH oxidase complex at the plasma membrane. This pathway is key for the innate immune response and effective clearance of pathogens by phagocytic cells.
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