Anti-NCF1/p47-phox antibody [EPR27205-231] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal NCF1/p47-phox antibody. Carrier free. Suitable for WB, ICC/IF, Flow Cyt (Intra) and reacts with Mouse, Rat samples.
View Alternative Names
Neutrophil cytosol factor 1, NCF-1, 47 kDa neutrophil oxidase factor, NCF-47K, Neutrophil NADPH oxidase factor 1, p47-phox, Ncf1
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-NCF1/p47-phox antibody [EPR27205-231] - BSA and Azide free (AB308257)
This data was produced using ab308256, the same clone but in a different formulation. Immunofluorescent analysis of 80% Methanol-fixed, 0.1% Triton X-100 permeabilized RAW 264.7 (mouse abelson murine leukemia virus-induced tumor macrophage) cells labelling NCF1/p47-phox with ab308256 at 1/250 dilution (2.004 ug/ml) followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (2 ug/ml) (Green). Confocal image showing cytoplasmic and weak nuclear staining in RAW 264.7 cell line, no staining was observed in HL-1 cell line. Low expression control : HL-1. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 ug/ml) (Red). The nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (2 ug/ml).
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-NCF1/p47-phox antibody [EPR27205-231] - BSA and Azide free (AB308257)
This data was produced using ab308256, the same clone but in a different formulation. Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized HL-1 (mouse atrial muscle cell) (Left panel) compared to RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) (Right panel) cells labelling NCF1/p47-phox with ab308256 at 1/500 dilution (0.1 ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody. Cells were stained with rabbit IgG or ab308256
- WB
Supplier Data
Western blot - Anti-NCF1/p47-phox antibody [EPR27205-231] - BSA and Azide free (AB308257)
This data was produced using ab308256, the same clone but in a different formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. Low expression : HL-1. The Lane 3 was developed using a high sensitivity ECL substrate. In lanes 1-2, the lysates were stored at -80°C prior to Western Blotting. The bands beneath the target band (32 kDa) are likely to be degradation products. In lane 3, the lysate was freshly made and used for Western Blotting immediately to minimize protein degradation. In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds.
All lanes:
Western blot - Anti-NCF1/p47-phox antibody [EPR27205-231] (<a href='/en-us/products/primary-antibodies/ncf1-p47-phox-antibody-epr27205-231-ab308256'>ab308256</a>) at 1/1000 dilution
Lane 1:
RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 20 µg
Lane 2:
HL-1 (mouse atrial muscle cell) whole cell lysate at 20 µg
Lane 3:
RAW 264.7 whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 44 kDa
Observed band size: 45 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-NCF1/p47-phox antibody [EPR27205-231] - BSA and Azide free (AB308257)
This data was produced using ab308256, the same clone but in a different formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. Low expression : skeletal muscle, brain. In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 180 seconds.
All lanes:
Western blot - Anti-NCF1/p47-phox antibody [EPR27205-231] (<a href='/en-us/products/primary-antibodies/ncf1-p47-phox-antibody-epr27205-231-ab308256'>ab308256</a>) at 1/1000 dilution
Lane 1:
Mouse lymph node tissue lysate at 20 µg
Lane 2:
Mouse spleen tissue lysate at 20 µg
Lane 3:
Mouse skeletal muscle tissue lysate at 20 µg
Lane 4:
Mouse brain tissue lysate at 20 µg
Lane 5:
Rat spleen tissue lysate at 20 µg
Lane 6:
Rat skeletal muscle tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 44 kDa
Observed band size: 45 kDa
false
Exposure time: 180s
Related conjugates and formulations (1)
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Anti-NCF1/p47-phox antibody [EPR27205-231]
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
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.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com