Mouse Recombinant Monoclonal iNOS antibody. Carrier free. Suitable for WB, ICC/IF and reacts with Mouse samples. Cited in 1 publication.
IgG2b
Mouse
pH: 7.2 - 7.4
Constituents: 100% PBS
Liquid
Monoclonal
WB | ICC/IF | |
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Mouse | Tested | Tested |
Species | Dilution info | Notes |
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Species Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info - | Notes - |
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Produces nitric oxide (NO) which is a messenger molecule with diverse functions throughout the body (PubMed:7504305, PubMed:7531687, PubMed:7544004, PubMed:7682706). In macrophages, NO mediates tumoricidal and bactericidal actions. Also has nitrosylase activity and mediates cysteine S-nitrosylation of cytoplasmic target proteins such PTGS2/COX2 (By similarity). As component of the iNOS-S100A8/9 transnitrosylase complex involved in the selective inflammatory stimulus-dependent S-nitrosylation of GAPDH on 'Cys-247' implicated in regulation of the GAIT complex activity and probably multiple targets including ANXA5, EZR, MSN and VIM (PubMed:25417112). Involved in inflammation, enhances the synthesis of pro-inflammatory mediators such as IL6 and IL8 (PubMed:19688109).
NOS2A, NOS2, NOS2A, Hepatocyte NOS, Inducible NO synthase, NOS type II, Peptidyl-cysteine S-nitrosylase NOS2, HEP-NOS, Inducible NOS, iNOS
Mouse Recombinant Monoclonal iNOS antibody. Carrier free. Suitable for WB, ICC/IF and reacts with Mouse samples. Cited in 1 publication.
IgG2b
Mouse
pH: 7.2 - 7.4
Constituents: 100% PBS
Liquid
Monoclonal
Yes
EPR16635
Affinity purification Protein A
kappa
Blue Ice
+4°C
+4°C
Do Not Freeze
This mouse monoclonal chimeric antibody (ab275330) is the carrier-free version of Anti-iNOS antibody [EPR16635] - Mouse IgG2b (Chimeric) ab210823. The isotype is IgG2b.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
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.
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.
This supplementary information is collated from multiple sources and compiled automatically.
Inducible Nitric Oxide Synthase commonly referred to as iNOS or NOS2 is an important enzyme in the production of nitric oxide (NO) from L-arginine. This enzyme has a molecular weight of approximately 130 kDa and is expressed in various cell types including macrophages and hepatocytes. iNOS becomes active in response to inflammatory stimuli and can produce large amounts of NO for extended periods. Western blotting and iNOS ELISA kits are frequently used methods to detect and quantify the presence and activity of iNOS in different biological samples.
INOS plays a significant role in the immune system by participating in the defense against pathogens. The enzyme is part of a molecular complex that generates NO which acts as a signaling molecule and has antimicrobial properties. iNOS activity is induced during immune responses and contributes to the elimination of bacteria and viruses through the production of reactive nitrogen species. Its expression is tightly regulated by cytokines and other signaling molecules that modulate the extent of its action.
INOS integrates into the nitric oxide signaling pathway and is closely associated with inflammatory pathways. NO serves as a messenger within the nitric oxide signaling pathway facilitating processes like vasodilation and neurotransmission. iNOS works alongside other proteins such as cytokines like interferon-gamma that elevate its activity during inflammation and immune responses. The regulation of iNOS expression and activity plays an essential role in maintaining immune homeostasis and ensuring proper response to infections.
INOS is linked to conditions characterized by excessive inflammation such as rheumatoid arthritis and sepsis. In these diseases overproduction of nitric oxide by iNOS can lead to tissue damage and exacerbate symptoms. Additionally iNOS is associated with the protein TNF-alpha as its expression is often driven by inflammatory mediators during disease states. Understanding the role of iNOS in such conditions provides insights into potential therapeutic targets for managing inflammatory diseases.
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We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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This data was developed using Anti-iNOS antibody [EPR16635] ab178945, the same antibody clone in the original rabbit isotype.
Lanes 1 - 2: Western blot - Anti-iNOS antibody [EPR16635] – Mouse IgG2b (Chimeric) (Anti-iNOS antibody [EPR16635] - Mouse IgG2b (Chimeric) ab210823) at 1/1000 dilution
Lanes 1 - 2: Western blot - Anti-iNOS antibody [EPR16635] (Anti-iNOS antibody [EPR16635] ab178945) at 1/1000 dilution
Lane 1: Untreated L6 (rat skeletal muscle myoblast) whole cell lysate at 20 µg
Lane 2: L6 treated with 50 ng/ml IL-1 beta, 20 ng/ml TNF-alpha and 100U/ml IFN-gamma for 24 h, whole cell lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Predicted band size: 131 kDa
Observed band size: 131 kDa
This data was developed using Anti-iNOS antibody [EPR16635] ab178945, the same antibody clone in the original rabbit isotype. Anti-iNOS antibody [EPR16635] - Mouse IgG2b (Chimeric) ab210823 is also the same antibody clone in a different buffer formulation.
ELISA analysis of House mouse iNOS recombinant protein at 1000 ng/mL with Anti-iNOS antibody [EPR16635] ab178945. An Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/2500 dilution was used as the secondary antibody.
This data was developed using Anti-iNOS antibody [EPR16635] ab178945, the same antibody clone in the original rabbit isotype. Anti-iNOS antibody [EPR16635] - Mouse IgG2b (Chimeric) ab210823 is also the same antibody clone in a different buffer formulation.
Anti-iNOS antibody [EPR16635] ab178945 stained in Raw264.7 cells. Untreated and LPS treated (1ug/ml, 24 hours) cells were fixed with 100% methanol (5min) at room temperature and incubated with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% triton for 1h at room temperature to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody Anti-iNOS antibody [EPR16635] - Mouse IgG2b (Chimeric) ab210823 at 5μg/ml overnight at +4°C then detected with an Alexa Fluor® 488 goat anti-mouse secondary antibody (Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) preadsorbed ab150117) at a 1/1000 dilution (shown in green). Alexa Fluor® 594 Anti-beta Tubulin antibody [EPR16774] ab206369 (Rabbit monoclonal [EPR16774] to beta Tubulin Alexa Fluor® 594) was used as a counterstaining at a 1/200 dilution for 1hour at room temperature (pseudo-colored red). DAPI was used to stain the cell nuclei (colored blue) at a concentration of 1.43μM for 1hour at room temperature.
This data was developed using Anti-iNOS antibody [EPR16635] - Mouse IgG2b (Chimeric) ab210823, the same antibody clone in a different buffer formulation.
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 3% milk before being incubated with Anti-iNOS antibody [EPR16635] - Mouse IgG2b (Chimeric) ab210823 (lane 1) and Anti-iNOS antibody [EPR16635] ab178945 (lane 2) overnight at 4°C. Antibody binding was detected using an anti-mouse (lane 1) and anti-rabbit (lane 2) antibody conjugated to HRP, and visualised using ECL development solution ECL Substrate Kit (High Sensitivity) ab133406.
All lanes: Western blot - Anti-iNOS antibody [EPR16635] – Mouse IgG2b (Chimeric) (Anti-iNOS antibody [EPR16635] - Mouse IgG2b (Chimeric) ab210823) at 5 µg
All lanes: RAW 264.7 whole cell lysate treated with 0.1 µg/mL LPS for 6 hours at 10 µg
Lane 1: Goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP) at 1/5000 dilution
Lane 2: Peroxidase AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/50000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 131 kDa
Observed band size: 131 kDa
Exposure time: 8min
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