Rabbit Recombinant Monoclonal IRR antibody. Carrier free. Suitable for IP, WB and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
ICC/IF | IP | Flow Cyt | WB | IHC-P | |
---|---|---|---|---|---|
Human | Not recommended | Tested | Not recommended | Tested | Not recommended |
Mouse | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended |
Rat | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended |
Species | Dilution info | Notes |
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Species Mouse, Human, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Human, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human, Mouse, Rat | Dilution info - | Notes - |
Receptor with tyrosine-protein kinase activity. Functions as a pH sensing receptor which is activated by increased extracellular pH. Activates an intracellular signaling pathway that involves IRS1 and AKT1/PKB.
IRR, INSRR, Insulin receptor-related protein, IR-related receptor
Rabbit Recombinant Monoclonal IRR antibody. Carrier free. Suitable for IP, WB and reacts with Human samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
ab282736 is the carrier-free version of Anti-IRR antibody [EPR24776-127] ab273125.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
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.
The Insulin Receptor-Related Receptor (IRR) also called INSRR is a receptor tyrosine kinase that is linked structurally to the insulin receptor. This protein has a molecular mass of about 140 kDa. IRR expresses in tissues such as the kidney lung and stomach. It functions mainly as a pH sensor playing a role in regulating cellular responses to extracellular pH changes. Through its intrinsic kinase activity IRR phosphorylates specific substrates upon ligand binding initiating downstream signaling events.
IRR acts in a manner analogous to other receptor tyrosine kinases but is unique in its role as a pH sensor impacting various physiological processes. It does not usually form part of larger protein complexes but influences cellular homeostasis and adaptive responses to acidic conditions. Its activity may affect cellular growth and differentiation. Researchers have identified that IRR contributes to maintaining the pH balance in tissues where it is present which implies its importance in controlling basic cellular functions.
The IRR participates in signaling pathways that monitor and regulate pH homeostasis and related metabolic responses. It connects with the MAPK/ERK pathway which influences cell proliferation and stress responses. This connection links IRR and MAPK/ERK to processes essential for cellular adaptation to changing pH conditions. The presence of proteins like Akt which also has roles in the pathways involving insulin receptor signals suggests IRR might have related but distinct signaling functions.
The understanding of IRR's role relates to conditions such as cancer and metabolic acidosis. Changes in its activity may influence cancer progression due to its ties with cell proliferation pathways. Abnormal IRR signaling potentially impacts acidosis-related metabolic dysfunctions where IRR's regulatory action on pH becomes critical. In these contexts proteins like the insulin receptor may share overlapping functionalities with IRR as both are receptor tyrosine kinases although IRR’s specific disease links remain less characterized.
We have tested this species and application combination and it works. It is covered by our product promise.
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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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-IRR antibody [EPR24776-127] ab273125, the same antibody clone in a different buffer formulation.
IRR was immunoprecipitated from 0.35 mg HepG2 (human hepatocellular carcinoma epithelial cell) whole cell lysate with Anti-IRR antibody [EPR24776-127] ab273125 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-IRR antibody [EPR24776-127] ab273125 at 1/1000 dilution. Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (Goat Anti-Rabbit IgG H&L (HRP) ab97051) was used at 1/5000 dilution.
Lane 1: HepG2 (human hepatocellular carcinoma epithelial cell) whole cell lysate 10 μg
Lane 2: Anti-IRR antibody [EPR24776-127] ab273125 IP in HepG2 whole cell lysate
Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-IRR antibody [EPR24776-127] ab273125 in HepG2 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 3 minutes
All lanes: Immunoprecipitation - Anti-IRR antibody [EPR24776-127] (Anti-IRR antibody [EPR24776-127] ab273125)
Predicted band size: 144 kDa
Observed band size: 60 kDa
This data was developed using Anti-IRR antibody [EPR24776-127] ab273125, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration:5% NFDM/TBST
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 29156593).
Negative control: U-937.
Exposure time: 3 minutes
All lanes: Western blot - Anti-IRR antibody [EPR24776-127] (Anti-IRR antibody [EPR24776-127] ab273125) at 1/1000 dilution
Lane 1: HepG2 (Human liver hepatocellular carcinoma cell line) whole cell lysate at 20 µg
Lane 2: SH-SY5Y (human neuroblastoma epithelial cell) whole cell lysate at 20 µg
Lane 3: U-937 (human histiocytic lymphoma monocyte) 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: 144 kDa
Observed band size: 60 kDa
This data was developed using Anti-IRR antibody [EPR24776-127] ab273125, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
Exposure time: 3 minutes
All lanes: Western blot - Anti-IRR antibody [EPR24776-127] (Anti-IRR antibody [EPR24776-127] ab273125) at 1/5000 dilution
All lanes: Human heart tissue lysate at 20 µg
All lanes: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Predicted band size: 144 kDa
Observed band size: 60 kDa
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