Mouse Recombinant Monoclonal IDH1 mutated R132G antibody. Carrier free. Suitable for ELISA, WB and reacts with Human samples. Cited in 2 publications.
Constituents: 100% PBS
ELISA | WB | |
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Human | Tested | Tested |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info - | Notes - |
Catalyzes the NADP(+)-dependent oxidative decarboxylation of isocitrate (D-threo-isocitrate) to 2-ketoglutarate (2-oxoglutarate), which is required by other enzymes such as the phytanoyl-CoA dioxygenase (PubMed:10521434, PubMed:19935646). Plays a critical role in the generation of NADPH, an important cofactor in many biosynthesis pathways (PubMed:10521434). May act as a corneal epithelial crystallin and may be involved in maintaining corneal epithelial transparency (By similarity).
IDH2 mutated R172G
PICD, IDH1, Isocitrate dehydrogenase [NADP] cytoplasmic, IDH, Cytosolic NADP-isocitrate dehydrogenase, IDPc, NADP(+)-specific ICDH, Oxalosuccinate decarboxylase
Mouse Recombinant Monoclonal IDH1 mutated R132G antibody. Carrier free. Suitable for ELISA, WB and reacts with Human samples. Cited in 2 publications.
Constituents: 100% PBS
The antibody also showed the cross reactivity with other mutants of IDH1 and IDH2.
ab264085 is the carrier-free version of Anti-IDH1 (mutated R132G) + IDH2 (mutated R172G) antibody [MsMab-1] ab264055.
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.
IDH1 and IDH2 also known as isocitrate dehydrogenase 1 and 2 play important roles in cellular metabolism. IDH1 has an approximate molecular mass of 45 kDa and is primarily expressed in the cytoplasm and peroxisomes whereas IDH2 with a similar mass is mainly localized in the mitochondria. These enzymes catalyze the oxidative decarboxylation of isocitrate to alpha-ketoglutarate coupled with the conversion of NADP+ to NADPH. This reaction contributes to cellular energy production and antioxidant defense.
The IDH1 and IDH2 enzymes function by maintaining cellular redox balance and providing reductive power for biosynthesis. They also participate as part of the tricarboxylic acid (TCA) cycle where their enzymatic activity is important for the continuation of this metabolic pathway. The role of IDH1 and IDH2 within the TCA cycle ensures the efficient conversion of nutrients into energy. Their activity reflects a direct influence on central metabolic processes including lipid biosynthesis glucose metabolism and the generation of cellular building blocks.
Both IDH1 and IDH2 are fundamental components of the TCA cycle and are also involved in the reductive carboxylation pathway. Their function involves key interactions with other metabolic proteins such as alpha-ketoglutarate dehydrogenase which also feeds into the TCA cycle. Fatty acid synthesis and glutamine metabolism pathways also align with IDH1 and IDH2 functions linking them to essential cellular processes that balance energy production with biosynthetic needs.
IDH1 and IDH2 mutations have been strongly associated with gliomas and acute myeloid leukemia (AML). These mutations significantly alter the normal enzymatic activity leading to the production of the oncometabolite 2-hydroxyglutarate. This metabolite disrupts cellular metabolism and epigenetic regulation contributing to cancer progression. Furthermore the dysfunctional IDH enzymes connect with dysfunctional TET (Ten-Eleven Translocation) proteins which are involved in DNA methylation and gene expression regulation highlighting their involvement in tumorigenesis.
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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This data was developed using Anti-IDH1 (mutated R132G) + IDH2 (mutated R172G) antibody [MsMab-1] ab264055, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
The loading samples are E.coil extracts containing recombinant protein respectively.
Exposure time: 10 seconds
All lanes: Western blot - Anti-IDH1 (mutated R132G) + IDH2 (mutated R172G) antibody [MsMab-1] (Anti-IDH1 (mutated R132G) + IDH2 (mutated R172G) antibody [MsMab-1] ab264055) at 1/1000 dilution
Lane 1: His-tagged human IDH1 (aa1-414) recombinant protein at 0.01 µg
Lane 2: His-tagged human IDH1 mutated R132H (aa1-414) recombinant protein at 0.01 µg
Lane 3: His-tagged human IDH1 mutated R132G (aa1-414) recombinant protein at 0.01 µg
Lane 4: His-tagged human IDH1 mutated R132L (aa1-414) recombinant protein at 0.01 µg
Lane 5: His-tagged human IDH1 mutated R132S (aa1-414) recombinant protein at 0.01 µg
Lane 6: His-tagged human IDH1 mutated R132V (aa1-414) recombinant protein at 0.01 µg
Lane 7: His-tagged human IDH1 mutated R132C (aa1-414) recombinant protein at 0.01 µg
Lane 8: His-tagged human IDH2 (aa40-452) recombinant protein at 0.01 µg
Lane 9: His-tagged human IDH2 mutated R172M (aa40-452) recombinant protein at 0.01 µg
Lane 10: His-tagged human IDH2 mutated R172S (aa40-452) recombinant protein at 0.01 µg
Lane 11: His-tagged human IDH2 mutated R172G (aa40-452) recombinant protein at 0.01 µg
Lane 12: His-tagged human IDH2 mutated R172W (aa40-452) recombinant protein at 0.01 µg
Lane 13: His-tagged human IDH2 mutated R172K (aa40-452) recombinant protein at 0.01 µg
Lane 14: His-tagged human IDH2 mutated R140Q (aa40-452) recombinant protein at 0.01 µg
All lanes: Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution
Observed band size: 46 kDa
This data was developed using Anti-IDH1 (mutated R132G) + IDH2 (mutated R172G) antibody [MsMab-1] ab264055, the same antibody clone in a different buffer formulation.
Antigen: Human IDH1, Human IDH1(R132H), Human IDH1(R132G), Human IDH1(R132L), Human IDH1(R132S), Human IDH1(R132V), Human IDH1(R132C)).
Antigen concentration: 50 ng/ml.
Anti-IDH1 (mutated R132G) + IDH2 (mutated R172G) antibody [MsMab-1] ab264055 used at 0 - 1000 ng/ml.
Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Mouse IgG (H+L)secondary antibody was used at 1:1000 dilution.
This data was developed using Anti-IDH1 (mutated R132G) + IDH2 (mutated R172G) antibody [MsMab-1] ab264055, the same antibody clone in a different buffer formulation.
Antigen: Human IDH2, Human IDH2(R172G), Human IDH2(R172M), Human IDH2(R172S), Human IDH2(R172W), Human IDH2(R172K), Human IDH2(R140Q).
Antigen concentration: 50 ng/ml.
Anti-IDH1 (mutated R132G) + IDH2 (mutated R172G) antibody [MsMab-1] ab264055 used at 0 - 1000 ng/ml.
Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Mouse IgG (H+L)secondary antibody was used at 1:1000 dilution.
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