Isocitrate Dehydrogenase 1 (NADP+), Soluble (IDH1) ELISA Kits

Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. Additionally we are shipping IDH1 Antibodies (239) and IDH1 Proteins (17) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
IDH1 3417 O75874
IDH1 15926 O88844
IDH1 24479 P41562
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Top IDH1 ELISA Kits at

Showing 5 out of 29 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Delivery Price Details
Human 0.33 ng/mL 0.78 ng/mL - 50 ng/mL Typical standard curve 96 Tests 12 to 14 Days
Rat 1.35 ng/mL 3.12 ng/mL - 200 ng/mL 96 Tests 13 to 16 Days
  96 Tests 11 to 18 Days
  96 Tests 15 to 18 Days
  96 Tests 15 to 18 Days

Top referenced IDH1 ELISA Kits

  1. Human IDH1 ELISA Kit for Sandwich ELISA - ABIN6574327 : Tan, Jiang, Sun, Chen, Lv, Shao, Li, Qiu, Gao, Li, Tan, Zhou, Wang, Ding, Wang, Sun, Hang, Shi, Feng, He, He: Identification of isocitrate dehydrogenase 1 as a potential diagnostic and prognostic biomarker for non-small cell lung cancer by proteomic analysis. in Molecular & cellular proteomics : MCP 2012 (PubMed)
    Show all 3 Pubmed References

  2. Human IDH1 ELISA Kit for Sandwich ELISA - ABIN423443 : Sun, Chen, Tan, Zhang, Yao, Zhou, Li, Gao, Liu, Tan, Zhou, He, Shao, Li, Qiu, Sun, Yu, Wang, Zhao, Shi, He: Isocitrate dehydrogenase 1 is a novel plasma biomarker for the diagnosis of non-small cell lung cancer. in Clinical cancer research : an official journal of the American Association for Cancer Research 2013 (PubMed)
    Show all 3 Pubmed References

More ELISA Kits for IDH1 Interaction Partners

Human Isocitrate Dehydrogenase 1 (NADP+), Soluble (IDH1) interaction partners

  1. These results indicated that mutation of IDH1 aggravated the fatty acidinduced oxidative stress in HCT116 cells, by suppressing FAO and disrupting the mitochondrial respiratory chain. The results of the present study may provide novel insight into therapeutic strategies for the treatment of cancer types with IDH mutation.

  2. The overexpression of total and phosphorylated mTOR as well as phosphorylated rpS6 (residues 240-244) were associated with wild-type IDH1 only glioblastomas. The expression and phosphorylation of mTOR and phosphorylation of rpS6 at residues 240-244 were associated with a worse prognosis in glioblastomas.

  3. Fibulin-5 silencing in non-small-cell lung cancer cells is due to the hypermethylation of its promoter through 2-hydroxyglutarate, production of which arises from a mutation in IDH1.

  4. combined expression of Jak2V617F and mutant IDH1R132H or Idh2R140Q induces myeloproliferative neoplasm progression, alters stem/progenitor cell function, and impairs differentiation

  5. IDH1 mutation causing metabolic stress is associated with glioma.

  6. IDH1 mutation is associated with minimal residual disease assessment in acute myeloid leukemia.

  7. Heterozygous IDH1 (R132H) suppresses but hemizygous IDH1 (R132H) promotes anchorage-independent growth. Whereas genetic deletion of the wild-type allele in IDH1 (R132H) -heterozygous cells resulted in a pronounced increase in neurosphere genesis, restoration of IDH1 expression in IDH1 (R132H) -hemizygous cells led to the contrary.

  8. Alterations of EZH2, KMT2C, and CHD4 at genetic level or protein level could perturb epigenetic program, leading to malignant transformation in glioma.

  9. In most cases, IDH1, TP53 and TERTp mutation status and MGMT and ATRX protein expression levels were stable during recurrence, which may indicate that these alterations occurred early in astrocytic tumour development.

  10. XRCC1 silencing suppressed lethal fusion of dysfunctional telomeres by allowing IDH1-mutant ATRX-deficient cells to use homologous recombination.

  11. results suggest that there is no impact of IDH mutation status in newly diagnosed FLT3-ITD+ mutated acute myeloid leukemia

  12. IDH1 gene mutations is a complex multi-layered process

  13. Patients with IDH1 mutation and low MCM6 expression exhibited the longest survival

  14. Isocitrate dehydrogenases mutated cases were significantly older but presented with similar rates of advanced-stage disease and sex distribution

  15. clinical prognostication in glioblastoma patients largely depends on classification of IDH mutant and wild type glioblastoma, and not on the presence of IDH1 rs11554137:C>T SNP in the tumor

  16. in intrahepatic cholangiocarcinoma, mutation correlates with a beneficial prognosis and inhibits tumor growth by suppressing Akt signaling

  17. The data show that mutant IDH1 reprogramming of the epigenome and transcriptome is dynamic.

  18. These findings argue against supply of either substrate being limiting for 2-HG production by a cytosolic IDH1 mutant and suggest that the retention of a WT allele in IDH1 mutant tumors is not due to a requirement for carbon or cofactor flux between WT and mutant IDH1.

  19. Our findings revealed that a IDH1(low)/Snail(high) molecular signature could serve as an independent biomarker for poor prognosis in breast cancer.

  20. The present review discusses the molecular basis of the sensitivity of IDH1/2-mutated cancers with respect to the function of mutated IDH1/2 in cellular processes and their interactions with novel IDH1/2-mutant inhibitors. Finally, lessons learned from IDH1/2 mutations for future clinical applications in IDH1/2 wild-type cancers are discussed.[ review]

Mouse (Murine) Isocitrate Dehydrogenase 1 (NADP+), Soluble (IDH1) interaction partners

  1. combined expression of Jak2V617F and mutant IDH1R132H or Idh2R140Q induces myeloproliferative neoplasm progression, alters stem/progenitor cell function, and impairs differentiation

  2. Vitamin C treatment induced an IDH1(R132H)-dependent reduction in cell proliferation.

  3. IDH1 expression regulates TCA cycle in glioma and affects glioma cell growth.GDH2 promotes growth of IDH1-expressing gliomas.

  4. Through the use of a conditional mutant mouse model that confers a less aggressive tumor phenotype, findings provide new insight into the effects of mutant Idh1 on a candidate cell of origin for glioma, mutant Idh1's role in disrupting the microenvironment from which gliomas arise, and mutant Idh1's effect on the course of glioma progression.

  5. IDH1 mutations caused down-regulation of leukocyte chemotaxis, resulting in repression of the tumor-associated immune system.

  6. Idh1(R132H) mutation in the major adult neurogenic stem cell niche causes a phenotype resembling gliomagenesis

  7. Mutant IDH1 downregulates the DNA damage (DD) sensor ATM by altering histone methylation, leading to impaired DNA repair, increased sensitivity to DD, and reduced HSC self-renewal, independent of TET2.

  8. Using whole RNA sequencing of bone marrow cells in iron-overloaded mice, it was observed that Idh1 and Aco1, enzymes involved in the TCA cycle, were elevated.

  9. data suggest that mutant IDH1 contributes to malignancy in the T-cell lineage and may alter the metabolic profile of malignant T cells

  10. The results suggest that Idh1 has a physiological function in protecting cells from oxidative stress by regulating the intracellular NADP(+)/NADPH ratio.

  11. These results support the translational potential of immunotherapeutic targeting of gliomas carrying IDH1 mutations R132H.

  12. MiR-181a regulates lipid metabolism via IDH1

  13. revealed a role for IDH1 in the synthesis/turnover of phospholipids in developing astrocytes and highlight the lipid alterations resulting from the loss of wild-type IDH1 activity.

  14. these data show that mutant IDH or d-2HG causes persistence of chondrocytes, giving rise to rests of growth-plate cells that persist in the bone as enchondromas.

  15. WA might exert its chemopreventive activity via inhibiting not only oncogenic activation, but also IDH1 inactivation.

  16. Brain-specific Idh1-KI mice show brain hemorrhage accompanied by high D2HG levels but decreased ROS

  17. Suggest that decreased IDPc expression renders melanocytes more vulnerable to oxidative stress, and IDPc plays an important antioxidant function in melanocytes.

  18. Absence of IDH1 mutations in low-grade gliomas (LGGs) identifies a novel entity of LGGs with distinctive location, infiltrative behavior, specific molecular alterations, and dismal outcome.

  19. a possible association between IDH mutations and trisomy 8 in myelodysplastic syndromes and acute myeloid leukemia.

  20. IDPc would be a major NADPH producer required for fat and cholesterol synthesis.

Cow (Bovine) Isocitrate Dehydrogenase 1 (NADP+), Soluble (IDH1) interaction partners

  1. Data suggest that the expression of cytosolic NADP+-dependent isocitrate dehydrogenase in bovine mammary epithelium is modulated by regulators of differentiation including extracellular matrix and lactogenic hormones as well as metabolic effectors.

Zebrafish Isocitrate Dehydrogenase 1 (NADP+), Soluble (IDH1) interaction partners

  1. generated a transgenic zebrafish model system for mutations in IDH1 that can be used for functional analysis and drug screening. Our model systems help understand the biology of IDH1 mutations and its role in tumor formation.

IDH1 Antigen Profile

Antigen Summary

Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. Each NADP(+)-dependent isozyme is a homodimer. The protein encoded by this gene is the NADP(+)-dependent isocitrate dehydrogenase found in the cytoplasm and peroxisomes. It contains the PTS-1 peroxisomal targeting signal sequence. The presence of this enzyme in peroxisomes suggests roles in the regeneration of NADPH for intraperoxisomal reductions, such as the conversion of 2, 4-dienoyl-CoAs to 3-enoyl-CoAs, as well as in peroxisomal reactions that consume 2-oxoglutarate, namely the alpha-hydroxylation of phytanic acid. The cytoplasmic enzyme serves a significant role in cytoplasmic NADPH production.

Gene names and symbols associated with IDH1

  • isocitrate dehydrogenase (NADP(+)) 1, cytosolic (IDH1) antibody
  • isocitrate dehydrogenase 1 (NADP+), soluble (Idh1) antibody
  • isocitrate dehydrogenase (NADP(+)) 1, cytosolic (Idh1) antibody
  • isocitrate dehydrogenase 1 (NADP+) L homeolog (idh1.L) antibody
  • isocitrate dehydrogenase 1 (NADP+), soluble (idh1) antibody
  • AI314845 antibody
  • AI788952 antibody
  • cb876 antibody
  • E030024J03Rik antibody
  • fm90e09 antibody
  • Id-1 antibody
  • IDCD antibody
  • IDH antibody
  • Idh-1 antibody
  • IDP antibody
  • Idpc antibody
  • im:7143416 antibody
  • NADP-CICDH antibody
  • PICD antibody
  • wu:fm90e09 antibody

Protein level used designations for IDH1

NADP(+)-specific ICDH , NADP-dependent isocitrate dehydrogenase, cytosolic , NADP-dependent isocitrate dehydrogenase, peroxisomal , isocitrate dehydrogenase [NADP] cytoplasmic , oxalosuccinate decarboxylase , IDH , IDP , cytosolic NADP-isocitrate dehydrogenase , isocitrate dehydrogenase 1 (NADP+), soluble , isocitrate dehydrogenase [NADP] cytoplasmic-like , Isocitrate dehydrogenase 1, soluble , isocitrate dehydrogenase 1

3417 Homo sapiens
443257 Ovis aries
751618 Felis catus
100414768 Callithrix jacchus
15926 Mus musculus
24479 Rattus norvegicus
494713 Xenopus laevis
281235 Bos taurus
100328559 Oryctolagus cuniculus
478889 Canis lupus familiaris
100006589 Danio rerio
100729107 Cavia porcellus
100066416 Equus caballus
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