Rat Mdh1 ELISA Kit (V2LY-0626-LY2419)

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Tested Data
Request for COA
Datasheet Target References Q & As Review & reward Protocols Associated Products

Basic Information

Sensitivity
1.355 mU/mL
Detection Range
3-900 mU/mL
Sample Type
Serum, Plasma, cell culture supernates
Specificity
Rat
Assay Type
Sandwich
Reactivity
Rat
Assay Time
1.5 h
Molecule Mass
36.5 kDa
Components
  • Pre-coated ELISA Plate: 12 wells * 8 detachable strips
  • Standard solution: 0.5ml x1
  • Standard diluent: 3ml x1
  • Streptavidin-HRP: 6ml x1
  • Stop solution: 6ml x1
  • Substrate solution A: 6ml x1
  • Substrate solution B: 6ml x1
  • Wash buffer concentrate (25x): 20ml x1
  • Biotinylated antibody: 1ml x1

Formulations & Storage [For reference only, actual COA shall prevail!]

Storage
Store at 2-8°C
More Infomation

Target

Full Name
MDH1
Function
Catalyzes the reduction of aromatic alpha-keto acids in the presence of NADH (PubMed:3052244).

Plays essential roles in the malate-aspartate shuttle and the tricarboxylic acid cycle, important in mitochondrial NADH supply for oxidative phosphorylation (PubMed:31538237).
Biological Process
Malate metabolic process Source: GO_Central
NADH metabolic process Source: GO_Central
Oxaloacetate metabolic process Source: GO_Central
Tricarboxylic acid cycle Source: GO_Central
Cellular Location
Cytoplasm
Involvement in disease
Developmental and epileptic encephalopathy 88 (DEE88):
A form of epileptic encephalopathy, a heterogeneous group of early-onset epilepsies characterized by refractory seizures, neurodevelopmental impairment, and poor prognosis. Development is normal prior to seizure onset, after which cognitive and motor delays become apparent. DEE88 is an autosomal recessive severe form characterized by global developmental delay, epilepsy, and progressive microcephaly.
PTM
ISGylated.
Acetylation at Lys-118 dramatically enhances enzymatic activity and promotes adipogenic differentiation.

Kwon, H. J., Hahn, K. R., Kang, M. S., Choi, J. H., Moon, S. M., Yoon, Y. S., ... & Kim, D. W. (2023). Tat-malate dehydrogenase fusion protein protects neurons from oxidative and ischemic damage by reduction of reactive oxygen species and modulation of glutathione redox system. Scientific Reports, 13(1), 5653.

Thomas, M. J., Cassidy, E. R., Robinson, D. S., & Walstrom, K. M. (2022). Kinetic characterization and thermostability of C. elegans cytoplasmic and mitochondrial malate dehydrogenases. Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics, 1870(1), 140722.

Zhu, Q., Zhou, H., Wu, L., Lai, Z., Geng, D., Yang, W., ... & Yi, W. (2022). O-GlcNAcylation promotes pancreatic tumor growth by regulating malate dehydrogenase 1. Nature chemical biology, 18(10), 1087-1095.

Imran, M., Munir, M. Z., Ialhi, S., Abbas, F., Younus, M., Ahmad, S., ... & Shafiq, S. (2022). Identification and Characterization of Malate Dehydrogenases in Tomato (Solanum lycopersicum L.). International Journal of Molecular Sciences, 23(17), 10028.

McCue, W. M., & Finzel, B. C. (2021). Structural characterization of the human cytosolic malate dehydrogenase I. ACS omega, 7(1), 207-214.

Gu, H., Chen, C., Hao, X., Su, N., Huang, D., Zou, Y., ... & Zheng, J. (2020). MDH1-mediated malate-aspartate NADH shuttle maintains the activity levels of fetal liver hematopoietic stem cells. Blood, The Journal of the American Society of Hematology, 136(5), 553-571.

Nan, N., Wang, J., Shi, Y., Qian, Y., Jiang, L., Huang, S., ... & Xu, Z. Y. (2020). Rice plastidial NAD‐dependent malate dehydrogenase 1 negatively regulates salt stress response by reducing the vitamin B6 content. Plant Biotechnology Journal, 18(1), 172-184.

Jin, J., Huang, S., & Pan, J. (2019). A Novel Role for Malate Dehydrogenase 1 in Acute Myeloid Leukemia Progression. Blood, 134, 5048.

Broeks, M. H., Shamseldin, H. E., Alhashem, A., Hashem, M., Abdulwahab, F., Alshedi, T., ... & Alkuraya, F. S. (2019). MDH1 deficiency is a metabolic disorder of the malate–aspartate shuttle associated with early onset severe encephalopathy. Human genetics, 138, 1247-1257.

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For research use only. Not intended for any clinical use.

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