Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
The product of GAPDH catalyzes an important energy-yielding step in carbohydrate metabolism, the reversible oxidative phosphorylation of glyceraldehyde-3-phosphate in the presence of inorganic phosphate and nicotinamide adenine dinucleotide (NAD). Additionally we are shipping GAPDH Antibodies (872) and GAPDH Proteins (71) and many more products for this protein.
Showing 10 out of 48 products:
Human GAPDH ELISA Kit for Sandwich ELISA - ABIN417410
Seipel, Marques, Bozzini, Meinken, Mueller, Pabst: Inactivation of the p53-KLF4-CEBPA Axis in Acute Myeloid Leukemia. in Clinical cancer research : an official journal of the American Association for Cancer Research 2016
Show all 2 Pubmed References
This suggests that RX624 might be useful as a drug against polyglutamine pathologies, and that is could be administered exogenously without affecting target cell physiology. This protective effect was validated by the similar effect of an anti-GAPDH specific antibody.
GAPDH can interact with proteins participating in DNA repair, such as APE1 (show APEX1 ELISA Kits), PARP1 (show PARP1 ELISA Kits), HMGB1 (show HMGB1 ELISA Kits), and HMGB2 (show HMGB2 ELISA Kits). In this review, the functions of GAPDH associated with DNA repair are discussed in detail.
Nitric oxide-induced GAPDH aggregation specifically induces mitochondrial dysfunction via permeability transition pore opening, leading to cell death.
GAPDH may act as a chaperone in heme transfer to downstream areas
NAD(+) inhibited both GAPDH aggregation and co-aggregation with GOSPEL, a hitherto undescribed effect of the coenzyme against the consequences of oxidative stress.
Monoclonal Antibodies DSHB-hGAPDH-2G7 and DSHB-hGAPDH-4B7 Against Human Glyceraldehyde-3-Phosphate Dehydrogenase.
the present study suggests that GAPDH plays an important role in cancer metastasis by affecting EMT (show ITK ELISA Kits) through regulation of Sp1 (show PSG1 ELISA Kits)-mediated SNAIL (show SNAI1 ELISA Kits) expression.
Knockdown of LAMP2A, a CMA-related protein, and TSG101 (show TSG101 ELISA Kits), an mA-related protein, significantly but only partially decreased the punctate accumulation of GAPDH-HT in AD293 cells and primary cultured rat cortical neurons.
In conclusion, the data show that two GAPDH binders could be therapeutically relevant in the treatment of injuries stemming from hard oxidative stress.
transient silencing of GAPDH reduces intracellular ROS (show ROS1 ELISA Kits) and facilitates increased autophagy, thereby reducing acute hypoxia and reoxygenation injury as well as the resulting apoptosis and necrosis.
GAPDH with CytOx could be the point of interest as it has already been shown that GAPDH protein damage results in a marked decrease in cellular ATP levels
present in, and accounts for, glycolysis and glutamate (show GRIN2A ELISA Kits) accumulation into synaptic vesicles
GAPDH phosphorylates the long intracellular loop of GABA(A) receptor alpha1 subunit at Ser (show SIGLEC1 ELISA Kits)-416 & Thr (show TRH ELISA Kits)-337. The neuronal membrane-attached GAPDH is a dual-purpose enzyme, a glycolytic dehydrogenase, & a receptor-associated kinase.
Results show that expression of GAPD increased during the late fattening stage of of hanwoo steers and it is involved in metabolic pathways such as glycolysis and the TCA cycle.
amino acid sequences were used to establish the 3D structures of the active site of glyceraldehyde-3-phosphate dehydrogenase and the phylogenetic relationships of the sardine and octopus enzymes
The expression level of GAPDH was upregulated to a greater extent than those for myogenin (show MYOG ELISA Kits) and myostatin 1 under restricted feeding.
These findings show that post-translational modification of GAPDH lysine residues regulates hepatic and systemic metabolism, revealing an unappreciated role for hepatic GAPDH in substrate selection and utilization.
These results suggest that GAPDH is an ancient, evolutionarily conserved receptor that plays a key role in the Plg (show PLG ELISA Kits)-dependent regulation of macrophage recruitment in the inflammatory response to microbial aggression, thus pitting prokaryotic GAPDH against mammalian GAPDH, with both involved in a conserved role of Plg (show PLG ELISA Kits) activation on the surface of their respective cells, to conflicting ends.
GAPDH-mediated expression regulation of sodium channel genes was associated with epilepsy and the anticonvulsant action of the ketogenic diet.
Exosomal GAPDH from Proximal Tubule Cells Regulate ENaC (show SCNN1A ELISA Kits) Activity
Data indicate that lactoferrin (show LTF ELISA Kits) uptake across duodenum by glyceraldehyde-3-phosphate dehydrogenase (GAPDH).
astrocytic production of D-serine is modulated by glycolytic activity via interactions between GAPDH and SRR (show SRR ELISA Kits).
Selective inhibition of the glycolytic pathway through GAPDH in chronic lymphocytic leukemia cells with nanoliposomal C6-ceramide could be an effective therapy for leukemia by targeting the Warburg effect.
glyceraldehyde-3-phosphate dehydrogenase plays a critical role in determining the superior functions of female bone marrow-derived mesenchymal stem cells in cell therapy against pulmonary arterial hypertension.
Data indicate that the HNO-nonsteroidal anti-inflammatory drugs (NSAIDs) prodrug inhibited cylcooxgenase-2 and glyceraldehyde 3-phosphate dehydrogenase activity and triggered significant sarcomere shortening on murine ventricular myocytes.
Gapdh is a moonlighting protein that functions as a glycolytic enzyme and a transferrin receptor.
The effect of metal ions on the activity of glyceraldehyde-3-phosphate dehydrogenase.
The structure-bound sperm-specific enzymes, GAPDH-S and pyruvate kinase(PK-S), appeared only late in spermatogenesis simultaneously with the development of the structures to which they are bound.
has been shown that the stage of aggregate growth follows the first-order kinetics and the experimentally measured rate constant of the first order corresponds to heat-induced structural reorganization of UV-irradiated GAPDH containing concealed damage.
Low micromolar levels of 3,4-dihydroxyphenylacetaldehyde caused extensive GAPDH aggregation and irreversibly inhibited enzyme activity.
The level of GAPDH-AP DNA adduct formation depends on oxidation of the protein SH-groups; disulfide bond reduction in GAPDH leads to the loss of its ability to form the adducts with AP DNA
The strength, selectivity, reversibility, and redox sensitivity of heme binding to GAPDH are consistent with it performing heme sensing or heme chaperone-like functions in cells.
Purified UCH-L1 (show UCHL1 ELISA Kits) and GAPDH were nitrated in vitro with peroxynitrite and the presence of nitrated proteins was confirmed by anti-3-nitrotyrosine Western blots.Subsequent validation with synthetic peptides was conducted for selected nitropeptides.
dissociation of alpha-crystallin and GAPDH
results strongly suggest that Tyr311 and Tyr317 nitration prohibits NAD(+) binding, leading to the loss of catalytic activity of GAPDH.
In the presence of alpha-crystallin or GroEL the kinetic of GAPDH aggregation is changed from the diffusion-limited cluster-cluster aggregation to the reaction-limited cluster-cluster aggregation.
The interactions described herein between the beta subunit (show POLG ELISA Kits) of PhK and GAPDH provide a possible mechanism for the direct linkage of glycogenolysis and glycolysis in skeletal muscle.
FKBP36 diminishes GAPDH activity by direct interaction and down-regulation of GAPDH
The product of this gene catalyzes an important energy-yielding step in carbohydrate metabolism, the reversible oxidative phosphorylation of glyceraldehyde-3-phosphate in the presence of inorganic phosphate and nicotinamide adenine dinucleotide (NAD). The enzyme exists as a tetramer of identical chains. Many pseudogenes similar to this locus are present in the human genome. Two transcript variants encoding different isoforms have been found for this gene.
aging-associated gene 9 protein
, peptidyl-cysteine S-nitrosylase GAPDH
, 38 kDa BFA-dependent ADP-ribosylation substrate
, G3-P dehydrogenase
, Glyceraldehyde-3-phosphate dehydrogenase1
, glyceraldehyde 3 phosphate dehydrogenase
, glyceraldehyde 3 phosphate dehydrogenase 1
, glyceraldehyde 3 phosphate dehydrogenase1
, glyceraldehyde-3-phosphate dehydrogenase
, glyceraldehyde phosphate dehydrogenase
, glyceraldehyde-3-phosphate dehydrogenase, type I
, glyceraldehyde-3-phosphate dehydrogenase-like