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Purification and characterization of the plastid-localized NAD-dependent malate dehydrogenase from Arabidopsis thaliana
The critical role of plastidial NAD-specific MDH isoform in Arabidopsis (Arabidopsis thaliana) plants, is reported.
Arabidopsis thaliana mutants lacking the NADP-malate dehydrogenase have lost the reversible inactivation of catalase (显示 CAT 抗体) activity and the increase in H2O2 levels when exposed to high light.
plastid-localized NAD-dependent malate dehydrogenase is crucial for energy homeostasis in developing Arabidopsis thaliana seeds
mMDH (显示 MDH2 抗体) has a role in maximizing photorespiratory rate.
The chromosome 18q21 deletion in nearly one third of pancreatic adenocarcinomas eliminates not only the tumor suppressor SMAD4 (显示 SMAD4 抗体), but also neighboring genes with important cellular roles, such as ME2 (显示 CELSR1 抗体)
deletion of malic enzyme 2 (显示 NAD-ME 抗体) confers collateral lethality in pancreatic cancer
ME1 (显示 ME1 抗体)/ME2 (显示 CELSR1 抗体) expression phenotype may have a potential to be a valuable marker for sebaceous differentiation in sebaceous lesions.
Data indicate that malic enzyme 2 (显示 NAD-ME 抗体) knockdown impacts phosphatidylinositol 3-kinases/proto-oncogene (显示 RAB1A 抗体) protein akt (显示 AKT1 抗体) (PI3K (显示 PIK3CA 抗体)/AKT (显示 AKT1 抗体)) signaling.
ME2 (显示 CELSR1 抗体) might be an important factor in melanoma progression and a novel biomarker of invasion.
Three SNP alleles in BRD2 (显示 BRD2 抗体), Cx-36 (显示 GJD2 抗体), and ME2 (显示 CELSR1 抗体) and microdeletions in 15q13.3, 15q11.2, and 16p13.11 also contribute risk to juvenile myclonic epilepsy.
p53 (显示 TP53 抗体) represses the expression of the tricarboxylic-acid-cycle-associated malic enzymes ME1 (显示 ME1 抗体) and ME2 (显示 CELSR1 抗体) in human and mouse cells
Depletion of malic enzyme 2 (显示 NAD-ME 抗体) induced erythroid differentiation in human erythroleukemia cells.
An ME2-centered nine-SNP haplotype, when present homozygously, increases the risk for IGE (odds ratio 6.1; 95% confidence interval 2.9-12.7) compared with any other genotype
Schizophrenic subjects are identified with mitochondrial genes involved in oxidative metabolism as showing consistently decreased expression, including ME2 (显示 CELSR1 抗体).
This gene encodes a mitochondrial NAD-dependent malic enzyme, a homotetrameric protein, that catalyzes the oxidative decarboxylation of malate to pyruvate. It had previously been weakly linked to a syndrome known as Friedreich ataxia that has since been shown to be the result of mutation in a completely different gene. Certain single-nucleotide polymorphism haplotypes of this gene have been shown to increase the risk for idiopathic generalized epilepsy. Alternatively spliced transcript variants encoding different isoforms found for this gene.
, malic DH
, malic enzyme b
, oxidoreductase, putative
, malate dehydrogenase
, NAD-dependent malic enzyme, mitochondrial
, pyruvic-malic carboxylase