catalog number :
MBS9317692
products type :
ELISA Kit
products full name :
Mouse NAD-dependent malic enzyme, mitochondrial, ME2 ELISA Kit
products short name :
[malic enzyme 2, NAD (+) -dependent, mitochondrial]
products name syn :
[Mouse NAD-dependent malic enzyme; mitochondrial (ME2) ELISA kit; ODS1; malate dehydrogenase; pyruvic-malic carboxylase; malic enzyme 2; NAD (+) -dependent; mitochondrial]
other names :
[NAD-dependent malic enzyme, mitochondrial; NAD-dependent malic enzyme, mitochondrial; NAD-dependent malic enzyme, mitochondrial; malic enzyme 2, NAD(+)-dependent, mitochondrial; Malic enzyme 2]
products gene name :
[ME2]
other gene names :
[Me2; Me2; NAD-ME; AW120568; D030040L20Rik; NAD-ME]
uniprot entry name :
MAOM_MOUSE
specificity :
No significant cross-reactivity or interference between this analyte and analogues is observed.
storage stability :
Store all reagents at 2-8 degree C
other info1 :
Samples: Body fluids, tissue homogenates, secretions or feces samples. Assay Type: Quantitative Sandwich. Detection Range: 0.625 ng/ml - 20 ng/ml. Sensitivity: 0.1 ng/ml.
other info2 :
Intra-assay Precision: Intra-assay CV (%) is less than 15%. Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100].
products description :
Background/Introduction: This Quantitative Sandwich ELISA kit is only for in vitro research use only, not for drug, household, therapeutic or diagnostic applications! This kit is intended to be used for determination the level of ME2 (hereafter termed "analyte") in undiluted original Mouse body fluids, tissue homogenates, secretions or feces samples. This kit is NOT suitable for assaying non-biological sources of substances.
ncbi acc num :
NP_663469.1
ncbi gb acc num :
NM_145494.2
ncbi mol weight :
65,799 Da
ncbi pathways :
Pyruvate Metabolism Pathway (83197); Pyruvate Metabolism Pathway (373); Gluconeogenesis I Pathway (142839)
uniprot summary :
ME2: 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. [provided by RefSeq, Dec 2009]. Protein type: EC 1.1.1.38; Carbohydrate Metabolism - pyruvate; Oxidoreductase; Mitochondrial. Cellular Component: intracellular membrane-bound organelle; mitochondrion. Molecular Function: malate dehydrogenase (decarboxylating) activity; malic enzyme activity; metal ion binding; oxidoreductase activity; NAD binding; catalytic activity; oxaloacetate decarboxylase activity. Biological Process: malate metabolic process; metabolic process
size4 :
10x96-Strip-Wells