DLD Polyclonal Antibody | E-AB-14947

DLD Polyclonal Antibody | E-AB-14947 | Gentaur UK, US & Europe Distribution

Type: Polyclonal Antibody

Synonyms: Dehydrogenase complex, E3 component, Diaphorase, Dihydrolipoamide dehydrogenase, Dihydrolipoyl dehydrogenase, Dihydrolipoyl dehydrogenase mitochondrial, dld, DLDD, DLDH, DLDH, E3, E3 branched chain aplha-keto acid, E3 component of pyruvate dehydrogenase, E3 component of pyruvate dehydrogenase complex 2 oxo glutarate complex branched chain keto acid dehydrogenase complex, GCSL, Glycine cleavage system L protein, Glycine cleavage system protein L, LAD, lipoamide dehydrogenase, Lipoamide reductase, Lipoyl dehydrogenase, mitochondrial, OTTHUMP00000206744, OTTHUMP00000206746, OTTHUMP00000206748, OTTHUMP00000206749, PHE 3, PHE3, Pyruvate dehydrogenase component E3

Application: IHC, ELISA

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Reserch Areas: Cancer, Metabolism, Signal Transduction

Background: This gene encodes a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In homodimeric form, the encoded protein functions as a dehydrogenase and is found in several multi-enzyme complexes that regulate energy metabolism. However, as a monomer, this protein can function as a protease. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. Alternative splicing results in multiple transcript variants.

Concentration: 0.6 mg/mL

Storage: Store at -20°C. Avoid freeze / thaw cycles.

Immunogen: Recombinant protein of human DLD

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Purification Method: Affinity purification

Dilution: IHC 1:50-1:200

Clone: N/A

Conjugation: Unconjugated

Molecular Weight(Calculated): N/A

Molecular Weight(Observed): N/A