DLD (Lipoamide Dehydrogenase) monoclonal Antibody | MB63021

DLD (Lipoamide Dehydrogenase) monoclonal Antibody | MB63021 | Gentaur UK, US & Europe Distribution

Host: Mouse

Reactivity: Human, Monkey, Mouse, Rat, Dog

Application: FC, IF, WB

Application Range: WB 1:500, IF 1:100, FLOW 1:100

Background: This gene encodes the L protein of the mitochondrial glycine cleavage system. The L protein, also named dihydrolipoamide dehydrogenase, is also a component of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. [provided by RefSeq, Jul 2008]

Storage & Stability: PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Specificity: dihydrolipoamide dehydrogenase

Molecular Weight: 50.1 kDa (Predicted)

Note: For research use only, not for use in diagnostic procedure.

Alternative Names: DLDD; DLDH; E3; GCSL; LAD; PHE3

Immunogen: Full length human recombinant protein of human DLD (NP_000099) produced in HEK293T cell.

Conjugate: Unconjugated

Modification: Unmodification

Purification & Purity: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)

Pathway: N/A