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Product Description
DLD (Lipoamide Dehydrogenase) monoclonal Antibody | MB63023 | Bioworld
Host: Mouse
Reactivity: Human, Monkey, Mouse, Rat, Dog
Application: FC, WB
Application Range: WB 1:500, 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
