Product Name :DLD (Lipoamide Dehydrogenase) mouse monoclonal antibody (KU)
Reactivity :Human, Dog, Rat, Monkey, Mouse
Application_all :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]
Product :1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2
Purification&Purity :The antibody was affinity-purified from mouse ascites fluids or tissue culture supernatant by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Storage&Stability :Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
Note :For research use only, not for use in diagnostic procedure.
Alternative Name :DLDD; DLDH; E3; GCSL; LAD; PHE3
Immunogen :Full length human recombinant protein of human DLD(NP_000099) produced in HEK293T cell.
Modification :Unmodification
