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Mouse Dihydrolipoyl dehydrogenase (DLD) ELISA Kit

Cat no: KTE71261

Mouse Dihydrolipoyl dehydrogenase (DLD) ELISA Kit

The dihydrolipoate, still bound to a lysine residue of the complex, then migrates to the dihydrolipoyl dehydrogenase (E3) active site where it undergoes a flavin-mediated oxidation, identical in chemistry to disulfide isomerase. First, FAD oxidizes dihydrolipoate back to its lipoate resting state, producing FADH2.\nDihydrolipoamide dehydrogenase is 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.

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SPECIFICATIONS

Catalog Number

KTE71261

Size

48T, 96T, 96T*5, 96T*50

Applications

ELISA

Reactivities

Mouse

Gene Id

13382

Accession

O08749

Additional Info

Mouse Dihydrolipoyl dehydrogenase (DLD) ELISA Kit has high sensitivity and excellent specificity for detection of Mouse DLD. No significant cross-reactivity or interference between Mouse DLD and analogues was observed.

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