Conjugation: FITC: Fluorescein Isothiocyanate
Description of Target: DLD 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.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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Immunogen: The immunogen is a synthetic peptide directed towards the middle region of human DLD
Key Reference: Wang,Y.C., (2008) J. Biomed. Sci. 15 (1), 37-46
Molecular Weight: 56kDa
Peptide Sequence: Synthetic peptide located within the following region:
AGEMVNEAALALEYGASCEDIARVCHAHPTLSEAFREANLAASFGKSINFProduct Format: Liquid. Purified antibody supplied in 1x PBS buffer.
Protein Name: Dihydrolipoyl dehydrogenase, mitochondrial
Protein Size: 509
Purification: Affinity Purified
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