Rabbit anti-DLD Antibody
Catalog #
DLD
Human
,Mouse
IHC
,IP
,WB
Rabbit
Polyclonal
Whole IgG
Between 459 and 509
IgG
Unconjugated
Antigen Affinity Purified
Product Details
Mouse,
Human
Dog
Human
2 - 8 °C
1 year from date of receipt
Dihydrolipoamide dehydrogenase (DLD) is a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. DLD has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In homodimeric form, DLD functions as a dehydrogenase and is found in several multi-enzyme complexes that regulate energy metabolism. However, as a monomer, this protein can function as a protease. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency [taken from NCBI Entrez Gene (Gene ID: 1738)].
Alternate Names
diaphorase; Dihydrolipoamide dehydrogenase; dihydrolipoyl dehydrogenase, mitochondrial; DLDD; DLDH; E3; E3 component of pyruvate dehydrogenase complex, 2-oxo-glutarate complex, branched chain keto acid dehydrogenase complex; epididymis secretory sperm binding protein; GCSL; glycine cleavage system L protein; glycine cleavage system protein L; LAD; lipoamide dehydrogenase; lipoamide reductase; lipoyl dehydrogenase; PHE3
Applications