DLD protein (His tag) (80R-1275)
Purified recombinant Human DLD protein
|Synonyms||E3 component of pyruvate dehydrogenase protein, Glycine cleavage system protein L protein, Dihydrolipoyl dehydrogenase mitochondrial protein, E3 component of pyruvate dehydrogenase complex 2 oxo glutarate complex branched chain keto acid dehydrogenase complex protein, GCSL protein, Dihydrolipoamide dehydrogenase protein, Glycine cleavage system L protein protein, Dihydrolipoyl dehydrogenase protein, DLDH protein, LAD protein, Dihydrolipoyl dehydrogenase protein, Lipoamide reductase protein, PHE 3 protein, mitochondrial Diaphorase protein, E3 protein, , DLD protein, Lipoyl dehydrogenase protein, PHE3 protein|
Coomassie Blue stained SDS-PAGE of DLD protein (His tag) (80R-1275)
Figure annotation denotes ug of protein loaded and % gel used.
|Residues||36-509 amino acids: MRGSHHHHHH GMASMTGGQQ MGRDLYDDDD KDRWGSMADQ PIDADVTVIG SGPGGYVAAI KAAQLGFKTV CIEKNETLGG TCLNVGCIPS KALLNNSHYY HMAHGKDFAS RGIEMSEVRL NLDKMMEQKS TAVKALTGGI AHLFKQNKVV HVNGYGKITG KNQVTATKAD GGTQVIDTKN ILIATGSEVT PFPGITIDED TIVSSTGALS LKKVPEKMVV IGAGVIGVEL GSVWQRLGAD VTAVEFLGHV GGVGIDMEIS KNFQRILQKQ GFKFKLNTKV TGATKKSDGK IDVSIEAASG GKAEVITCDV LLVCIGRRPF TKNLGLEELG IELDPRGRIP VNTRFQTKIP NIYAIGDVVA GPMLAHKAED EGIICVEGMA GGAVHIDYNC VPSVIYTHPE VAWVGKSEEQ LKEEGIEYKV GKFPFAANSR AKTNADTDGM VKILGQKSTD RVLGAHILGP GAGEMVNEAA LALEYGASCE DIARVCHAHP TLSEAFREAN LAASFGKSIN F|
|Purity||> 95% pure|
|Molecular Weight||54.4 kDa (511aa)|
|Form & Buffer||Supplied as a liquid in 20 mM Tris-HCl buffer, pH 8.0, containing 1mM DTT, 0.1M NaCl and 10% glycerol.|
Storage & Safety
|Storage||Store at 4 deg C for short term storage (1/2 weeks). Aliquot and store at -20 deg C or - 70 deg C for long term storage. Avoid repeated freeze/thaw cycles.|
|Biological Significance||DLD (Dihydrolipoamide dehydrogenase), also known as GCSL (glycine cleavage system L protein), is a component of the glycine cleavage system as well as of the alpha ketoacid dehydrogenase complexes. DLD is a flavin-dependent oxidoreductase and functions as a component of the alpha-keto acid dehydrogenase, the pyruvate dehydrogenase, the alpha-ketoglutarate dehydrogenase, the branched-chain alpha-keto acid dehydrogenase and as the L protein in the mitochondrial glycine cleavage system. Mutations in DLD protein can result in MSUD (maple syrup urine disease) and congenital infantile lactic acidosis. Recombinant human DLD protein, fused to His-tag at N-terminus, was expressed in E. coli and purified by using conventional chromatography techniques.|
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