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  2. Polyclonal

GTX101245

DLD antibody

Cannot supply to this region.

SKU:
GTX101245
Additional Names:
dihydrolipoamide dehydrogenase , DLDD , DLDH , E3 , GCSL , LAD , PHE3
Application:
WB, IHC-P, IF, ICC
Concentration:
1 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Protein A Purified
Storage Conditions:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:
Genetex
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Buffer:
PBS, 20% Glycerol, 0.01% Thimerosal.
Immunogen:
Recombinant protein encompassing a sequence within the center region of human DLD. The exact sequence is proprietary.
Uniprot:
P09622
Synonyms:
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;OGDC-E3;PHE3
Extra Details:
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]
Shipping Conditions:
Blue Ice