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DLD (Dihydrolipoyl Dehydrogenase, Mitochondrial, Dihydrolipoamide Dehydrogenase, Glycine Cleavage System L Protein, PHE3, LAD, GCSL)

Cat no: D7800-10A

DLD (Dihydrolipoyl Dehydrogenase, Mitochondrial, Dihydrolipoamide Dehydrogenase, Glycine Cleavage System L Protein, PHE3, LAD, GCSL)

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 acid dehydrogenase complex. Mutations in DLD have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency.\n\nApplications:\nSuitable for use in Western Blot and Immunohistochemistry. Other applications have not been tested. \n\nRecommended Dilutions: \nWestern Blot: 1:1000-1:10,000 \nImmunohistochemistry: 1:100-1:250\nOptimal dilutions to be determined by the researcher. \n\nStorage and Stability:\nMay be stored at 4 degrees C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degrees C. Aliquots are stable for 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.\n\nManufactured incorporating RabMAb(R) technology under Epitomics US patents, No 5,675,063 and 7,429,487, owned by Abcam.

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SPECIFICATIONS

Catalog Number

D7800-10A

Size

100ul

Applications

IHC, WB

Hosts

Rabbit

Reactivities

Hum, Mouse

Form

Supplied as a liquid in PBS, pH 7.2, 0.05% BSA, 0.01% sodium azide, 50% glycerol.

P Type

Mab

Purity

Supernatant

Additional Info

Recognizes human DLD. Species crossreactivity: Mouse.

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