DLD antibody
Quick Overview for DLD antibody (ABIN2854985)
Target
See all DLD AntibodiesReactivity
Host
Clonality
Conjugate
Application
Grade
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Cross-Reactivity
- Human, Mouse, Rat
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Characteristics
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Rabbit Polyclonal antibody to DLD (dihydrolipoamide dehydrogenase)
DLD antibody -
Purification
- Affinity purified by Protein A.
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Immunogen
- Recombinant protein encompassing a sequence within the center region of human DLD. The exact sequence is proprietary.
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Isotype
- IgG
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Application Notes
- WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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Comment
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Positive Control: Mouse brain , 293T , PC-12 , Rat2 , HeLa
Validation: KO/KD
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- 1XPBS ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
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Preservative
- Thimerosal (Merthiolate)
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Precaution of Use
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- 4 °C,-20 °C
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Storage Comment
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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: "Dihydrolipoamide dehydrogenase regulates cystine deprivation-induced ferroptosis in head and neck cancer." in: Redox biology, Vol. 30, pp. 101418, (2020) (PubMed).
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: "Dihydrolipoamide dehydrogenase regulates cystine deprivation-induced ferroptosis in head and neck cancer." in: Redox biology, Vol. 30, pp. 101418, (2020) (PubMed).
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- DLD (Dihydrolipoamide Dehydrogenase (DLD))
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Alternative Name
- dihydrolipoamide dehydrogenase
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Background
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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.
Cellular Localization: Mitochondrion matrix -
Molecular Weight
- 54 kDa
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Gene ID
- 1738
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UniProt
- P09622
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Pathways
- Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
Target
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