DLD Antibody

ProSci
Product Code: PSI-27-169
Product Group: Primary Antibodies
Supplier: ProSci
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PSI-27-169-100ul100ul£662.00
Quantity:
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Overview

Host Type: Rabbit
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species:
  • Canine (dog)
  • Human
Applications:
  • Enzyme-Linked Immunosorbent Assay (ELISA)
  • Western Blot (WB)
Storage:
For short periods of storage (days) store at 4˚C. For longer periods of storage, store DLD antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles.

Images

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Antibody used in WB on Human Jurkat 0.2-1 ug/ml.
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3 / 5
Antibody used in WB on Human Hela at 1 ug/ml.
4 / 5
Antibody used in WB on Hum. Adult Placenta at 1 ug/ml.
5 / 5
Antibody used in WB on Human MCF7 at 1 ug/ml.

Antibody used in WB on Human Jurkat 0.2-1 ug/ml.
Antibody used in WB on Human Hela at 1 ug/ml.
Antibody used in WB on Hum. Adult Placenta at 1 ug/ml.
Antibody used in WB on Human MCF7 at 1 ug/ml.

Further Information

Additional Names:
DLD, DLDH, E3, GCSL, LAD, PHE3, DLDD
Application Note:
DLD antibody can be used for detection of DLD by ELISA at 1:62500. DLD antibody can be used for detection of DLD by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Background:
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 acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency.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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Background References:
  • Wang, Y.C., (2008) J. Biomed. Sci. 15 (1), 37-46.
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Conjugate:
Unconjugated
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human DLD.
NCBI Gene ID #:
1738
NCBI Official Name:
dihydrolipoamide dehydrogenase
NCBI Official Symbol:
DLD
NCBI Organism:
Homo sapiens
Physical State:
Liquid
PREDICTED MOLECULAR WEIGHT:
56 kDa
Protein Accession #:
NP_000099
Protein GI Number:
91199540
Purification:
Antibody is purified by peptide affinity chromatography method.
Swissprot #:
B2R5X0
User NOte:
Optimal dilutions for each application to be determined by the researcher.