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DLD antibody

The Rabbit Polyclonal anti-DLD antibody is suitable to detect DLD in samples from Human, Mouse and Rat. It has been validated for IHC and ELISA.
Catalog No. ABIN7241168
$538.80
Plus shipping costs $50.00
Shipping to: United States
Delivery in 11 to 15 Business Days

Quick Overview for DLD antibody (ABIN7241168)

Target

See all DLD Antibodies
DLD (Dihydrolipoamide Dehydrogenase (DLD))

Reactivity

  • 56
  • 37
  • 36
  • 7
  • 5
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 64
  • 5
Rabbit

Clonality

  • 50
  • 19
Polyclonal

Conjugate

  • 38
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DLD antibody is un-conjugated

Application

  • 64
  • 31
  • 23
  • 22
  • 21
  • 9
  • 6
  • 4
  • 4
  • 2
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human DLD

    Isotype

    IgG
  • Application Notes

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.6 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    DLD (Dihydrolipoamide Dehydrogenase (DLD))

    Alternative Name

    DLD

    Background

    This gene encodes a member of the class-I pyridine nucleotide-disulfide oxidoreductase family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In homodimeric form, the encoded protein functions as a dehydrogenase and is found in several multi-enzyme complexes that regulate energy metabolism. However, as a monomer, this protein can function as a protease. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. Alternative splicing results in multiple transcript variants.

    UniProt

    P09622

    Pathways

    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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