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DLD antibody

This Rabbit Polyclonal antibody specifically detects DLD in WB, IHC, ELISA and IF. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN7113484

Quick Overview for DLD antibody (ABIN7113484)

Target

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

Reactivity

  • 46
  • 27
  • 27
  • 7
  • 5
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 53
  • 6
Rabbit

Clonality

  • 49
  • 10
Polyclonal

Conjugate

  • 37
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DLD antibody is un-conjugated

Application

  • 54
  • 23
  • 22
  • 13
  • 13
  • 10
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    dihydrolipoamide dehydrogenase

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,

    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

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

    DLD (Dihydrolipoamide Dehydrogenase (DLD))

    Alternative Name

    DLD

    Background

    Synonyms:GCSL, LAD, PHE3 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.

    Molecular Weight

    54 kDa

    Gene ID

    1738

    UniProt

    P09622

    Pathways

    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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