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DLD antibody (Middle Region)

This Rabbit Polyclonal antibody specifically detects DLD in WB. It exhibits reactivity toward Human and Dog.
Catalog No. ABIN631024

Quick Overview for DLD antibody (Middle Region) (ABIN631024)

Target

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

Reactivity

  • 50
  • 30
  • 29
  • 7
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Human, Dog

Host

  • 58
  • 7
Rabbit

Clonality

  • 54
  • 11
Polyclonal

Conjugate

  • 43
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DLD antibody is un-conjugated

Application

  • 60
  • 29
  • 23
  • 18
  • 16
  • 13
  • 7
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region

    Specificity

    DLD antibody was raised against the middle region of DLD

    Purification

    Affinity purified

    Immunogen

    DLD antibody was raised using the middle region of DLD corresponding to a region with amino acids AGEMVNEAALALEYGASCEDIARVCHAHPTLSEAFREANLAASFGKSINF
  • Application Notes

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    DLD Blocking Peptide, , is also available for use as a blocking control in assays to test for specificity of this DLD antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of DLD antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    DLD (Dihydrolipoamide Dehydrogenase (DLD))

    Alternative Name

    DLD

    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.

    Molecular Weight

    56 kDa (MW of target protein)

    Pathways

    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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