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DLD anticorps (Middle Region)

Cet anticorps Lapin Polyclonal détecte spécifiquement DLD dans WB. Il présente une réactivité envers Humain et Chien.
N° du produit ABIN631024

Aperçu rapide pour DLD anticorps (Middle Region) (ABIN631024)

Antigène

Voir toutes DLD Anticorps
DLD (Dihydrolipoamide Dehydrogenase (DLD))

Reactivité

  • 46
  • 28
  • 27
  • 7
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
Humain, Chien

Hôte

  • 53
  • 6
Lapin

Clonalité

  • 49
  • 10
Polyclonal

Conjugué

  • 37
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DLD est non-conjugé

Application

  • 54
  • 24
  • 23
  • 14
  • 13
  • 10
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 6
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region

    Specificité

    DLD antibody was raised against the middle region of DLD

    Purification

    Affinity purified

    Immunogène

    DLD antibody was raised using the middle region of DLD corresponding to a region with amino acids AGEMVNEAALALEYGASCEDIARVCHAHPTLSEAFREANLAASFGKSINF
  • Indications d'application

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

    Commentaires

    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

    Conseil sur la manipulation

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

    Stock

    4 °C/-20 °C

    Stockage commentaire

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

    DLD (Dihydrolipoamide Dehydrogenase (DLD))

    Autre désignation

    DLD

    Sujet

    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.

    Poids moléculaire

    56 kDa (MW of target protein)

    Pathways

    Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
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