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ERCC5 anticorps (N-Term)

Cet anticorps anti-ERCC5 est un anticorps Lapin Polyclonal détectant ERCC5 dans WB. Adapté pour Humain, Souris et Rat.
N° du produit ABIN631899

Aperçu rapide pour ERCC5 anticorps (N-Term) (ABIN631899)

Antigène

Voir toutes ERCC5 Anticorps
ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))

Reactivité

  • 41
  • 12
  • 11
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 36
  • 5
Lapin

Clonalité

  • 37
  • 4
Polyclonal

Conjugué

  • 29
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp ERCC5 est non-conjugé

Application

  • 30
  • 14
  • 9
  • 6
  • 6
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 8
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificité

    ERCC5 antibody was raised against the N terminal of ERCC5

    Purification

    Affinity purified

    Immunogène

    ERCC5 antibody was raised using the N terminal of ERCC5 corresponding to a region with amino acids NPQAIDIESEDFSSLPPEVKHEILTDMKEFTKRRRTLFEAMPEESDDFSQ
  • Indications d'application

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

    Commentaires

    ERCC5 Blocking Peptide, (ABIN5613393), is also available for use as a blocking control in assays to test for specificity of this ERCC5 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ERCC5 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

    ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))

    Autre désignation

    ERCC5

    Sujet

    Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage.

    Poids moléculaire

    133 kDa (MW of target protein)

    Pathways

    Réparation de l'ADN
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