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LCA5 anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement LCA5 dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN632308

Aperçu rapide pour LCA5 anticorps (N-Term) (ABIN632308)

Antigène

Voir toutes LCA5 Anticorps
LCA5 (Leber Congenital Amaurosis 5 (LCA5))

Reactivité

  • 25
  • 18
  • 17
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 25
Lapin

Clonalité

  • 25
Polyclonal

Conjugué

  • 7
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp LCA5 est non-conjugé

Application

  • 21
  • 13
  • 6
  • 3
  • 2
Western Blotting (WB)
  • Épitope

    • 6
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificité

    LCA5 antibody was raised against the N terminal of LCA5

    Purification

    Affinity purified

    Immunogène

    LCA5 antibody was raised using the N terminal of LCA5 corresponding to a region with amino acids FSLQKLKEISEARHLPERDDLAKKLVSAELKLDDTERRIKELSKNLELST
  • Indications d'application

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

    Commentaires

    LCA5 Blocking Peptide, (ABIN938457), is also available for use as a blocking control in assays to test for specificity of this LCA5 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of LCA5 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

    LCA5 (Leber Congenital Amaurosis 5 (LCA5))

    Autre désignation

    LCA5

    Sujet

    LCA5 is a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Mutations in this gene cause Leber congenital amaurosis type V. Alternative splicing results in two transcript variants.

    Poids moléculaire

    80 kDa (MW of target protein)
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