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PCDH15 anticorps (N-Term)

Cet anticorps anti-PCDH15 est un anticorps Lapin Polyclonal détectant PCDH15 dans WB. Adapté pour Humain, Souris et Rat.
N° du produit ABIN635568

Aperçu rapide pour PCDH15 anticorps (N-Term) (ABIN635568)

Antigène

Voir toutes PCDH15 Anticorps
PCDH15 (Protocadherin-15 (PCDH15))

Reactivité

  • 15
  • 7
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 12
  • 3
  • 3
Lapin

Clonalité

  • 15
  • 3
Polyclonal

Conjugué

  • 18
Cet anticorp PCDH15 est non-conjugé

Application

  • 15
  • 10
  • 6
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificité

    PCDH15 antibody was raised against the N terminal of PCDH15

    Purification

    Affinity purified

    Immunogène

    PCDH15 antibody was raised using the N terminal of PCDH15 corresponding to a region with amino acids HSIVVQVQCINKKVGTIIYHEVRIVVRDRNDNSPTFKHESYYATVNELTP
  • Indications d'application

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

    Commentaires

    PCDH15 Blocking Peptide, (ABIN939239), is also available for use as a blocking control in assays to test for specificity of this PCDH15 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of PCDH15 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

    PCDH15 (Protocadherin-15 (PCDH15))

    Autre désignation

    PCDH15

    Sujet

    PCDH15 is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. PCDH15 consists of a signal peptide, 11 extracellular calcium-binding domains, a transmembrane domain and a unique cytoplasmic domain. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene have been associated with hearing loss, which is consistent with its location at the Usher syndrome type 1F (USH1F) critical region on chromosome 10.

    Poids moléculaire

    80 kDa (MW of target protein)

    Pathways

    Sensory Perception of Sound
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