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TMC8 anticorps (N-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement TMC8 dans WB. Il présente une réactivité avec des échantillons de Humain.
N° du produit ABIN632629
1.309,82 €
Plus frais de livraison 40,00 € et TVA
100 μL
Destination: France
Envoi sous 13 à 17 jours ouvrables

Aperçu rapide pour TMC8 anticorps (N-Term) (ABIN632629)

Antigène

Voir toutes TMC8 Anticorps
TMC8 (Transmembrane Channel-Like 8 (TMC8))

Reactivité

  • 33
  • 9
  • 9
Humain

Hôte

  • 33
Lapin

Clonalité

  • 33
Polyclonal

Conjugué

  • 14
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TMC8 est non-conjugé

Application

  • 32
  • 16
  • 13
  • 13
  • 5
  • 5
  • 4
  • 3
  • 2
  • 2
Western Blotting (WB)
  • Épitope

    • 15
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Specificité

    TMC8 antibody was raised against the N terminal of TMC8

    Purification

    Affinity purified

    Immunogène

    TMC8 antibody was raised using the N terminal of TMC8 corresponding to a region with amino acids PGPTLNLTLQCPGSRQSPPGVLRFHNQLWHVLTGRAFTNTYLFYGAYRVG
  • Indications d'application

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

    Commentaires

    TMC8 Blocking Peptide, (ABIN5616647), is also available for use as a blocking control in assays to test for specificity of this TMC8 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of TMC8 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

    TMC8 (Transmembrane Channel-Like 8 (TMC8))

    Autre désignation

    TMC8

    Sujet

    Epidermodysplasia verruciformis (EV) is an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin. EV is caused by mutations in either of two adjacent genes located on chromosome 17q25.3. Both of these genes encode integral membrane proteins that localize to the endoplasmic reticulum and are predicted to form transmembrane channels.

    Poids moléculaire

    82 kDa (MW of target protein)
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