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CCDC115 anticorps (AA 1-180)

L’anticorps anti-CCDC115 Polyclonal Lapin est utilisé pour la détection de CCDC115 dans des échantillons de Humain. Il a été validé pour WB, ELISA, IF, IHC (p) et FACS.
N° du produit ABIN7868265
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour CCDC115 anticorps (AA 1-180) (ABIN7868265)

Antigène

Voir toutes CCDC115 Anticorps
CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))

Reactivité

  • 10
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 6
  • 4
Lapin

Clonalité

  • 8
  • 2
Polyclonal

Conjugué

  • 10
Cet anticorp CCDC115 est non-conjugé

Application

  • 10
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Épitope

    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-180

    Fonction

    CCDC115 Antibody

    Purification

    Antigen affinity purified

    Immunogène

    Recombinant human protein (amino acids M1-A180) was used as the immunogen for the CCDC115 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the CCDC115 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the CCDC115 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))

    Autre désignation

    CCDC115

    Sujet

    Coiled-coil domain containing 115 is a protein that in humans is encoded by the CCDC115 gene. The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans.

    UniProt

    Q96NT0
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