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CCBE1 anticorps (AA 163-191)

L’anticorps Lapin Polyclonal anti-CCBE1 a été validé pour WB. Il convient pour détecter CCBE1 dans des échantillons de Humain.
N° du produit ABIN1537916

Aperçu rapide pour CCBE1 anticorps (AA 163-191) (ABIN1537916)

Antigène

Voir toutes CCBE1 Anticorps
CCBE1 (Collagen and Calcium Binding EGF Domains 1 (CCBE1))

Reactivité

  • 20
  • 7
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
Humain

Hôte

  • 19
  • 2
Lapin

Clonalité

  • 21
Polyclonal

Conjugué

  • 16
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp CCBE1 est non-conjugé

Application

  • 21
  • 10
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB37238
  • Épitope

    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 163-191

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This CCBE1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 163-191 amino acids from the Central region of human CCBE1.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    CCBE1 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Date de péremption

    6 months
  • Antigène

    CCBE1 (Collagen and Calcium Binding EGF Domains 1 (CCBE1))

    Autre désignation

    CCBE1

    Sujet

    This gene is thought to function in extracellular matrix remodeling and migration. It is predominantly expressed in the ovary, but down regulated in ovarian cancer cell lines and primary carcinomas, suggesting its role as a tumour suppressor. Mutations in this gene have been associated with Hennekam lymphangiectasia-lymphedema syndrome, a generalized lymphatic dysplasia in humans.

    Poids moléculaire

    44103

    ID gène

    147372

    NCBI Accession

    NP_597716

    UniProt

    Q6UXH8
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