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APOB anticorps

Cet anticorps Souris Monoclonal détecte spécifiquement APOB dans WB, IHC, ELISA et FACS. Il présente une réactivité envers Humain.
N° du produit ABIN865414
659,62 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 10 à 13 jours ouvrables

Aperçu rapide pour APOB anticorps (ABIN865414)

Antigène

Voir toutes APOB Anticorps
APOB (Apolipoprotein B (APOB))

Reactivité

  • 116
  • 27
  • 26
  • 6
  • 2
Humain

Hôte

  • 80
  • 47
  • 14
  • 2
  • 2
Souris

Clonalité

  • 84
  • 60
Monoclonal

Conjugué

  • 62
  • 24
  • 15
  • 7
  • 6
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp APOB est non-conjugé

Application

  • 86
  • 46
  • 42
  • 31
  • 30
  • 19
  • 17
  • 9
  • 7
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Flow Cytometry (FACS)

Clone

6G6
  • Purification

    Ascitic fluid

    Immunogène

    Purified recombinant fragment of human ApoB expressed in E. Coli.

    Isotype

    IgG1
  • Indications d'application

    WB: 1/500 - 1/2000, IHC: 1/200 - 1/1000, FC: 1/200 - 1/400 ELISA: Propose dilution 1/10000.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    100g/100l

    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
  • Antigène

    APOB (Apolipoprotein B (APOB))

    Autre désignation

    ApoB

    Sujet

    This gene product is the main apolipoprotein of chylomicrons and low density lipoproteins. It occurs in plasma as two main isoforms, apoB-48 and apoB-100: the former is synthesized exclusively in the gut and the latter in the liver. The intestinal and the hepatic forms of apoB are encoded by a single gene from a single, very long mRNA. The two isoforms share a common N-terminal sequence. The shorter apoB-48 protein is produced after RNA editing of the apoB-100 transcript at residue 2180 (CAA->UAA), resulting in the creation of a stop codon, and early translation termination. Mutations in this gene or its regulatory region cause hypobetalipoproteinemia, normotriglyceridemic hypobetalipoproteinemia, and hypercholesterolemia due to ligand-defective apoB, diseases affecting plasma cholesterol and apoB levels. Synonyms: FLDB, LDLCQ4

    Poids moléculaire

    516kDa

    ID gène

    338

    Pathways

    Lipid Metabolism
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