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APOB anticorps

Cet anticorps Lapin Monoclonal détecte spécifiquement APOB dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN7265635

Aperçu rapide pour APOB anticorps (ABIN7265635)

Antigène

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

Reactivité

  • 106
  • 27
  • 27
  • 7
  • 3
Humain

Hôte

  • 70
  • 49
  • 14
  • 2
  • 2
Lapin

Clonalité

  • 85
  • 50
Monoclonal

Conjugué

  • 61
  • 23
  • 17
  • 7
  • 6
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp APOB est non-conjugé

Application

  • 78
  • 48
  • 43
  • 32
  • 23
  • 17
  • 10
  • 10
  • 7
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Fonction

    ApoB Rabbit mAb

     Réactivité croisée

    Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human ApoB

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • 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. [provided by RefSeq, Jul 2008],FLDB, LDLCQ4, apoB-100, apoB-48,Cancer,Cardiovascular,Cardiovascular diseases,Cardiovascular diseases_Heart disease,Endocrine & Metabolism,Heart,Lipid Metabolism,Lipid Metabolism_Cholesterol Metabolism,Lipids,Lipids_Lipoproteins/Apolipoproteins,Signal Transduction,APOB

    Poids moléculaire

    515kDa

    ID gène

    338

    UniProt

    P04114

    Pathways

    Lipid Metabolism
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