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HFE anticorps

HFE Reactivité: Humain WB Hôte: Lapin Monoclonal unconjugated
N° du produit ABIN7267606
  • Antigène Voir toutes HFE Anticorps
    HFE (Hemochromatosis (HFE))
    Reactivité
    • 53
    • 8
    • 7
    • 5
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 48
    • 6
    Lapin
    Clonalité
    • 50
    • 4
    Monoclonal
    Conjugué
    • 26
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp HFE est non-conjugé
    Application
    • 41
    • 19
    • 14
    • 13
    • 13
    • 6
    • 5
    • 4
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB)
    Fonction
    HFE Rabbit mAb
     Réactivité croisée
    Humain
    Attributs du produit
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    A synthesized peptide derived from human HFE.
    Isotype
    IgG
    Top Product
    Discover our top product HFE Anticorps primaire
  • 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
    HFE (Hemochromatosis (HFE))
    Autre désignation
    HFE (HFE Produits)
    Synonymes
    anticorps HFE1, anticorps HH, anticorps HLA-H, anticorps MVCD7, anticorps TFQTL2, anticorps MR2, anticorps hemochromatosis, anticorps HFE, anticorps Hfe
    Sujet
    The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene. At least nine alternatively spliced variants have been described for this gene. Additional variants have been found but their full-length nature has not been determined.,HFE, HFE1, HH, HLA-H, MVCD7, TFQTL2, hemochromatosis,Signal Transduction,Endocrine & Metabolism,Neuroscience,Neurodegenerative Diseases Markers,Other Neurological disorders,Stem Cells,Hematopoietic Progenitors,Amyotrophic lateral sclerosis-ALS,HFE
    Poids moléculaire
    40kDa
    ID gène
    3077
    UniProt
    Q30201
    Pathways
    Transition Metal Ion Homeostasis, Regulation of Leukocyte Mediated Immunity, Positive Regulation of Immune Effector Process
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