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HMBS anticorps

HMBS Reactivité: Humain, Souris, Rat WB, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7246280
  • Antigène Voir toutes HMBS Anticorps
    HMBS (Hydroxymethylbilane Synthase (HMBS))
    Reactivité
    • 61
    • 35
    • 35
    • 5
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 55
    • 5
    • 1
    Lapin
    Clonalité
    • 48
    • 13
    Polyclonal
    Conjugué
    • 26
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp HMBS est non-conjugé
    Application
    • 39
    • 13
    • 10
    • 8
    • 7
    • 5
    • 4
    • 4
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human HMBS
    Isotype
    IgG
    Top Product
    Discover our top product HMBS Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.08 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    HMBS (Hydroxymethylbilane Synthase (HMBS))
    Autre désignation
    HMBS (HMBS Produits)
    Sujet
    This gene encodes a member of the hydroxymethylbilane synthase superfamily. The encoded protein is the third enzyme of the heme biosynthetic pathway and catalyzes the head to tail condensation of four porphobilinogen molecules into the linear hydroxymethylbilane. Mutations in this gene are associated with the autosomal dominant disease acute intermittent porphyria. Alternatively spliced transcript variants encoding different isoforms have been described.
    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 39 kDa

    UniProt
    P08397
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