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Periaxin anticorps

PRX Reactivité: Rat, Souris, Humain WB, ELISA, FACS Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5708499
  • Antigène Voir toutes Periaxin (PRX) Anticorps
    Periaxin (PRX)
    Reactivité
    Rat, Souris, Humain
    Hôte
    • 38
    Lapin
    Clonalité
    • 38
    Polyclonal
    Conjugué
    • 9
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Cet anticorp Periaxin est non-conjugé
    Application
    • 36
    • 26
    • 26
    • 10
    • 8
    • 6
    • 3
    • 2
    • 2
    • 2
    Western Blotting (WB), ELISA, Flow Cytometry (FACS)
    Purification
    Antigen affinity purified
    Immunogène
    A recombinant human protein corresponding to amino acids M1-K91 was used as the immunogen for the Periaxin antibody.
    Isotype
    IgG
    Top Product
    Discover our top product PRX Anticorps primaire
  • Indications d'application
    Optimal dilution of the Periaxin antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL,FACS: 1-3 μg/10^6 cells,Direct ELISA: 0.1-0.5 μg/mL
    Restrictions
    For Research Use only
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Stock
    -20 °C
    Stockage commentaire
    After reconstitution, the Periaxin antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Antigène
    Periaxin (PRX)
    Autre désignation
    Periaxin / PRX (PRX Produits)
    Synonymes
    anticorps xprx, anticorps MGC89167, anticorps CMT4F, anticorps L-Periaxin, anticorps periaxin, anticorps prx, anticorps PRX, anticorps Prx
    Sujet
    Periaxin is a protein that in humans is encoded by the PRX gene. This gene encodes a protein involved in peripheral nerve myelin upkeep. The encoded protein contains 2 PDZ domains which were named after PSD95 (post synaptic density protein), DlgA (Drosophila disc large tumor suppressor), and ZO1 (a mammalian tight junction protein). Two alternatively spliced transcript variants have been described for this gene which encode different protein isoforms and which are targeted differently in the Schwann cell. Mutations in this gene cause Charcot-Marie-Tooth neuoropathy, type 4F and Dejerine-Sottas neuropathy.
    UniProt
    Q9BXM0
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