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Periaxin Antikörper

Der Kaninchen Polyklonal Anti-Periaxin-Antikörper wurde für WB, ELISA und FACS validiert. Er ist geeignet, Periaxin in Proben von Maus, Human und Ratte zu detektieren.
Produktnummer ABIN5708499

Kurzübersicht für Periaxin Antikörper (ABIN5708499)

Target

Alle Periaxin (PRX) Antikörper anzeigen
Periaxin (PRX)

Reaktivität

Maus, Human, Ratte

Wirt

  • 23
  • 1
Kaninchen

Klonalität

  • 24
Polyklonal

Konjugat

  • 8
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Periaxin Antikörper ist unkonjugiert

Applikation

  • 22
  • 13
  • 13
  • 7
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Aufreinigung

    Antigen affinity purified

    Immunogen

    A recombinant human protein corresponding to amino acids M1-K91 was used as the immunogen for the Periaxin antibody.

    Isotyp

    IgG
  • Applikationshinweise

    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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    -20 °C

    Informationen zur Lagerung

    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.
  • Target

    Periaxin (PRX)

    Andere Bezeichnung

    Periaxin / PRX

    Hintergrund

    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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