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Amyloid Fibrils Antikörper

Der Kaninchen Polyklonal Anti--Antikörper wurde für WB, DB, ELISA und IHC validiert. Er ist geeignet, in Proben von Human, Maus und Ratte zu detektieren.
Produktnummer ABIN1731752

Kurzübersicht für Amyloid Fibrils Antikörper (ABIN1731752)

Target

Amyloid Fibrils

Reaktivität

Human, Maus, Ratte

Wirt

  • 5
Kaninchen

Klonalität

  • 5
Polyklonal

Konjugat

  • 5
Unkonjugiert

Applikation

  • 5
  • 4
  • 4
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Dot Blot (DB), ELISA, Immunohistochemistry (IHC)
  • Spezifität

    Reacts withepitopes common to many human amyloid fibrils and fibrillar oligomers but not prefibrillar oligomers or natively folded proteins. Predicted to recognize mouse and rat based on sequence homology.

    Aufreinigung

    Purified

    Immunogen

    Fibrils prepared from human Abeta42 peptide

    Isotyp

    IgG
  • Applikationshinweise

    Working dilution: Optimal dilutions should be determined by the end user.
    The following are guidelines only:
    WB1 -2 μg/mL DB0.5 - 1 μg/mL IHC1 -5 μg/mL ELISA1 - 10 μg/mL with amyloid fibril-containing samples on the solid phase.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5 mg/mL

    Buffer

    PBS pH 7.0, 50 % glycerol

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handhabung

    Dilute in PBS or medium which is identical to that used in the assay system.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    This product is stable for at least 1 year at -20°C. Freeze in multiple aliquots to avoid repeated freeze-thaw cycles.
  • Target

    Amyloid Fibrils

    Hintergrund

    Amyloid monomeric proteins can oligomerize into destructive amyloid fibrils. Amyloidogenic conformations of non-disease related proteins can be created by partial protein misfolding or denaturation. Many degenerative diseases are known to be related to the accumulation of misfolded proteins as amyloid fibers.
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