Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

Amyloid Antikörper (APC)

Reaktivität: Human ELISA, IHC, WB, IP, ICC, IF Wirt: Kaninchen Polyclonal APC
Produktnummer ABIN2486477
  • Target
    Amyloid
    Reaktivität
    Human
    Wirt
    • 19
    Kaninchen
    Klonalität
    • 19
    Polyklonal
    Konjugat
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    APC
    Applikation
    • 19
    • 19
    • 19
    • 19
    • 19
    • 19
    • 10
    ELISA, Immunohistochemistry (IHC), Western Blotting (WB), Immunoprecipitation (IP), Immunocytochemistry (ICC), Immunofluorescence (IF)
    Spezifität
    Recognizes all types of amyloid oligomers. Appears to recog a peptide backbone epitope common to amyloid oligomers, but not found in native proteins, amyloidogenic monomer or mature amyloid fibrils.
    Kreuzreaktivität
    Eukaryonten, Human, Maus, Ratte
    Aufreinigung
    Protein A Purified
    Immunogen
    Synthetic molecular mimic of soluble oligomers
  • Applikationshinweise
    • WB (1:200)
    • IP (1:200)
    • optimal dilutions for assays should be determined by the user.
    Kommentare

    A 1:200 dilution of ABIN2486477 was sufficient for detection of amyloid oligomers in 10 μg of mouse brain lysates by colorimetric immunoblot analysis using Goat anti-rabbit IgG:HRP as the secondary antibody.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    PBS, 50 % glycerol, 0.09 % sodium azide, Storage buffer may change when conjugated
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C
    Informationen zur Lagerung
    Conjugated antibodies should be stored at 4°C
  • Target
    Amyloid
    Synonyme
    amyloid beta precursor protein antikoerper, App antikoerper
    Hintergrund
    Amyloid monomeric proteins can sometimes 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 fibres (1, 2). These include the amyloid-β peptide plaques and tau neurofibrillary tangles in senile plaques of Alzheimer's symptomology, the deposition of α-synuclein in the Lewy bodies of Parkinson's disease, and accumulation of polyglutamine-containing aggregates in Huntington's disease (2, 3).
    Gen-ID
    8666
    NCBI Accession
    NM_000484
    UniProt
    P05067
Sie sind hier:
Kundenservice