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Amyloid Oligomers antibody

Reactivity: Human, Mouse, Rat, Eukaryotes WB, IP, DB, IF, EIA, IHC (fro) Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN950404
  • Target
    Amyloid Oligomers
    Reactivity
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat, Eukaryotes
    Host
    • 4
    Rabbit
    Clonality
    • 4
    Polyclonal
    Conjugate
    • 4
    Un-conjugated
    Application
    • 4
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP), Dot Blot (DB), Immunofluorescence (IF), Enzyme Immunoassay (EIA), Immunohistochemistry (Frozen Sections) (IHC (fro))
    Specificity
    Recognizes all types of Amyloid oligomers. Appears to recognize a peptide backbone epitope that is common to Amyloid oligomers, but is not found in native proteins, amyloidogenic monomer or mature amyloid fibrils.
    Cross-Reactivity (Details)
    Species reactivity (tested):Human, Eukaryotes, Rat and Mouse.
    Purification
    Protein A Chromatography
    Immunogen
    Synthetic molecular mimic of soluble oligomers.
    Isotype
    IgG
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    PBS, 0.09 % Sodium Azide, 50 % Glycerol
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handling Advice
    Avoid repeated freezing and thawing.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target
    Amyloid Oligomers
    Background
    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).Synonyms: A11, Amyloid Oligomer AlphaBeta, amyloid, oligomers
    Gene ID
    351
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