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Amyloid Fibrils anticorps

Cet anticorps anti- est un anticorps Lapin Polyclonal détectant dans WB, DB, IP, EIA, IHC (fro) et IF. Adapté pour Humain. Ce Primary Antibody a été cité dans 3+ publications.
N° du produit ABIN950406

Aperçu rapide pour Amyloid Fibrils anticorps (ABIN950406)

Antigène

Amyloid Fibrils

Reactivité

  • 5
  • 2
  • 2
Humain

Hôte

  • 5
Lapin

Clonalité

  • 5
Polyclonal

Conjugué

  • 5
Inconjugué

Application

  • 5
  • 5
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB), Dot Blot (DB), Immunoprecipitation (IP), Enzyme Immunoassay (EIA), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunofluorescence (IF)
  • Réactivité croisée (Details)

    Species reactivity (expected):Mouse and Rat.
    Species reactivity (tested):Human.

    Purification

    Protein A Chromatography

    Immunogène

    Fibrils prepared from Human Abeta42 peptide.

    Isotype

    IgG
  • Indications d'application

    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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Conseil sur la manipulation

    Avoid repeated freezing and thawing.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Nakajima, Nishitsuji, Kawashima, Kuwabara, Mikawa, Uchimura, Akaji, Kashiwada, Kobayashi, Saito, Sakashita: "The polyphenol (-)-epigallocatechin-3-gallate prevents apoA-IIowa amyloidosis in vitro and protects human embryonic kidney 293 cells against amyloid cytotoxicity." dans: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, Vol. 23, Issue 1, pp. 17-25, (2016) (PubMed).

    Jackson, Onos, Pepper, Graham, Akeson, Byers, Reinholdt, Frankel, Howell: "DBA/2J genetic background exacerbates spontaneous lethal seizures but lessens amyloid deposition in a mouse model of Alzheimer's disease." dans: PLoS ONE, Vol. 10, Issue 5, pp. e0125897, (2016) (PubMed).

    Tang, Dai, He, Doty, Shultz, Sampson, Dai: "MEK guards proteome stability and inhibits tumor-suppressive amyloidogenesis via HSF1." dans: Cell, Vol. 160, Issue 4, pp. 729-44, (2015) (PubMed).

  • Antigène

    Amyloid Fibrils

    Sujet

    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: Fibrils, OC
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