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APP anticorps

L’anticorps Lapin Polyclonal anti-APP a été validé pour WB, ELISA, IHC, IF et IP. Il convient pour détecter APP dans des échantillons de Humain. Il y a 3+ publications disponibles.
Rockland
N° du produit ABIN6655141
N° du produit (Fournisseur): 200-401-e87

Aperçu rapide pour APP anticorps (ABIN6655141)

Antigène

Voir toutes APP Anticorps
APP (Amyloid beta (A4) Precursor Protein (APP))

Reactivité

  • 239
  • 114
  • 112
  • 11
  • 9
  • 8
  • 8
  • 8
  • 8
  • 7
  • 6
  • 5
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 204
  • 73
  • 4
  • 4
  • 3
  • 2
Lapin

Clonalité

  • 222
  • 66
  • 1
Polyclonal

Conjugué

  • 153
  • 26
  • 19
  • 18
  • 7
  • 6
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Cet anticorp APP est non-conjugé

Application

  • 186
  • 136
  • 82
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  • 43
  • 42
  • 34
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  • 19
  • 15
  • 6
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  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)
  • N° du produit (Fournisseur)

    200-401-e87

    Fournisseur

    Rockland

    Fonction

    Amyloid Fibrils (OC) Antibody

    Réactivité croisée (Details)

    A BLAST analysis was used to suggest cross-reactivity with Amyloid Fibrils (OC) from Human based on 100 % homology with the immunizing sequence.

    Purification

    Anti-Amyloid Fibrils (OC) Antibody was purified by Protein A chromatography.

    Stérilité

    Sterile filtered

    Immunogène

    Amyloid Fibrils (OC) Antibody was produced from whole rabbit serum prepared by repeated immunizations with fibrils prepared from human Abeta42 synthetic peptide.

    Isotype

    IgG
  • Indications d'application

    Immunoprecipitation_Dilution: User Optimized

    ELISA_Dilution: 1:200

    Immunohistochemistry_Dilution: User Optimized

    Western_Blot_Dilution: 1:1000

    Commentaires

    Suggested Applications: Other
    Anti-Amyloid Fibrils (OC) Antibody is tested for use in IP, IF microscopy, IHC, and WB. Specific conditions for reactivity should be optimized by the end user.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2

    Stabilizer: 50 % (v/v) Glycerol

    Preservative: 0.09 % (w/v) Sodium Azide

    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.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store vial at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.

    Date de péremption

    12 months
  • Lee, Park, Kim, Lee, Lee, Hwang, Lee, Lee, Yoon: "Plasmonic nanoparticle amyloid corona for screening Aβ oligomeric aggregate-degrading drugs." dans: Nature communications, Vol. 12, Issue 1, pp. 639, (2021) (PubMed).

    Nnah, Lee, Wessling-Resnick: "Iron potentiates microglial interleukin-1β secretion induced by amyloid-β." dans: Journal of neurochemistry, Vol. 154, Issue 2, pp. 177-189, (2020) (PubMed).

    Jeong, Kim, Chae, Lee, Yang, Kim, Kim, Lee, Lee, Choi, Yoon, Hwang: "Multifunctionalized Reduced Graphene Oxide Biosensors for Simultaneous Monitoring of Structural Changes in Amyloid-β 40." dans: Sensors (Basel, Switzerland), Vol. 18, Issue 6, (2018) (PubMed).

  • Antigène

    APP (Amyloid beta (A4) Precursor Protein (APP))

    Autre désignation

    APP

    Sujet

    Synonyms: Amyloid OC, Fibrils, Amyloid Oligomer αβ, A11, Amyloid beta A4 protein, ABPP, APPI, Alzheimer disease amyloid protein, Cerebral vascular amyloid peptide, PreA4, Protease nexin-II, APP, A4, AD1

    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. 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.

    Gene Name: APP

    UniProt

    P05067

    Pathways

    Caspase Cascade in Apoptosis, EGFR Signaling Pathway, Transition Metal Ion Homeostasis, Skeletal Muscle Fiber Development, Toll-Like Receptors Cascades, Feeding Behaviour
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