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APP Antikörper

Der Kaninchen Polyklonal Anti-APP-Antikörper wurde für WB, ELISA, IHC, IF und IP validiert. Er ist geeignet, APP in Proben von Human zu detektieren. Es sind 3+ Publikationen verfügbar.
Rockland
Produktnummer ABIN6655141
Hersteller Produkt- Nr.: 200-401-e87

Kurzübersicht für APP Antikörper (ABIN6655141)

Target

Alle APP Antikörper anzeigen
APP (Amyloid beta (A4) Precursor Protein (APP))

Reaktivität

  • 259
  • 117
  • 112
  • 11
  • 9
  • 8
  • 8
  • 8
  • 8
  • 7
  • 6
  • 5
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 214
  • 86
  • 4
  • 4
  • 3
  • 2
Kaninchen

Klonalität

  • 231
  • 80
  • 1
Polyklonal

Konjugat

  • 175
  • 26
  • 20
  • 18
  • 7
  • 6
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Dieser APP Antikörper ist unkonjugiert

Applikation

  • 200
  • 150
  • 95
  • 52
  • 52
  • 48
  • 44
  • 42
  • 33
  • 28
  • 15
  • 6
  • 5
  • 5
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)
  • Hersteller Produkt- Nr.

    200-401-e87

    Hersteller

    Rockland

    Verwendungszweck

    Amyloid Fibrils (OC) Antibody

    Kreuzreaktivität (Details)

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

    Aufreinigung

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

    Sterilität

    Sterile filtered

    Immunogen

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

    Isotyp

    IgG
  • Applikationshinweise

    Immunoprecipitation_Dilution: User Optimized

    ELISA_Dilution: 1:200

    Immunohistochemistry_Dilution: User Optimized

    Western_Blot_Dilution: 1:1000

    Kommentare

    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.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • 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

    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,-20 °C

    Informationen zur Lagerung

    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.

    Haltbarkeit

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

    Nnah, Lee, Wessling-Resnick: "Iron potentiates microglial interleukin-1β secretion induced by amyloid-β." in: 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." in: Sensors (Basel, Switzerland), Vol. 18, Issue 6, (2018) (PubMed).

  • Target

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

    Andere Bezeichnung

    APP

    Hintergrund

    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 Kaskade in der Apoptose, EGFR Signaling Pathway, Transition Metal Ion Homeostasis, Skeletal Muscle Fiber Development, Toll-Like Receptors Cascades, Feeding Behaviour
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