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APP antibody (N-Term)

This anti-APP antibody is a Rabbit Polyclonal antibody detecting APP in WB, IHC (p) and FACS. Suitable for Mouse.
Catalog No. ABIN2840726

Quick Overview for APP antibody (N-Term) (ABIN2840726)

Target

See all APP Antibodies
APP (Amyloid beta (A4) Precursor Protein (APP))

Reactivity

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Mouse

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This APP antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Clone

RB5012
  • Binding Specificity

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    AA 29-61, N-Term

    Predicted Reactivity

    Pr

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This APP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 29-61 amino acids from the N-terminal region of human APP.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:2000. IHC-P: 1:10~50. FC: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

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

    Alternative Name

    APP

    Background

    APP is a cell surface receptor and transmembrane precursor protein that is cleaved by secretases to form a number of peptides. Some of these peptides are secreted and can bind to the acetyltransferase complex APBB1/TIP60 to promote transcriptional activation, while others form the protein basis of the amyloid plaques found in the brains of patients with Alzheimer disease. Mutations in this gene have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy).

    Molecular Weight

    86943

    Gene ID

    351

    NCBI Accession

    NP_000475, NP_001129488, NP_001129601, NP_001129602, NP_001129603, NP_001191230, NP_001191231, NP_001191232, NP_958816, NP_958817

    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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