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PRNP antibody

The Rabbit Polyclonal anti-PRNP antibody (ABIN7249118) specifically detects PRNP in IHC and ELISA. The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7249118
-15% Promotion 2026
$457.98
$538.80
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Quick Overview for PRNP antibody (ABIN7249118)

Target

See all PRNP Antibodies
PRNP (Prion Protein (PRNP))

Reactivity

  • 123
  • 70
  • 54
  • 20
  • 13
  • 9
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 106
  • 31
  • 16
  • 2
  • 2
  • 1
Rabbit

Clonality

  • 80
  • 78
Polyclonal

Conjugate

  • 61
  • 11
  • 9
  • 6
  • 6
  • 5
  • 5
  • 5
  • 5
  • 5
  • 5
  • 5
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This PRNP antibody is un-conjugated

Application

  • 77
  • 38
  • 35
  • 27
  • 26
  • 19
  • 15
  • 15
  • 15
  • 9
  • 7
  • 3
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Fusion protein of human PRNP

    Isotype

    IgG
  • Application Notes

    IHC 1:30-1:150, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.6 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    PRNP (Prion Protein (PRNP))

    Alternative Name

    PRNP

    Background

    The protein encoded by this gene is a membrane glycosylphosphatidylinositol-anchored glycoprotein that tends to aggregate into rod-like structures. The encoded protein contains a highly unstable region of five tandem octapeptide repeats. This gene is found on chromosome 20, approximately 20 kbp upstream of a gene which encodes a biochemically and structurally similar protein to the one encoded by this gene. Mutations in the repeat region as well as elsewhere in this gene have been associated with Creutzfeldt-Jakob disease, fatal familial insomnia, Gerstmann-Straussler disease, Huntington disease-like 1, and kuru. An overlapping open reading frame has been found for this gene that encodes a smaller, structurally unrelated protein, AltPrp. Alternative splicing results in multiple transcript variants.

    UniProt

    P04156

    Pathways

    Transition Metal Ion Homeostasis, Activated T Cell Proliferation
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