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Perforin 1 antibody (AA 148-372)

This anti-Perforin 1 antibody is a Mouse Monoclonal antibody detecting Perforin 1 in ELISA and FACS. Suitable for Human.
Catalog No. ABIN7193868

Quick Overview for Perforin 1 antibody (AA 148-372) (ABIN7193868)

Target

See all Perforin 1 (PRF1) Antibodies
Perforin 1 (PRF1) (Perforin 1 (Pore Forming Protein) (PRF1))

Reactivity

  • 116
  • 29
  • 8
  • 8
  • 6
  • 5
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 75
  • 65
  • 3
Mouse

Clonality

  • 77
  • 66
Monoclonal

Conjugate

  • 70
  • 17
  • 15
  • 5
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Perforin 1 antibody is un-conjugated

Application

  • 58
  • 57
  • 38
  • 23
  • 22
  • 18
  • 10
  • 9
  • 7
  • 6
  • 5
  • 4
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
ELISA, Flow Cytometry (FACS)

Clone

6F8C2
  • Binding Specificity

    • 37
    • 8
    • 8
    • 5
    • 5
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 148-372

    Purpose

    PRF1 Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human PRF1 (AA: 148-372) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % 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

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    Perforin 1 (PRF1) (Perforin 1 (Pore Forming Protein) (PRF1))

    Alternative Name

    PRF1

    Background

    This gene encodes a protein with structural similarities to complement component C9 that is important in immunity. This protein forms membrane pores that allow the release of granzymes and subsequent cytolysis of target cells. Whether pore formation occurs in the plasma membrane of target cells or in an endosomal membrane inside target cells is subject to debate. Mutations in this gene are associated with a variety of human disease including diabetes, multiple sclerosis, lymphomas, autoimmune lymphoproliferative syndrome (ALPS), aplastic anemia, and familial hemophagocytic lymphohistiocytosis type 2 (FHL2), a rare and lethal autosomal recessive disorder of early childhood.

    Molecular Weight

    61.3 kDa

    Gene ID

    5551

    UniProt

    P14222

    Pathways

    Apoptosis, Caspase Cascade in Apoptosis
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