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Perforin 1 antibody (AA 9-184)

This anti-Perforin 1 antibody is a Rabbit Polyclonal antibody detecting Perforin 1 in WB. Suitable for Human.
Catalog No. ABIN1886703

Quick Overview for Perforin 1 antibody (AA 9-184) (ABIN1886703)

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

  • 76
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  • 3
Rabbit

Clonality

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  • 65
Polyclonal

Conjugate

  • 70
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  • 5
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  • 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

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  • 1
  • 1
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  • 1
Western Blotting (WB)
  • Binding Specificity

    • 37
    • 8
    • 8
    • 5
    • 5
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
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    • 1
    AA 9-184

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 9 and 184 of Perforin 1
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

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

    Alternative Name

    Perforin 1

    Background

    The protein encoded by this gene has structural and functional similarities to complement component 9 (C9).Like C9, this protein creates transmembrane tubules and is capable of lysing non-specifically a variety of target cells.This protein is one of the main cytolytic proteins of cytolytic granules, and it is known to be a key effector molecule for T-cell- and natural killer-cell-mediated cytolysis.Defects in this gene cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare and lethal autosomal recessive disorder of early childhood.Alternative splicing results in multiple transcript variants encoding the same protein.[provided by RefSeq]
    Synonyms: HPLH2, MGC65093, P1, PFP

    Molecular Weight

    61 kDa

    Gene ID

    5551

    NCBI Accession

    NM_005041, NP_005032

    Pathways

    Apoptosis, Caspase Cascade in Apoptosis
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