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Perforin 1 antibody

This Rabbit Polyclonal antibody specifically detects Perforin 1 in WB, IHC and IF. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7254750

Quick Overview for Perforin 1 antibody (ABIN7254750)

Target

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

Reactivity

  • 99
  • 25
  • 8
  • 6
  • 6
  • 5
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 62
  • 55
  • 4
Rabbit

Clonality

  • 65
  • 56
Polyclonal

Conjugate

  • 60
  • 14
  • 13
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Perforin 1 antibody is un-conjugated

Application

  • 48
  • 46
  • 38
  • 19
  • 17
  • 13
  • 10
  • 7
  • 6
  • 6
  • 5
  • 4
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human Perforin (NP_001076585.1).

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000 IHC 1:50-1:200 IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

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

    Alternative Name

    Perforin

    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.

    Molecular Weight

    Observed_MW: 70 kDa

    Calculated_MW: 61 kDa

    Gene ID

    5551

    UniProt

    P14222

    Pathways

    Apoptosis, Caspase Cascade in Apoptosis
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