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IHC-P analysis of human follicular lymphoma using GTX01949 Perforin antibody [5B10]. Note focal granular staining of occasional cytotoxic T lymphocytes.
IHC-P analysis of human follicular lymphoma using GTX01949 Perforin antibody [5B10]. Note focal granular staining of occasional cytotoxic T lymphocytes.
IHC-P analysis of human follicular lymphoma using GTX01949 Perforin antibody [5B10]. Note focal granular staining of occasional cytotoxic T lymphocytes.

Perforin antibody [5B10]

GTX01949
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetPRF1
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Overview

  • Supplier
    GeneTex
  • Product Name
    Perforin antibody [5B10]
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibofy shows cross-reactivity with smooth muscle and differentiated epithelium.
  • Application Supplier Note
    IHC-P: 1:20. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    5B10
  • Conjugate
    Unconjugated
  • Gene ID5551
  • Target name
    PRF1
  • Target description
    perforin 1
  • Target synonyms
    cytolysin; HPLH2; lymphocyte pore-forming protein; P1; perforin 1 (pore forming protein); perforin-1; PFP
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDP14222
  • Protein Name
    Perforin-1
  • Scientific Description
    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. [provided by RefSeq, Aug 2017]
  • Reactivity
    Human
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352203