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ICC/IF analysis of A431 cells using GTX31576 FKBP12 antibody. Working concentration : 5 microg/ml
ICC/IF analysis of A431 cells using GTX31576 FKBP12 antibody. Working concentration : 5 microg/ml
ICC/IF analysis of A431 cells using GTX31576 FKBP12 antibody. Working concentration : 5 microg/ml

FKBP12 antibody

GTX31576
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry
Product group Antibodies
TargetFKBP1A
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Overview

  • Supplier
    GeneTex
  • Product Name
    FKBP12 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1 - 2 microg/mL. ICC/IF: 5 microg/mL. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID2280
  • Target name
    FKBP1A
  • Target description
    FKBP prolyl isomerase 1A
  • Target synonyms
    12 kDa FK506-binding protein; 12 kDa FKBP; calstabin-1; FK506 binding protein 1A, 12kDa; FK506 binding protein12; FK506-binding protein 1; FK506-binding protein 12; FK506-binding protein 1A; FK506-binding protein, T-cell, 12-kD; FKBP1; FKBP12; FKBP-12; FKBP12-Exip3; FKBP-1A; immunophilin FKBP12; peptidyl-prolyl cis-trans isomerase FKBP1A; PKC12; PKCI2; PPIASE; PPIase FKBP1A; protein kinase C inhibitor 2; rotamase
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP62942
  • Protein Name
    Peptidyl-prolyl cis-trans isomerase FKBP1A
  • Scientific Description
    The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It interacts with several intracellular signal transduction proteins including type I TGF-beta receptor. It also interacts with multiple intracellular calcium release channels, and coordinates multi-protein complex formation of the tetrameric skeletal muscle ryanodine receptor. In mouse, deletion of this homologous gene causes congenital heart disorder known as noncompaction of left ventricular myocardium. Multiple alternatively spliced variants, encoding the same protein, have been identified. The human genome contains five pseudogenes related to this gene, at least one of which is transcribed. [provided by RefSeq, Sep 2008]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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