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IHC-P analysis of human liver carcinoma tissue using GTX04688 PMP22 antibody [OTI5D1]. Antigen retrieval : Heat mediated 1mM EDTA in 10mM Tris buffer (pH 8.5) Dilution : 1:2000
IHC-P analysis of human liver carcinoma tissue using GTX04688 PMP22 antibody [OTI5D1]. Antigen retrieval : Heat mediated 1mM EDTA in 10mM Tris buffer (pH 8.5) Dilution : 1:2000
IHC-P analysis of human liver carcinoma tissue using GTX04688 PMP22 antibody [OTI5D1]. Antigen retrieval : Heat mediated 1mM EDTA in 10mM Tris buffer (pH 8.5) Dilution : 1:2000

PMP22 antibody [OTI5D1]

GTX04688
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetPMP22
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Overview

  • Supplier
    GeneTex
  • Product Name
    PMP22 antibody [OTI5D1]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500. IHC-P: 1:2000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    OTI5D1
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID5376
  • Target name
    PMP22
  • Target description
    peripheral myelin protein 22
  • Target synonyms
    Charcot-Marie-Tooth neuropathy 1A (greatly reduced nerve conduction velocity, hereditary motor sensory neuropathy Ia); CIDP; CMT1A; CMT1E; DSS; GAS3; GAS-3; growth arrest-specific protein 3; HMSNIA; HNPP; peripheral myelin protein 22; peripheral myelin protein 22 kDa; Sp110
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDQ01453
  • Protein Name
    Peripheral myelin protein 22
  • Scientific Description
    This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203