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IHC-P analysis of human cerebellum using GTX89224 CYP26B1 antibody, Internal. Antigen retrieval : Tris/EDTA buffer pH 9 Dilution : 4microg/ml
IHC-P analysis of human cerebellum using GTX89224 CYP26B1 antibody, Internal. Antigen retrieval : Tris/EDTA buffer pH 9 Dilution : 4microg/ml
IHC-P analysis of human cerebellum using GTX89224 CYP26B1 antibody, Internal. Antigen retrieval : Tris/EDTA buffer pH 9 Dilution : 4microg/ml

CYP26B1 antibody, Internal

GTX89224
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetCYP26B1
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Overview

  • Supplier
    GeneTex
  • Product Name
    CYP26B1 antibody, Internal
  • Delivery Days Customer
    7
  • Application Supplier Note
    IHC-P: 4-6microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID56603
  • Target name
    CYP26B1
  • Target description
    cytochrome P450 family 26 subfamily B member 1
  • Target synonyms
    CYP26A2; cytochrome P450 26B1; cytochrome P450 family 26 subfamily A member 1; cytochrome P450 retinoic acid-inactivating 2; cytochrome P450 retinoid metabolizing protein; cytochrome P450, family 26, subfamily B, polypeptide 1; cytochrome P450, subfamily XXVIB, polypeptide 1; P450RAI2; P450RAI-2; retinoic acid-metabolizing cytochrome; RHFCA
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ9NR63
  • Protein Name
    Cytochrome P450 26B1
  • Scientific Description
    This gene encodes a member of the cytochrome P450 superfamily. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. The encoded protein is localized to the endoplasmic reticulum, and functions as a critical regulator of all-trans retinoic acid levels by the specific inactivation of all-trans retinoic acid to hydroxylated forms. Mutations in this gene are associated with radiohumeral fusions and other skeletal and craniofacial anomalies, and increased levels of the encoded protein are associated with atherosclerotic lesions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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