Bio-Connect
WB analysis of various samples using GTX00779 Mineralocorticoid Receptor antibody. Lane 1 : Rat Kidney Tissue Lysate Lane 2 : Mouse Kidney Tissue Lysate Lane 3 : HeLa Whole Cell Lysate Lane 4 : A431 Whole Cell Lysate Dilution : 0.5 microg/mL Loading : 50microg
WB analysis of various samples using GTX00779 Mineralocorticoid Receptor antibody. Lane 1 : Rat Kidney Tissue Lysate Lane 2 : Mouse Kidney Tissue Lysate Lane 3 : HeLa Whole Cell Lysate Lane 4 : A431 Whole Cell Lysate Dilution : 0.5 microg/mL Loading : 50microg
WB analysis of various samples using GTX00779 Mineralocorticoid Receptor antibody. Lane 1 : Rat Kidney Tissue Lysate Lane 2 : Mouse Kidney Tissue Lysate Lane 3 : HeLa Whole Cell Lysate Lane 4 : A431 Whole Cell Lysate Dilution : 0.5 microg/mL Loading : 50microg

Mineralocorticoid Receptor antibody

GTX00779
GeneTex
ApplicationsWestern Blot
Product group Antibodies
TargetNR3C2
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Overview

  • Supplier
    GeneTex
  • Product Name
    Mineralocorticoid Receptor antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 0.1-0.5microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID4306
  • Target name
    NR3C2
  • Target description
    nuclear receptor subfamily 3 group C member 2
  • Target synonyms
    MCR, MLR, MR, NR3C2VIT, mineralocorticoid receptor, aldosterone receptor, mineralocorticoid receptor 1, mineralocorticoid receptor 2, mineralocorticoid receptor delta
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP08235
  • Protein Name
    Mineralocorticoid receptor
  • Scientific Description
    This gene encodes the mineralocorticoid receptor, which mediates aldosterone actions on salt and water balance within restricted target cells. The protein functions as a ligand-dependent transcription factor that binds to mineralocorticoid response elements in order to transactivate target genes. Mutations in this gene cause autosomal dominant pseudohypoaldosteronism type I, a disorder characterized by urinary salt wasting. Defects in this gene are also associated with early onset hypertension with severe exacerbation in pregnancy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203