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The image on the left is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using CSB-PA183005(SEPN1 Antibody) at dilution 1/20, on the right is treated with synthetic peptide. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using CSB-PA183005(SEPN1 Antibody) at dilution 1/20, on the right is treated with synthetic peptide. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using CSB-PA183005(SEPN1 Antibody) at dilution 1/20, on the right is treated with synthetic peptide. (Original magnification: x200)

SEPN1 Antibody

CSB-PA183005
Cusabio
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry
Product group Antibodies
TargetSELENON
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Overview

  • Supplier
    Cusabio
  • Product Name
    SEPN1 Antibody
  • Delivery Days Customer
    20
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID57190
  • Target name
    SELENON
  • Target description
    selenoprotein N
  • Target synonyms
    CFTD; MDRS1; RSMD1; RSS; selenoprotein N; selenoprotein N, 1; SELN; SEPN1
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9NZV5
  • Protein Name
    Selenoprotein N
  • Scientific Description
    This gene encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3 UTR of selenoprotein genes have a common stem-loop structure, the sec insertion sequence (SECIS), that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal.
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of SELENON using anti-SELENON antibody (A31971-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SELENON antigen affinity purified polyclonal antibody (Catalog # A31971-1) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SELENON at approximately 66-70 kDa. The expected band size for SELENON is at 66-70 kDa.
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