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Anti-MUS81 Antibody

144-06818
RayBiotech
ApplicationsWestern Blot, ImmunoHistoChemistry
Product group Antibodies
TargetMUS81
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Overview

  • Supplier
    RayBiotech
  • Product Name
    Anti-MUS81 Antibody
  • Delivery Days Customer
    16
  • Applications
    Western Blot, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID80198
  • Target name
    MUS81
  • Target description
    MUS81 structure-specific endonuclease subunit
  • Target synonyms
    crossover junction endonuclease MUS81; MUS81 endonuclease homolog; SLX3; SLX3 structure-specific endonuclease subunit homolog
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ96NY9
  • Protein Name
    Crossover junction endonuclease MUS81
  • Scientific Description
    MUS81 Polyclonal Antibody
  • Storage Instruction
    -20°C
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of MUS81 using anti-MUS81 antibody (A00810-1). 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: rat brain tissue 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-MUS81 antigen affinity purified polyclonal antibody (Catalog # A00810-1) 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 MUS81 at approximately 70 kDa. The expected band size for MUS81 is at 61 kDa.
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IHC image of CSB-PA836272LA01HU diluted at 1:300 and staining in paraffin-embedded human brain tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
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