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The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using CSB-PA829442(GLO1 Antibody) at dilution 1/60, on the right is treated with fusion protein. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using CSB-PA829442(GLO1 Antibody) at dilution 1/60, on the right is treated with fusion protein. (Original magnification: x200)
The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using CSB-PA829442(GLO1 Antibody) at dilution 1/60, on the right is treated with fusion protein. (Original magnification: x200)

GLO1 Antibody

CSB-PA829442
Cusabio
ApplicationsWestern Blot, ELISA, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetGLO1
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Overview

  • Supplier
    Cusabio
  • Product Name
    GLO1 Antibody
  • Delivery Days Customer
    20
  • Applications
    Western Blot, ELISA, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID2739
  • Target name
    GLO1
  • Target description
    glyoxalase I
  • Target synonyms
    aldoketomutase; epididymis secretory protein Li 74; GLOD1; glx I; GLYI; glyoxalase domain containing 1; HEL-S-74; ketone-aldehyde mutase; lactoyl glutathione lyase; lactoylglutathione lyase; methylglyoxalase; S-D-lactoylglutathione methylglyoxal lyase
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ04760
  • Protein Name
    Lactoylglutathione lyase
  • Scientific Description
    The enzyme encoded by this gene is responsible for the catalysis and formation of S-lactoyl-glutathione from methylglyoxal condensation and reduced glutatione. Glyoxalase I is linked to HLA and is localized to 6p21.3-p21.1, between HLA and the centromere.
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    41116161

FAQ

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Figure 1. Western blot analysis of GLO1 using anti-GLO1 antibody (A01703-1). 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 Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human COLO320 whole cell lysates, Lane 4: human 22RV1 whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: human A431 whole cell lysates, Lane 7: human U937 whole cell lysates, Lane 8: human THP-1 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-GLO1 antigen affinity purified polyclonal antibody (Catalog # A01703-1) 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 GLO1 at approximately 21 kDa. The expected band size for GLO1 is at 21 kDa.
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