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InnoZyme™ Myeloperoxidase Activity Assay Kit (Cat. No. CBA024)
 
  
 
  
Ask A Technical ScientistMyeloperoxidase [MPO, (EC1.11.1.7)] is one of a number of enzymes located in the azurophil granules of polymorphonuclear leukocytes (PMNs, also called neutrophils) and, to a lesser extent, in monocytes. MPO catalyzes the formation of hypochlorous acid (HOCl), a powerful oxidant formed from chloride ions and hydrogen peroxide. MPO generates reactive oxygen species as part of its function in innate host defense mechanisms, however, in an unregulated state, it is capable of causing tissue destruction, inflammation, and has been implicated in numerous diseases, including atherosclerosis, cancer, and Alzheimer’s disease.

The InnoZyme™ Myeloperoxidase Activity Kit is a sensitive and specific kit for quantitative measurements of human MPO activity in a variety of cell lysates and fluids. The kit may also be used to screen enzyme inhibitors. The InnoZyme Myeloperoxidase assay uses a specific polyclonal antibody immobilized on a 96-well plate to capture MPO. Activity is detected by colorimetric reaction.

  • Highly selective: based on immunocapture of human MPO
  • Highly sensitive and quantitative: assay range 5–100 ng/ml
  • Versatile: measures human MPO activity in a variety of cell lysates and biological samples
  • Convenient: 96-well format and non-radioactive detection
  • Useful: enables high-throughput screening of human MPO inhibitors
 
 
Line graph showing MPO standard curve

MPO Standard Curve
MPO activity was measured using the InnoZyme Myeloperoxidase Activity Kit. The asterisk (*) identifies a data point common with the MPO (100 ng/ml) standard sample in the figure below.

 
Bar graphs showing MPO activity in biological samples in the absence and presence of MPO inhibitor, ABAH.
MPO Activity in the Absence and Presence of an ABAH Inhibitor
MPO activity was measured (as described in the detailed protocol in the Product Insert) in the absence and presence of 20 µM [4-aminobenzoyl hydrazide, (ABAH)], an irreversible inhibitor of MPO. Cells were cultured in RPMI 1600 medium containing 10% FCS and harvested at 80–90% confluency.The asterisk (*) identifies the 100 ng/ml data point common to that shown in the MPO standard curve above.
 
  
  
 
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