Description: MPO, Mouse, ELISA kit
Myeloperoxidase (MPO) is a glycoprotein with a alpha2beta2 heteromultimer expressed in all cells of the myeloid linage. MPO is abundantly present in azurophilic granules of polymorphonuclear neutrophils. It is an important enzyme used during phagocytic lysis of engulfed foreign particles which takes part in the defense of the organism through production of hypochlorous acid (HOCl), a potent oxidant. MPO is rapidly released by activated polymorphonuclear neutrophils. Involvement of MPO has been described in numerous diseases such as atherosclerosis, lung cancer, Alzheimers disease and multiple sclerosis. Autoimmune antibodies to MPO are involved in Wegeners disease. Since the discovery of MPO deficiency, initially regarded as rare and restricted to patients suffering from severe infections, MPO has attracted more clinical attention.Specifications:
| HK210-02 |
| Assays |
| 2 x 96 det. |
| 1.6-100 ng/ml |
| 1.6 ng/ml |
| 100 µl/well |
| Mouse |
| Rat - Weak |
| The mouse MPO ELISA kit is to be used for the in vitro quantitative determination of mouse MPO in plasma, tissue homogenate and cell culture supernatant samples. Note that most reliable results are obtained with heparin plasma. |
| Cardiology and metabolism, Pulmonology |
| The mouse MPO ELISA is a ready-to-use solid-phase enzyme-linked immunosorbent assay based on the sandwich principle with a working time of 3½ hours. The efficient format of a plate with twelve disposable 8-well strips allows free choice of batch size for the assay. Samples and standards are incubated in microtiter wells coated with antibodies recognizing mouse MPO. Biotinylated tracer antibody will bind to captured mouse MPO. Streptavidin-peroxidase conjugate will bind to the biotinylated tracer antibody. Streptavidin-peroxidase conjugate will react with the substrate, tetramethylbenzidine (TMB). The enzyme reaction is stopped by the addition of oxalic acid. The absorbance at 450 nm is measured with a spectrophotometer. A standard curve is obtained by plotting the absorbance (linear) versus the corresponding concentrations of the mouse MPO standards (log). The mouse MPO concentration of samples, which are run concurrently with the standards, can be determined from the standard curve. |
| The linearity of the assay was determined by serially diluting a serum sample containing 49.62 ng/ml mouse MPO. The diluted samples were measured in the assay. The line obtained a slope of 1.03 and a correlation coefficient of 0.998. |
| Product should be stored at 4 °C. Under recommended storage conditions, product is stable for one year. |
| For research use only. Not for use in or on humans or animals or for diagnostics. It is the responsibility of the user to comply with all local/state and Federal rules in the use of this product. Hycult Biotech is not responsible for any patent infringements that might result with the use of or derivation of this product. |
| 1. Vries de, B et al; Exogenous alpha-1-acid glycoprotein protects against renal ischemia-reperfusion injury by inhibition of inflammation and apoptosis. Transplantation 2004, 78: 1116 2. Xu, H et al; A coagulation factor Vll deficiency protects against acute inflammatory responses in mice. J Pathol 2006, 210: 488 3. Porras, M et al; Correlation between cyclical epithelial barrier dysfunction and bacterial translocation in the relapses of intestinal inflammation. Inflamm Bowel Dis 2006, 12: 843 4. Brochner, A et al; Effect of renal and non-renal ischemia⁄reperfusion on cell-mediated immunity in organs and plasma. APMIS 2010, 118: 110 5. Dahlke, K et al; Distinct Different Contributions of the Alternative and Classical Complement Activation Pathway for the Innate Host Response during Sepsis. J Immunol 2011 6. Ishizaki, S et al; Role of CD69 in acute lung injury. Life Sciences 2012, 90: 657 |
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