PSA is an important tumor-marker for prostatic cancer disease. We developed a sensitive, simple and inexpensive Sandwich ELISA for PSA with two monoclonal antibodies. The precision and reliability of the assay are reflected in the low inter- and intraassay coefficient of variation. PSA was not detec
Use of enzyme immunoassay for measurement of skeletal troponin-I utilizing isoform-specific monoclonal antibodies
โ Scribed by Miyoko Takahashi; Lilian Lee; Qinwei Shi; Yehia Gawad; George Jackowski
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 830 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0009-9120
No coin nor oath required. For personal study only.
โฆ Synopsis
Objective:
To determine the serum level of fast skeletal troponin i (fstnl) resulting from skeletal muscle damage, we have developed a sensitive two-site enzyme immunoassay to measure skeletal troponin i.
Design and methods:
Twelve monoclonal antibodies were raised against human fstnl. of these antibodies, 8 were fstnl-specific and the remaining 4 reacted with both skeletal and cardiac troponin i (ctnl). two monoclonals were utilized for a development of this fstnl immunoassay. standards were made with purified recombinant human fstnl for the range of 0-25 micrograms/ml.
Results:
Total assay variance (cv) ranged from 1.7% to 9.6%. the upper limit of the normal reference range was established as 0.2 microgram/l by determining fstnl concentration in sera of 108 healthy donors without evidence of muscle damage. purified human ctnl up to 500 micrograms/l and ctnl-positive clinical serum samples yielded negative results in the fstnl assay. the serum levels of fstnl were determined in trauma patients, patients with chronic degenerative muscle disease, and marathon runners. in the study populations, the serum levels of fstnl were correlated with other biochemical markers that are traditionally used to monitor striated muscle damage.
Conclusions:
In the present preliminary studies, measuring the serum levels of fstnl in patients with various forms of muscle damage is more accurate than using the classical non muscle-specific biochemical markers.
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