We describe two alternative assays for measuring collagenolytic activity using 3 H-acetylated collagen. Both assays have been developed for the 96-well plate format and measure the amount of radiolabeled collagen fragments released into the supernatant from an insoluble 3 H-acetylated collagen fibri
A semiautomated, 96-well plate assay for collagen synthesis
โ Scribed by Andrew Scutt; Annemarie Berg; Hubert Mayer
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 532 KB
- Volume
- 203
- Category
- Article
- ISSN
- 0003-2697
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โฆ Synopsis
We have established a rapid method for the measurement of collagen synthesis in large numbers of cell cultures. 3H-labeled collagen in microwell cultures was salt precipitated, harvested, and washed using a commercially available cell harvester and the filtered collagen was directly counted. The cell number could then be assessed either by methylene blue staining or by dissolving the cells in NaOH and estimating the protein content with bicinchoninic acid. In all of these procedures, the samples remain in microtiter plates, thus ensuring that minimal amounts of reagents are used and minimizing the amount of manipulation necessary. The intergroup variability is 3 to 9% and the recovery of 3H-labeled collagen is greater than 90%. Using this method, large numbers of samples can be assessed for collagen synthesis quickly, conveniently, and for minimal cost.
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