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      Biological potential of hydroalcoholic extracts of Physalis pubescens L

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          Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

          A tetrazolium salt has been used to develop a quantitative colorimetric assay for mammalian cell survival and proliferation. The assay detects living, but not dead cells and the signal generated is dependent on the degree of activation of the cells. This method can therefore be used to measure cytotoxicity, proliferation or activation. The results can be read on a multiwell scanning spectrophotometer (ELISA reader) and show a high degree of precision. No washing steps are used in the assay. The main advantages of the colorimetric assay are its rapidity and precision, and the lack of any radioisotope. We have used the assay to measure proliferative lymphokines, mitogen stimulations and complement-mediated lysis.
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            Use of a free radical method to evaluate antioxidant activity

            LWT - Food Science and Technology, 28(1), 25-30
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              Pathogenic Escherichia coli.

              Few microorganisms are as versatile as Escherichia coli. An important member of the normal intestinal microflora of humans and other mammals, E. coli has also been widely exploited as a cloning host in recombinant DNA technology. But E. coli is more than just a laboratory workhorse or harmless intestinal inhabitant; it can also be a highly versatile, and frequently deadly, pathogen. Several different E. coli strains cause diverse intestinal and extraintestinal diseases by means of virulence factors that affect a wide range of cellular processes.
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                Author and article information

                Journal
                Biocatalysis and Agricultural Biotechnology
                Biocatalysis and Agricultural Biotechnology
                Elsevier BV
                18788181
                January 2021
                January 2021
                : 31
                : 101895
                Article
                10.1016/j.bcab.2020.101895
                5acfd3bf-9473-4e93-bda2-09966d55f21a
                © 2021

                https://www.elsevier.com/tdm/userlicense/1.0/

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