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Development of Multiple-Well Plate Biological Assays

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Protocols for Neural Cell Culture

Part of the book series: Springer Protocols Handbooks ((SPH))

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Abstract

This chapter focuses on the application of multiple-well plate technology to biological assays for neuroactive or other agents. It does not attempt to address specific cell types, culture systems, or individual assays for neurotoxicity, neural cell differentiation, or other applications of neuronal cells in culture. These topics are far too broad. Other chapters in this book provide that information. Rather, this chapter provides points to consider in developing the bioassay of interest in the multiple-well plate format. It highlights many of the issues that must be addressed both to reduce the size of the individual cultures and to use end point assays, which can readily be instrument-scored. The term “end point assay” refers to the specific method used to measure the induced change in the cells. Multiple-well plates of 96 or more wells per plate are not new, nor are the bioassays based on them. However, the physical dimensions of the wells, the need for uniformity among wells, and the frequent focus on spectrophotometric or fluorometric end points require special attention in the experimental design.

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Further Reading

  • Alagarsamy, S., Phillips, M., Pappas, T., and Johnson, K. M. (1997), Dopamine neutrotoxicity in cortical neurons. Drug Alcohol Dependence 48, 105–111.

    Article  CAS  Google Scholar 

  • Berridge, M. V., Tan, A. S., McCoy, K. D., and Wang, R. (1996), The biochemical and cellular basis of cell proliferation assays that use tetrazolium salts. Boehringer Mannheim Biochemica 4, 14–23.

    Google Scholar 

  • Marshall, N. J., Goodwin, C. J., and Holt, S. J. (1995), A critical assessment of the use of microculture tetrazolium assays to measure cell growth and function. Growth Regulation 5, 69–84.

    PubMed  CAS  Google Scholar 

  • McConnel, H. M., Owicki, J. C., Parce, J. W., Miller, D. L., Baxter, G. T., Wada, H. G., and Pitchford, S. (1992), The Cytosensor microphysiometer: biological applications of silicon technology. Science 257, 1906–1912.

    Article  Google Scholar 

  • Mosmann, T. (1983), Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 65, 55–63.

    Article  PubMed  CAS  Google Scholar 

  • Shopsis, C. and Eng, B. (1985), Rapid cytotoxicity testing using a semi-automated protein determination on cultured cells. Toxicol. Lett. 26, 1–8.

    Article  PubMed  CAS  Google Scholar 

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© 2001 Humana Press Inc., Totowa, NJ

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Harbell, J.W. (2001). Development of Multiple-Well Plate Biological Assays. In: Fedoroff, S., Richardson, A. (eds) Protocols for Neural Cell Culture. Springer Protocols Handbooks. Humana Press. https://doi.org/10.1385/1-59259-207-4:265

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  • DOI: https://doi.org/10.1385/1-59259-207-4:265

  • Publisher Name: Humana Press

  • Print ISBN: 978-0-89603-902-5

  • Online ISBN: 978-1-59259-207-4

  • eBook Packages: Springer Book Archive

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