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Please use this identifier to cite or link to this item: http://10.7.186.7:8080/jspui/handle/123456789/36
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dc.contributor.authorHelgason, Cheryl D. (Editor)-
dc.contributor.authorMiller, Cindy L. (editor)-
dc.date.accessioned2015-04-20T11:14:47Z-
dc.date.available2015-04-20T11:14:47Z-
dc.date.issued2015-
dc.identifier.urihttp://edepository.rls.gov.rw/-
dc.identifier.urihttp://edepository.rls.gov.rw/jspui/handle/123456789/36-
dc.descriptionCell culture is an invaluable tool for investigators in numerous fields. It facilitates analysis of biological properties and processes that are not readily accessible at the level of the intact organism. Successful maintenance of cells in culture, whether primary or immortalized, requires knowledge and practice of a few essential techniques. The purpose of this chapter is to explain the basic principles of cell culture using the maintenance of a nonadherent cell line, the P815 mouse mastocytoma cell line, and the isolation and culture of adherent primary mouse embryonic fibroblasts (MEFs) as examples. Procedures for thawing, culture, determination of cell numbers and viability, and cryopreservation are described.en_US
dc.description.abstractThere are four basic requirements for successful cell culture. Each of these will be briefly reviewed in this introduction. However, a more detailed description is beyond the scope of this chapter. Instead, the reader is referred to one of a number of valuable resources that provide the information necessary to establish a tissue culture laboratory, as well as describe the basic principles of sterile technique (1–4). The first necessity is a well-established and properly equipped cell culture facility. The level of biocontainment required (Levels 1–4) is dependent on the type of cells cultured and the risk that these cells might contain, and transmit, infectious agents. For example, culture of primate cells, transformed human cell lines, mycoplasma-contaminated cell lines, and nontested human cells require a minimum of a Level 2 containment facility. All facilities shoulden_US
dc.language.isoenen_US
dc.publisherHumana Pressen_US
dc.subjectCell cultureen_US
dc.subjectnonadherent cell line;en_US
dc.subjectadherent cellsen_US
dc.subjectprimary mouse embryonic fibroblastsen_US
dc.subjecthemocytometeren_US
dc.subjectviabilityen_US
dc.titleBasic Cell Culture Protocolsen_US
dc.typeBooken_US
Appears in Collections:500 - Pure Sciences

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