Results 211 to 220 of about 1,484,807 (267)
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Identification of cells in culture
American Journal of Hematology, 1976AbstractMost laboratories using cells cultured in vitro maintain multiple cell lines. Such lines should be monitored for species and intraspecies characteristics to prevent invalidation of research work due to incidents of cell line cross‐contamination.This report describes the results obtained when 246 cell cultures were examined for evidence of cross‐
C S, Stulberg +2 more
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Journal of Electron Microscopy Technique, 1988
AbstractMethods for the establishment and growth of renal cell types in culture are reviewed, with emphasis on current trends. General techniques available for the isolation and culture of glomerular cells have progressed from explant to enzyme dissociation and cloning techniques.
J I, Kreisberg, P D, Wilson
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AbstractMethods for the establishment and growth of renal cell types in culture are reviewed, with emphasis on current trends. General techniques available for the isolation and culture of glomerular cells have progressed from explant to enzyme dissociation and cloning techniques.
J I, Kreisberg, P D, Wilson
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Experimental Cell Research, 1957
Abstract Gas exchange, introduction of nutrients, and removal of waste products can be regulated in a new device for continuous sustained culture of cells in suspension. Strain L, clone 929, fibroblasts; HeLa cells; and strains KB, and Chang, liver cells were successfully propagated in this device.
S, GRAFF, K S, McCARTY
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Abstract Gas exchange, introduction of nutrients, and removal of waste products can be regulated in a new device for continuous sustained culture of cells in suspension. Strain L, clone 929, fibroblasts; HeLa cells; and strains KB, and Chang, liver cells were successfully propagated in this device.
S, GRAFF, K S, McCARTY
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Science, 2007
Culturing Life . How Cells Became Technologies. By Hannah Landecker . Harvard University Press, Cambridge, MA, 2007. 288 pp. $35, £22.95, €32.30. ISBN 9780674023284. Landecker explores how culturing cells has changed our understanding of individuality, immortality, life, and ...
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Culturing Life . How Cells Became Technologies. By Hannah Landecker . Harvard University Press, Cambridge, MA, 2007. 288 pp. $35, £22.95, €32.30. ISBN 9780674023284. Landecker explores how culturing cells has changed our understanding of individuality, immortality, life, and ...
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Current Opinion in Biotechnology, 1998
Most cells can exhibit a biochemical pathway which mediates their own destruction in a highly controlled and genetically defined manner. In animal cells, a morphologically distinct form of this 'programmed cell death' has been identified and extensively characterised. This phenomenon, which has been named apoptosis, accounts for most of the cell deaths
M, al-Rubeai, R P, Singh
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Most cells can exhibit a biochemical pathway which mediates their own destruction in a highly controlled and genetically defined manner. In animal cells, a morphologically distinct form of this 'programmed cell death' has been identified and extensively characterised. This phenomenon, which has been named apoptosis, accounts for most of the cell deaths
M, al-Rubeai, R P, Singh
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Cell cultures and nephrolithiasis
World Journal of Urology, 1997While the physical chemistry of stone formation has been intensively studied during the last decade, it has become clear that the pathophysiology of renal stone disease cannot be explained by crystallization processes only. In recent years, evidence has emerged that the cells lining the renal tubules can have an active role in creating the conditions ...
Verkoelen, CF +3 more
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Molecular and Cellular Biochemistry, 1981
Cellular research in aging has been stimulated by the observation that human diploid cells have a limited number of cell divisions in culture. This loss of cellular proliferation (in vitro senescence) has been extensively studied by biochemical, clonal, and genetic analysis.
M, Reff, E L, Schneider
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Cellular research in aging has been stimulated by the observation that human diploid cells have a limited number of cell divisions in culture. This loss of cellular proliferation (in vitro senescence) has been extensively studied by biochemical, clonal, and genetic analysis.
M, Reff, E L, Schneider
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Current Opinion in Biotechnology, 2014
Microfluidic techniques allow precise control of fluids and particles at the nanoliter scale and facilitate simultaneous manipulation and analysis of cultured cells, starting from a single cell to larger populations and to intact tissues. The use of integrated microfluidic devices has considerably advanced the fields of quantitative and systems biology.
Mehling, Matthias, Tay, Savaş
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Microfluidic techniques allow precise control of fluids and particles at the nanoliter scale and facilitate simultaneous manipulation and analysis of cultured cells, starting from a single cell to larger populations and to intact tissues. The use of integrated microfluidic devices has considerably advanced the fields of quantitative and systems biology.
Mehling, Matthias, Tay, Savaş
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2011
The parathyroid cells are highly differentiated with more or less their only function to secrete parathyroid hormone in response to the extracellular calcium level. Tumours from the parathyroid glands are >99% benign, and have a slow proliferation rate.
Peyman, Björklund, Per, Hellman
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The parathyroid cells are highly differentiated with more or less their only function to secrete parathyroid hormone in response to the extracellular calcium level. Tumours from the parathyroid glands are >99% benign, and have a slow proliferation rate.
Peyman, Björklund, Per, Hellman
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2011
Microbial contamination is a major issue in cell culture, but there are a range of procedures which can be adopted to prevent or eliminate contamination. Contamination may arise from the operator and the laboratory environment, from other cells used in the laboratory, and from reagents.
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Microbial contamination is a major issue in cell culture, but there are a range of procedures which can be adopted to prevent or eliminate contamination. Contamination may arise from the operator and the laboratory environment, from other cells used in the laboratory, and from reagents.
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