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A rapid and accurate assay for assessing the cytotoxicity of viral proteins

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UNSPECIFIED. (2005) A rapid and accurate assay for assessing the cytotoxicity of viral proteins. JOURNAL OF VIROLOGICAL METHODS, 127 (2). pp. 119-125. ISSN 0166-0934

Full text not available from this repository.
Official URL: http://dx.doi.org/10.1016/j.jviromet.2005.03.016

Abstract

A fluorescence-based assay is presented for measuring the cytoxicity of viral proteins added exogenously to cells. The assay is based on the use of two fluorescent dyes, calcein-AM and ethidium homodimer (EtD-1) to specifically stain living and dead cells respectively and employs fluorescence activated cells sorting (FACS) to achieve a rapid and accurate measurement of the cytotoxic capacity of a potential viral toxin. The assay has been developed using the group B homologue (ADRV-NSP4) of the NSP4 enterotoxin encoded by Group A rotaviruses but should be applicable to assaying any viral protein exhibiting cytotoxic activity. (c) 2005 Elsevier B.V. All rights reserved.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
T Technology > TP Chemical technology
Q Science > QR Microbiology > QR355 Virology
Journal or Publication Title: JOURNAL OF VIROLOGICAL METHODS
Publisher: ELSEVIER SCIENCE BV
ISSN: 0166-0934
Date: August 2005
Volume: 127
Number: 2
Number of Pages: 7
Page Range: pp. 119-125
Identification Number: 10.1016/j.jviromet.2005.03.016
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/6834

Data sourced from Thomson Reuters' Web of Knowledge

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