Abstract
A protocol was developed to achieve the simultaneous determination of gene expression and bacterial identity at the level of single cells: a chromogenic beta-galactosidase activity assay was combined with in situ hybridization of Fluorescently labelled oligonucleotide probes to rRNA. The method allows monitoring of gene expression and quantification of beta-galactosidase activity in single cells.
Original language | English |
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Journal | Applied and Environmental Microbiology |
Volume | 63 |
Issue number | 9 |
Pages (from-to) | 3698-3702 |
ISSN | 0099-2240 |
Publication status | Published - 1997 |