Abstract
A fluorogenic substrate and trapping reagent have been used to detect β-galactosidase activity expressed in S. cerevisiae from an Escherichia coli lacZ gene segment encoded on a recombinant plasmid. The measurement may be made in less than 1 msec using a flow cytometer, facilitating rapid experimental characterization of plasmid instability.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 43-48 |
| Number of pages | 6 |
| Journal | Biotechnology Letters |
| Volume | 5 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 1983 |
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