Abstract
An overview is given on the possibility to measure fluorescence dynamics of cellular proteins with high spatial/temporal resolution. It is shown that such measurement capability yield useful guidelines in designing proper controls for quantitative live cell imaging such as FRET microscopy and in situ pH imaging.
Original language | English (US) |
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Pages (from-to) | 4658-4660 |
Number of pages | 3 |
Journal | Applied Physics Letters |
Volume | 83 |
Issue number | 22 |
DOIs | |
State | Published - Dec 1 2003 |