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Recruitment of the GFP fusion proteins to MIR-induced DNA damage tracks was monitored in live cells.
Thus, molecular interactions and processes that were approached by biochemical analyses in vitro can now be directly monitored in live cells.
Ad5-yCD/mutTK(SR39)rep-hNIS Ad5-yCD/mutTK SR39 rep-hNIS Ad5-yCD/mutTK SR39 rep-hNIShNIS) were injected into contrAd5-yCD/mutTK SR39 rep-hNISrostand and hNIS activity was monitored in live animals following administration of Na(99m)TcO(4) using gamma camera scintigraphNIS
To test this assumption, the localization of proteasomes (by using Mts4 as an indicator) and Vpr was monitored in live cells of the cut8 mutant expressing the GFP-Vpr and GFP-Mts4 fusions.
Collagen I degradation was monitored in live cells migrating through a native 3D collagen substrate.
In parallel experiments, Ca2+ sparks were monitored in live permeabilized myocytes.
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Stauffer, T. P., Ahn, S. & Meyer, T. Receptor-induced transient reduction in plasma membrane PtdIns(4,5 P2 concentration monitored in living cells.
Through the specific labeling of proteins on the PM, the process of endocytosis can be tracked and monitored in living cells.
These two PIP2 reporters were specifically expressed in SOPs using the UAS/GAL4 system [23] and their localization was monitored in living pupae.
Cellular uptake substances were monitored in living cells placed in a chamber at 37 °C within 1 h.
In our study, the intracellular localization of TAT-SA was monitored in living HeLa cells with various fluorescent endocytic markers.
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