Towards high-throughput flim for protein-protein interaction screening of live cells and tissue microarrays
Studying cellular protein-protein interactions in situ requires a technique such as fluorescence resonance energy transfer (FRET) which is sensitive on the nanometer scale. Observing FRET is significantly simplified if the fluorescence lifetime of the donor can be monitored. Results from live cells...
Asıl Yazarlar: | Barber, P, Pierce, G, Ameer-Beg, S, Matthews, DR, Carlin, L, Keppler, M, Kelleher, M, Festy, F, Gillett, C, Springall, R, Ng, T, Vojnovic, B, IEEE |
---|---|
Materyal Türü: | Conference item |
Baskı/Yayın Bilgisi: |
2008
|
Benzer Materyaller
-
Dynamic imaging of protein-protein interactions by MP-FLIM
Yazar:: Ameer-Beg, S, ve diğerleri
Baskı/Yayın Bilgisi: (2005) -
A high-content screening platform utilizing polarization anisotropy and FLIM microscopy
Yazar:: Matthews, DR, ve diğerleri
Baskı/Yayın Bilgisi: (2008) -
Multiphoton time-domain fluorescence lifetime imaging microscopy: practical application to protein-protein interactions using global analysis
Yazar:: Barber, P, ve diğerleri
Baskı/Yayın Bilgisi: (2009) -
Multiphoton-FLIM quantification of the EGFP-mRFP1 FRET pair for localization of membrane receptor-kinase interactions.
Yazar:: Peter, M, ve diğerleri
Baskı/Yayın Bilgisi: (2005) -
Deep-tissue multi-photon fluorescence lifetime microscopy for intravital imaging of protein-protein interactions
Yazar:: Fruhwirth, G, ve diğerleri
Baskı/Yayın Bilgisi: (2009)