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Probing the endocytic pathway in live cells using dual-color fluorescence cross-correlation analysis
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Here the authors utilize single-photon dual-color cross-correlation spectroscopy on the commercially available ConfoCor2 set up to study the divergence of endocytic pathways using fluorescently labeled cholera toxins.
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Bacia K., Majoul I.V., Schwille P. Probing the endocytic pathway in live cells using dual-color fluorescence cross-correlation analysis. Biophys. J. 83:2002;1184-1193 Here the authors utilize single-photon dual-color cross-correlation spectroscopy on the commercially available ConfoCor2 set up to study the divergence of endocytic pathways using fluorescently labeled cholera toxins.
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(2002)
Biophys. J.
, vol.83
, pp. 1184-1193
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Bacia, K.1
Majoul, I.V.2
Schwille, P.3
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54
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0037022641
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Ligand binding to somatostatin receptors induces receptor-specific oligomer formation in live cells
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Patel R.C., Kumar U., Lamb D.C., Eid J.S., Rocheville M., Grant M., Rani A., Hazlett T., Patel S.C., Gratton E., et al. Ligand binding to somatostatin receptors induces receptor-specific oligomer formation in live cells. Proc. Natl. Acad. Sci. U.S.A. 99:2002;3294-3299.
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(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 3294-3299
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Patel, R.C.1
Kumar, U.2
Lamb, D.C.3
Eid, J.S.4
Rocheville, M.5
Grant, M.6
Rani, A.7
Hazlett, T.8
Patel, S.C.9
Gratton, E.10
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55
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85030952018
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Intracellular measurements of calmodulin and CaMKII interactions using multiphoton fluorescence cross-correlation spectroscopy (MPFCCS)
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Kim S.A., Heinze K.G., Waxham M.N., Schwille P. Intracellular measurements of calmodulin and CaMKII interactions using multiphoton fluorescence cross-correlation spectroscopy (MPFCCS). Biophys. J. 82:2002;44a.
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(2002)
Biophys. J.
, vol.82
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Kim, S.A.1
Heinze, K.G.2
Waxham, M.N.3
Schwille, P.4
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56
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0034641711
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Simultaneous two-photon excitation of distinct labels for dual-color fluorescence crosscorrelation analysis
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Heinze K.G., Koltermann A., Schwille P. Simultaneous two-photon excitation of distinct labels for dual-color fluorescence crosscorrelation analysis. Proc. Natl. Acad. Sci. U.S.A. 97:2000;10377-10382.
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(2000)
Proc. Natl. Acad. Sci. U.S.A.
, vol.97
, pp. 10377-10382
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Heinze, K.G.1
Koltermann, A.2
Schwille, P.3
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57
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0037125999
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A protease assay for two-photon crosscorrelation and FRET analysis based solely on fluorescent proteins
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Two-photon excitation is combined with FRET and cross-correlation analysis for measuring a new protease assay formed on the basis of genetically encodable intrinsically fluorescent proteins. A fusion protein consisting of eGFP and DsRed separated by a peptide with a protease cleavage site was monitored for proteolytic degradation in real-time using this combination of techniques.
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Kohl T., Heinze K.G., Kuhlemann R., Koltermann A., Schwille P. A protease assay for two-photon crosscorrelation and FRET analysis based solely on fluorescent proteins. Proc. Natl. Acad. Sci. U.S.A. 99:2002;12161-12166 Two-photon excitation is combined with FRET and cross-correlation analysis for measuring a new protease assay formed on the basis of genetically encodable intrinsically fluorescent proteins. A fusion protein consisting of eGFP and DsRed separated by a peptide with a protease cleavage site was monitored for proteolytic degradation in real-time using this combination of techniques.
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(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 12161-12166
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Kohl, T.1
Heinze, K.G.2
Kuhlemann, R.3
Koltermann, A.4
Schwille, P.5
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58
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0033573989
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Confocal fluorescence coincidence analysis: An approach to ultra high-throughput screening
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Winkler T., Kettling U., Koltermann A., Eigen M. Confocal fluorescence coincidence analysis: an approach to ultra high-throughput screening. Proc. Natl. Acad. Sci. U.S.A. 96:1999;1375-1378.
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(1999)
Proc. Natl. Acad. Sci. U.S.A.
, vol.96
, pp. 1375-1378
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Winkler, T.1
Kettling, U.2
Koltermann, A.3
Eigen, M.4
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59
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0036708472
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Two-photon fluorescence coincidence analysis: Rapid measurements of enzyme kinetics
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Heinze K.G., Rarbach M., Jahnz M., Schwille P. Two-photon fluorescence coincidence analysis: rapid measurements of enzyme kinetics. Biophys. J. 83:2002;1671-1681.
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(2002)
Biophys. J.
, vol.83
, pp. 1671-1681
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Heinze, K.G.1
Rarbach, M.2
Jahnz, M.3
Schwille, P.4
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60
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0242502951
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Triple fluorescence coincidence analysis (TFCA): Direct analysis of ternary complex formation
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in press
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Heinze KG, Jahnz M, Schwille P: Triple fluorescence coincidence analysis (TFCA): direct analysis of ternary complex formation. Biophys J 2003, in press.
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(2003)
Biophys J
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Heinze, K.G.1
Jahnz, M.2
Schwille, P.3
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