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(2009)
Chem. Eur. J.
, vol.15
, pp. 10762-10776
-
-
Belov, V.N.1
Bossi, M.L.2
Fölling, J.3
Boyarskiy, V.P.4
Hell, S.W.5
-
62
-
-
84957924105
-
-
For the structures of Alexa Fluor 594 diastereomers, see
-
For the structures of Alexa Fluor 594 diastereomers, see:
-
-
-
-
63
-
-
38949083506
-
-
for the preparation of this dye, see ref. [15] (compound 7)
-
A. Romieu, D. Brossard, M. Hamon, H. Outaabout, C. Portal, P.-Y. Renard, Bioconjugate Chem. 2008, 19, 279-289; for the preparation of this dye, see ref. [15] (compound 7).
-
(2008)
Bioconjugate Chem.
, vol.19
, pp. 279-289
-
-
Romieu, A.1
Brossard, D.2
Hamon, M.3
Outaabout, H.4
Portal, C.5
Renard, P.-Y.6
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64
-
-
84870927539
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-
S. Nizamov, K. I. Willig, M. V. Sednev, V. N. Belov, S. W. Hell, Chem. Eur. J. 2012, 18, 16339-16348.
-
(2012)
Chem. Eur. J.
, vol.18
, pp. 16339-16348
-
-
Nizamov, S.1
Willig, K.I.2
Sednev, M.V.3
Belov, V.N.4
Hell, S.W.5
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65
-
-
84957924106
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-
Details of preparation, properties, and the use of the "universal hydrophlilizer" 11 will be reported later
-
Details of preparation, properties, and the use of the "universal hydrophlilizer" 11 will be reported later.
-
-
-
-
66
-
-
84957924107
-
-
Methanol was used as a solvent for the model compounds in the preparative photolysis experiments, from which the fluorescent homologues (3 a -Y,Me- 3 e -Y,Me) of the parent Rhodamines NN and the non-emitting ("dark") products (4 a -Y- 4 e -Y) were isolated (see Scheme 1 and the Supporting Information for details).
-
Methanol was used as a solvent for the model compounds in the preparative photolysis experiments, from which the fluorescent homologues (3 a -Y,Me- 3 e -Y,Me) of the parent Rhodamines NN and the non-emitting ("dark") products (4 a -Y- 4 e -Y) were isolated (see Scheme 1 and the Supporting Information for details).
-
-
-
-
69
-
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12744269340
-
-
H. J. Kuhn, S. E. Braslavsky, R. Schmidt, Pure Appl. Chem. 2004, 76, 2105-2146.
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(2004)
Pure Appl. Chem.
, vol.76
, pp. 2105-2146
-
-
Kuhn, H.J.1
Braslavsky, S.E.2
Schmidt, R.3
-
70
-
-
84957924108
-
-
Compare with the values for the photactivation (uncaging) quantum yields reported in references [4a], [5], [6], [8b], [9a], [13], and in the following publications
-
Compare with the values for the photactivation (uncaging) quantum yields reported in references [4a], [5], [6], [8b], [9a], [13], and in the following publications:
-
-
-
-
71
-
-
77950261891
-
-
W. Lin, L. Long, W. Tan, B. Chen, L. Yuan, Chem. Eur. J. 2010, 16, 3914-3917;
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 3914-3917
-
-
Lin, W.1
Long, L.2
Tan, W.3
Chen, B.4
Yuan, L.5
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72
-
-
4544259296
-
-
V. Hagen, J. Bendig, S. Frings, T. Eckardt, S. Helm, D. Reuter, U. B. Kaupp, Angew. Chem. 2001, 113, 1077-1080;
-
(2001)
Angew. Chem.
, vol.113
, pp. 1077-1080
-
-
Hagen, V.1
Bendig, J.2
Frings, S.3
Eckardt, T.4
Helm, S.5
Reuter, D.6
Kaupp, U.B.7
-
73
-
-
0035857544
-
-
Angew. Chem. Int. Ed. 2001, 40, 1045-1048;
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 1045-1048
-
-
-
74
-
-
84886848240
-
-
J. del Mármol, O. Filevich, R. Etchenique, Anal. Chem. 2010, 82, 6259-6264;
-
(2010)
Anal. Chem.
, vol.82
, pp. 6259-6264
-
-
Del Mármol, J.1
Filevich, O.2
Etchenique, R.3
-
76
-
-
84957924109
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-
For labeling protocols, see, for example
-
For labeling protocols, see, for example: http://www.abberior.com/fileadmin/user-upload/documents/Downloads/Application-Notes/20120316-Labeling-Protocol.pdf;
-
-
-
-
77
-
-
84957924110
-
-
In the case of the lipophilic NHS esters derived from the caged dyes 2 a, 2 bc, 2 c, and KK1012, amino-reactive dye (0.2 mg) dissolved in dry DMF (40 μL) was added slowly to the stirred and buffered (pH≈8.5) protein solution (1 mg of a secondary antibody in 1 mL buffer), followed by incubation and common isolation procedures (gel-filtration, evaluation of protein concentrations, etc.). More hydrophilic caged dyes 2 d,Na and 10 require less DMF
-
https://www.atto-tec.com/fileadmin/user-upload/Katalog-Flyer-Support/Procedures.pdf. In the case of the lipophilic NHS esters derived from the caged dyes 2 a, 2 bc, 2 c, and KK1012, amino-reactive dye (0.2 mg) dissolved in dry DMF (40 μL) was added slowly to the stirred and buffered (pH≈8.5) protein solution (1 mg of a secondary antibody in 1 mL buffer), followed by incubation and common isolation procedures (gel-filtration, evaluation of protein concentrations, etc.). More hydrophilic caged dyes 2 d,Na and 10 require less DMF;
-
-
-
-
78
-
-
84957924111
-
-
value provided by the producer
-
value provided by the producer (https://www.atto-tec.com);
-
-
-
-
80
-
-
56149115286
-
-
J. Fölling, M. L. Bossi, H. Bock, R. Medda, C. A. Wurm, B. Hein, S. Jakobs, C. Eggeling, S. W. Hell, Nat. Methods 2008, 5, 943-945.
-
(2008)
Nat. Methods
, vol.5
, pp. 943-945
-
-
Fölling, J.1
Bossi, M.L.2
Bock, H.3
Medda, R.4
Wurm, C.A.5
Hein, B.6
Jakobs, S.7
Eggeling, C.8
Hell, S.W.9
-
81
-
-
84957924112
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-
For further examples, see
-
For further examples, see:
-
-
-
-
82
-
-
84894656819
-
-
4159
-
D. Eggert, M. Naumann, R. Reimer, C. A. Voigt, Sci. Rep. 2014, 4, 4159, DOI: 10.1038/srep04159
-
(2014)
Sci. Rep.
, vol.4
-
-
Eggert, D.1
Naumann, M.2
Reimer, R.3
Voigt, C.A.4
-
83
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84957924113
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-
microscopic images obtained with Abberior Cage dyes (500, 532, 552, 590, 635): www.abberior.com
-
microscopic images obtained with Abberior Cage dyes (500, 532, 552, 590, 635): www.abberior.com;
-
-
-
-
84
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84957924114
-
-
for spectral properties of the (uncaged) dyes that can be used in STED microscopy, see: (Eds.: E. F. Fornasiero, S. Rizzoli), Superresolution Microsopy Techniques in Neurosciences, Humana Press, New York, .
-
for spectral properties of the (uncaged) dyes that can be used in STED microscopy, see: Springer Protocols. (Eds.:, E. F. Fornasiero, S. Rizzoli,), Superresolution Microsopy Techniques in Neurosciences, Humana Press, New York, 2014, pp. 354-356.
-
(2014)
Springer Protocols.
, pp. 354-356
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-
-
85
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36949010308
-
-
V. Westphal, M. A. Lauterbach, A. DiNicola, S. W. Hell, New J. Phys. 2007, 9, 435-445.
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(2007)
New J. Phys.
, vol.9
, pp. 435-445
-
-
Westphal, V.1
Lauterbach, M.A.2
Dinicola, A.3
Hell, S.W.4
-
86
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23444448243
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-
T. Gronemeyer, G. Godin, K. Johnsson, Curr. Opin. Biotechnol. 2005, 16, 453-458.
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(2005)
Curr. Opin. Biotechnol.
, vol.16
, pp. 453-458
-
-
Gronemeyer, T.1
Godin, G.2
Johnsson, K.3
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87
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84957924115
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For reviews, see
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For reviews, see:
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-
-
-
88
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77952335621
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-
(Eds.: A. Gräslund, R. Rigler, J. Widengren), Springer, Berlin
-
S. W. Hell, Far-Field Optical Nanoscopy; in: Single Molecule Spectroscopy in Chemistry, Physics and Biology (Eds.:, A. Gräslund, R. Rigler, J. Widengren,), Springer, Berlin, 2009, pp. 365-398;
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(2009)
Far-Field Optical Nanoscopy; In: Single Molecule Spectroscopy in Chemistry, Physics and Biology
, pp. 365-398
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Hell, S.W.1
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89
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34249945258
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-
S. W. Hell, Science 2007, 316, 1153-1158;
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(2007)
Science
, vol.316
, pp. 1153-1158
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Hell, S.W.1
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94
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67650762824
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B. Huang, M. Bates, X. Zhuang, Annu. Rev. Biochem. 2009, 78, 993-1016;
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(2009)
Annu. Rev. Biochem.
, vol.78
, pp. 993-1016
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-
Huang, B.1
Bates, M.2
Zhuang, X.3
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95
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78650512639
-
-
B. Huang, H. Babcock, X. Zhuang, Cell 2010, 143, 1047-1058;
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(2010)
Cell
, vol.143
, pp. 1047-1058
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Huang, B.1
Babcock, H.2
Zhuang, X.3
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