Comparison and accuracy of methods to determine the confocal volume for quantitative fluorescence correlation spectroscopy

2008 ◽  
Vol 232 (2) ◽  
pp. 343-352 ◽  
Author(s):  
S. RÜTTINGER ◽  
V. BUSCHMANN ◽  
B. KRÄMER ◽  
R. ERDMANN ◽  
R. MACDONALD ◽  
...  
2018 ◽  
Author(s):  
B Sahoo ◽  
TB Sil ◽  
B Karmakar ◽  
K Garai

ABSTRACTWe have developed a fluorescence correlation spectroscopy (FCS) setup for performing single molecule measurements on samples inside regular cuvettes. We built this by using an Extra Long Working Distance (ELWD), 0.7 NA, air objective with working distance > 1.8 mm. We have achieved counts per molecule > 44 kHz, diffusion time < 64 μs for rhodamine B in aqueous buffer and a confocal volume < 2 fl. The cuvette-FCS can be used for measurements over a wide range of temperature that is beyond the range permitted in the microscope-based FCS. Finally, we demonstrate that cuvette-FCS can be coupled to automatic titrators to study urea dependent unfolding of proteins with unprecedented accuracy. The ease of use and compatibility with various accessories will enable applications of cuvette-FCS in the experiments that are regularly performed in fluorimeters but are generally avoided in microscope-based FCS.


2016 ◽  
Vol 18 (18) ◽  
pp. 12877-12885 ◽  
Author(s):  
A. Wolf ◽  
C. Schneider ◽  
T.-Y. Kim ◽  
K. Kirchberg ◽  
P. Volz ◽  
...  

Fluorescence correlation spectroscopy (FCS) is a single molecule based technique to temporally resolve rate-dependent processes by correlating the fluorescence fluctuations of individual molecules traversing through a confocal volume.


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