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fluorescence_correlation_spectroscopy-_a_short_introduction @general
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oTime FCS Correlation}} ====== Introduction to Fluorescence Correlation Spectroscopy ====== ===== General Background ===== Fluorescence Correlation Spectroscopy (FCS) is founded on the analysis of the fluctuations of the fluorescence intensity detected from a given system. FCS was ... ves obtained by measuring the fluctuations of the fluorescence intensity of a population of freely diffusing mol
software
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ite for acquisition and analysis of time resolved fluorescence data. SymPhoTime features a powerful scripting la... ed by the [[http://www.lfd.uci.edu|Laboratory for Fluorescence Dynamics]] to analyse FLIM data via the Phasor ap... an open-source Python library for the analysis of fluorescence lifetime and hyperspectral images using the phaso... s a Python GUI for interactive phasor analysis of Fluorescence Lifetime Microscopy (FLIM) data [[https://github.
video_tutorials
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found on youtube that explain the basics of [[wp>fluorescence]], [[glossary:fluorescence lifetime]] and its applications. ==== Fluorescence and Fluorescence Microscopy ==== Fluorescence is the emission of light by a substance that has absorbed light o
how_to_measure_the_instrument_response_function_irf @howto
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t rate is much lower than the count rate during a fluorescence decay measurement. Diluting the scattering soluti... es. In order to avoid signal contamination by any fluorescence, the water must be very pure. ===== Using samp... lution. The solution is to acquire the IRF at the fluorescence wavelength, or at least spectrally closer to the fluorescence emission wavelength. ==== General recipe ====
using_the_flcs_script_for_spectral_crosstalk_removal_via_flccs @howto
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l shows step-by-step, how to calculate a spectral fluorescence lifetime cross-correlation (FLCCS) curve from a m... }} ===== Background Information ===== **Note:** Fluorescence Cross-Correlation Spectroscopy (FCCS) is a method... ission properties but they can also vary in their fluorescence lifetime.\\ To quantify the cross-correlation sig... ited with a pulsed and the other with a cw laser, fluorescence lifetime cross-correlation (FLCCS) is an ideal to
diamond_nv_centers @howto
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Emission filters therefor should be 650LP. ==== Fluorescence Lifetime ==== *Fluorescence Lifetime is approx. 12ns. ===== Measuring NV centers ===== [{{ howto:jablon... he nitrogene-vacancy in a diamond lattice. Bright fluorescence corresponds to the ^3E→^3A (m_s=0) transition}}] ... 0MHz - for finding the centers, later 10MHz (12ns fluorescence lifetime)) *excitation power: >7000 a.u. @ 4
some_origins_of_multiexponetial_decays_for_single_dyes
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multiexponetial decays for pure dyes ====== The fluorescence lifetime of a dye measured with a TCSPC spectrome... product of the rotation correlation time and the fluorescence lifetime, divided by their sum). And they also kn... B) absorb may lead to biexponential decays if the fluorescence of both compounds is observed at the same wavelen... excited-state reaction relative the the original fluorescence lifetime, the observed decay time measured with a
measurement_hardware_instrumentation
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rumentation ====== ===== Spectroscopy ===== [[Fluorescence Lifetime Measurements using the FluoTime 300|Fluorescence Lifetime Measurements]] [[Fluorescence Lifetime Measurements using the FluoTime 300#Time-Resolved Fluorescence Anisotropy Measurements]] [[Fluorescence Lifetim
fcs @glossary
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====== Fluorescence Correlation Spectroscopy (FCS) ====== Fluorescence correlation spectroscopy (FCS) is a correlation analysis of fluctuation of the fluorescence intensity. The analysis provides parameters of th... (molecules) in solution. In this application, the fluorescence emitted from a very tiny space in solution contai
calculate_ratiometric_single_pair_fret_distributions @howto
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itions. The script requires a spectrally resolved fluorescence time trace. As a result, the distribution of FRET... * The script requires a time trace containing the fluorescence of two spectrally separated channels, one channel mainly detecting the fluorescence of the donor dye and the other channel detecting mainly the fluorescence of the acceptor dye.\\ The time traces can be acq
calculate_ratiometric_single_pair_fret_distributions_using_the_pie-fret_script @howto
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(PIE). The script requires a spectrally resolved fluorescence time trace, in which donor and acceptor have been... * The script requires a time trace containing the fluorescence of two spectrally separated channels, one channel mainly detecting the fluorescence of the donor dye and the other channel detecting mainly the fluorescence of the acceptor dye.\\ The time traces can be acq
basics
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{{tag> basics introduction FCS fluorescence microscopy objective resolution NA tutorials}} ====== Basics ====== * [[video_tutorials|Fluorescence and Fluorescence Microscopy by Nico Stuurman]] * [[video_tutorials#Kurt Thorn: Optical Sectioning and Confoc... ory, simulator and assessment.]] * [[general:fluorescence_correlation_spectroscopy-_a_short_introduction |
fluorescence_lifetime_measurements_using_the_fluotime_300
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300}} ~~TOC~~ ====== FluoTime 300 ====== ===== Fluorescence Lifetime Measurements ===== {{ youtube>X9ogeveN-MU?large }} Fluorescence lifetime measurements on the [[products:FluoTime3... ation wizards of the system. ===== Time-Resolved Fluorescence Anisotropy Measurements ===== {{ youtube>mo9HtWSiMb8?large }} Time-Resolved Fluorescence Anisotropy measurements on the FluoTime 300 from
microtime @products
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===== MicroTime 100 ===== Upright Time-resolved Fluorescence Microscope * Complete system with laser combini... ion: [[http://www.picoquant.com/products/category/fluorescence-microscopes/microtime-100-upright-time-resolved-fluorescence-microscope|MicroTime 100]] ===== MicroTime 200 ===== Time-resolved confocal fluorescence microscope with unique single molecule sensitivit
using_the_anisotropy_image_script @howto
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early polarized excitation and two detectors. The fluorescence should have been splitted with a polarizing beams... etectors. Consequently, one detector receives the fluorescence with a polarization parallel to the excitation li... sis and processing options. - **Upper center:** Fluorescence intensity image, displayed in false color scale. The perpendicular and parallel fluorescence intensities measured with the two detectors are d
applications
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start
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antibunching_measurements @howto
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calculate_fccs_trace_with_the_grouped_fcs_script @howto
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flim_fret_calculation_for_multi_exponential_donors @howto
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separation_of_2_species_with @howto
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using_the_antibunching_script @howto
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pile-up_effect @glossary
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lifetime-fitting_using_the_flim_script @howto
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flim @glossary
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fluorescence_lifetime @glossary
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intensity_time_trace_analysis @howto
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lifetime_fitting_using_the_flim_analysis @howto
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roi_fitting_using_the_flim_script @howto
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howto @howto
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update @howto
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fluofit @software
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pycorrfit @software
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lsm710
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community_news @general
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convolution @glossary
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mcs @glossary
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support_plane_analysis @glossary
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t2-mode @glossary
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t3-mode @glossary
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tcspc @glossary
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2ffcs @howto
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calculate_and_fit_fcs_traces_with_the_fcs_script @howto
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mt200fcs @howto
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pattern_matching @howto
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phasor_analysis @howto
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symphotime_tips_and_tricks @howto
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flimfit @software
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symphotime64 @software
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