Abstract:
A method for driving an acousto-optic element with an acousto-optic crystal and a piezoelectric transducer for setting the acousto-optic crystal in mechanical vibration includes driving the piezoelectric transducer with a drive signal with at least one drive frequency. The at least one drive frequency in alternation takes on a plurality of different values around a center frequency during a passage of a mechanical vibrational wave through the acousto-optic crystal, such that a grating that is produced owing to density fluctuations in the acousto-optic crystal exhibits different grating spacings at the same time.
Abstract:
An electric circuit for driving an acousto-optic crystal includes a piezoelectric converter configured to drive the acousto-optic crystal to vibrate mechanically. A signaling cable is configured to conduct a first electrical alternating-current signal and a second electrical signal. The electric circuit further includes a first frequency-separating filter and a second frequency-separating filter, each of the frequency-separating filters having an input, a high-frequency output and a low-frequency output. The input of the first frequency-separating filter and the input of the second frequency-separating filter is connected to the signaling cable, and the high-frequency output of the second frequency-separating filter is connected to the piezoelectric converter.
Abstract:
A microscope, in particular a confocal microscope, has one or more lasers for generating an illumination light for a sample and has a detection device for detected signals from the sample. The detection device includes multiple adjustable spectral detection channels for the detection of predefinable different wavelength regions, and is configured and refined in the interest of particularly versatile utilization in consideration of a wide variety of phenomena, with particularly good separation of the phenomena in the context of investigation, in such a way that multiple temporal detection windows are respectively settable for the spectral detection channels.
Abstract:
The invention relates to a method for investigating a sample with regard to the lifetime of an excited state, in particular a fluorescence lifetime, and/or with regard to a property of a sample which is correlated with a lifetime of an excited state, in particular with a fluorescence lifetime, a sample region being illuminated with a sequence of excitation light pulses. The method is characterized in that the light quantity and/or number of photons of the detected light, in particular fluorescent light, proceeding from the sample region is measured temporally between the excitation light pulses exclusively within a detection time window in each case, at least two detection time windows having different temporal lengths.
Abstract:
A microscope, in particular a confocal microscope, has one or more lasers for generating an illumination light for a sample and has a detection device for detected signals from the sample. The detection device includes multiple adjustable spectral detection channels for the detection of predefinable different wavelength regions, and is configured and refined in the interest of particularly versatile utilization in consideration of a wide variety of phenomena, with particularly good separation of the phenomena in the context of investigation, in such a way that multiple temporal detection windows are respectively settable for the spectral detection channels.
Abstract:
The present invention relates to a confocal laser scanning microscope (100) having an illumination device (1) that comprises a laser light source (41) that is configured to illuminate a sample (25), and a control application circuit (40) for the laser light source (1) which is configured to output a pulsed control application signal (48) in order to supply the laser light source (41), the control application circuit (40) being configured so that it determines both a pulse amplitude (A) and a pulse width (W) of at least one pulse of the pulsed control application signal (48) as a function of at least one input variable (S).
Abstract:
A method for counting photons using a photomultiplier includes obtaining a measurement signal from a raw signal produced by the photomultiplier by correcting the raw signal for a noise signal and/or an offset, wherein an incident photon produces a pulse in the raw signal. The measurement signal is integrated over time to form an analog integrated measurement signal. A number of photons that are incident in the photomultiplier is ascertained by comparing a value of the analog integrated measurement signal to an integral proportionality value which corresponds to a specific number of photons incident in the photomultiplier.
Abstract:
The present invention relates to a confocal laser scanning microscope (100) having an illumination device (1) that comprises a laser light source (41) that is configured to illuminate a sample (25), and a control application circuit (40) for the laser light source (1) which is configured to output a pulsed control application signal (48) in order to supply the laser light source (41), the control application circuit (40) being configured so that it determines both a pulse amplitude (A) and a pulse width (W) of at least one pulse of the pulsed control application signal (48) as a function of at least one input variable (S).
Abstract:
An electric circuit for driving an acousto-optic crystal includes a piezoelectric converter configured to drive the acousto-optic crystal to vibrate mechanically. A signaling cable is configured to conduct a first electrical alternating-current signal and a second electrical signal. The electric circuit further includes a first frequency-separating filter and a second frequency-separating filter, each of the frequency-separating filters having an input, a high-frequency output and a low-frequency output. The input of the first frequency-separating filter and the input of the second frequency-separating filter is connected to the signaling cable, and the high-frequency output of the second frequency-separating filter is connected to the piezoelectric converter.
Abstract:
A fluorescence-lifetime imaging microscopy method with time-correlated single-photon counting includes using excitation light pulses separated in each case by a measurement interval to excite a sample to emit fluorescence photons. A detector signal that represents the captured fluorescence photons is generated. Detection times are determined based on the detector signal. Imaging is performed based on the detection times. The detection times of all captured fluorescence photons are compiled in a first data memory, common to a plurality of image pixels. The detection times of only those fluorescence photons which were captured in a predetermined number within the respective measurement intervals are compiled in a second data memory, common to the same plurality of image pixels. The detection times compiled in the data memories are combined within a calculation step. The results of the calculation step are stored in a third data memory.