A fluorescence super-resolution microscopy device and method based on virtual wave vector modulation
A virtual wave vector and super-resolution technology, applied in the field of confocal microscopy, which can solve the problems of limited fluorescent labeling substances, noise and aberration, and low optical sectioning ability.
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Embodiment 1
[0081] Such as figure 1 As shown, a fluorescent super-resolution microscopy device based on virtual wave vector modulation that scans the sample by controlling the scanning galvanometer and the z-axis translation stage, including a laser 1, a lens 2, a mirror 3, a dichroic mirror 4, and a vibrating Mirror scanning system 5, scanning mirror 6, reflecting mirror 7, field mirror 8, microscope objective lens 9, sample 10, z-axis piezoelectric platform 15, filter 11, magnifying imaging system 12, rectangular detector array 13, computer 14.
[0082] use figure 1 The shown setup realizes the two-color microscopy method based on virtual wave vector modulation for the sample, and the process is as follows:
[0083] (1) The laser 1 emits an excitation beam, which is first collimated by the lens 2, reflected by the first mirror 3, reflected by the dichromatic mirror 4, and enters the scanning galvanometer system 5; the excitation light guided by the scanning galvanometer system 5 pass...
Embodiment 2
[0089] Such as image 3 As shown, a fluorescent super-resolution microscopy device based on virtual wave vector modulation that scans samples by controlling a three-dimensional translation stage, including a laser 1, a lens 2, a mirror 3, a dichromatic mirror 4, a scanning mirror 6, and a mirror 7. Field lens 8, microscope objective lens 9, sample 10, three-dimensional translation stage 16, filter plate 11, magnifying imaging system 12, honeycomb coal-shaped detector array 13, computer 14.
[0090] use image 3 The shown setup realizes the two-color microscopy method based on virtual wave vector modulation for the sample, and the process is as follows:
[0091](1) The laser 1 sends out the exciting light beam, which is first collimated by the lens 2, reflected by the first reflector 3, reflected by the dichromatic mirror 4, and forms a scanning area on the rear focal plane after the scanning mirror 6; the field lens 8 and The microscope objective lens 9 jointly forms an imag...
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