Journal: Scientific Reports

Article Title: Experimental verification of the effectiveness of neural modified sliding mode technique in multi rotor wind turbine systems

doi: 10.1038/s41598-025-94112-z

Figure Lengend Snippet: Comparison of the proposed approach with the DPC-MSMC approach.

Article Snippet: Figure represents the proposed strategy and the DPC-MSMC approach in MATLAB environment.

Techniques: Comparison

Journal: Applied Microscopy

Article Title: Multispectral intravital microscopy for simultaneous bright-field and fluorescence imaging of the microvasculature

doi: 10.1186/s42649-021-00059-6

Figure Lengend Snippet: Schematic diagram of the MSMC-23-1-A showing the bright-field and fluorescence optical paths. ( A ): The instrument includes up to seven beam splitters (BS1 - BS7), four accessory ports (A1 - A4), eight filter holders (F1 - F8), four cameras (CAM 1 - CAM 4), and two input ports (IN1, IN2). The USB 3.0 port on each camera is connected to a 4-port USB 3.0 interface card in the PC workstation. Internally, the strobe output (S1) from CAM1 is connected to the trigger inputs (T2, T3, and T4) on the other 3 cameras (CAM2, CAM3, and CAM4). ( B ): Front perspective of the MSMC-23-1-A showing C-mount ports, filter holder slots, with one slot populated with a filter holder. ( C ): Rear perspective of the MSMC-23-1-A, showing C-mount backports, USB port connections, trigger and power connectors, and switches. ( D ): Photograph of the MSIVM system with MSMC-23-1-A attached to the side port of an inverted microscope

Article Snippet: Figure shows the MSIVM system (MSMC-23-1-A, Spectral Devices Inc., London, Canada) consisting of four 2.3MP CMOS cameras (Omron Sentech, Japan, Model STC-MBS231U3V) and several beam splitters to create four separate optical arms.

Techniques: Fluorescence, Inverted Microscopy

Journal: Applied Microscopy

Article Title: Multispectral intravital microscopy for simultaneous bright-field and fluorescence imaging of the microvasculature

doi: 10.1186/s42649-021-00059-6

Figure Lengend Snippet: Fluorescent microbeads on a glass slide. Images (20X objective; 1000 × 1000 pixels; 93 μm × 93 μm) of microbeads (diameter: 1 μm) on a glass slide, observed with optical channels of the MSIVM system. Images of microbeads with emission at 645 nm are shown for the bight-field channel (400-550 nm, A ), the > 600 nm fluorescence channel ( B ), the 570/25 nm fluorescence channel ( C ), and the composite channel ( D ). Images of microbeads with emission at 560 nm are shown for the bright-field channel (400-550 nm, E ), the > 600 nm fluorescence channel ( F ), the 570/25 nm fluorescence channel ( G ), and the composite channel ( H ). Simultaneous vizualization of a mixture of two types of fluorescent microbeads (emission at 560 nm and 645 nm) on a glass slide shown for the bright-field channel ( I ), the > 600 nm fluorescence channel ( J ), the 570/25 nm fluorescencechannel ( K ), and the composite channel ( L ). Microbeads: excitation 488 nm/emission 645 nm and excitation 540 nm/emission 560 nm. Illumination wavelength range: 400–550 nm. Filters: band-pass filter (570/25 nm) and long-pass filter (600 nm). Please note that since all images are captured on monochrome cameras in the MSIVM system, no color images can be generated directly. We used image processing to add color for visualization purposes only

Article Snippet: Figure shows the MSIVM system (MSMC-23-1-A, Spectral Devices Inc., London, Canada) consisting of four 2.3MP CMOS cameras (Omron Sentech, Japan, Model STC-MBS231U3V) and several beam splitters to create four separate optical arms.

Techniques: Fluorescence, Generated

Journal: Applied Microscopy

Article Title: Multispectral intravital microscopy for simultaneous bright-field and fluorescence imaging of the microvasculature

doi: 10.1186/s42649-021-00059-6

Figure Lengend Snippet: Mixture of infused fluorescent microbeads in-vivo. ( A ): left image: Composite images of adherent infused fluorescent 1 μm microbeads, middle image : green fluorescent (560 nm) microbeads, and right image : red fluorescent microbeads (> 600 nm). Notice that the green/yellow microbeads in the composite image represent green beads visible (green channel) and, due to an optical overlap of the 560 nm emission spectrum are also visible in the red channel. In the composite picture, these appear as yellow-green, clearly distinguishable from the red fluorescent microbeads. The orange microbeads result from a positional overlap between 2 different beads (in red and green channel repsectively). ( B ), ( C ), and ( D ): Show a sequence of intravital microscopy images of a microbead moving along the vascular endothelium. Images in ( B ) and ( D ), represent the image sequences displaying the location (red circles) of the fluorescent bead visible only in image sequence ( C ) (yellow circles). Bright-field illumination wavelength range: 400–550 nm ( B ). Filters: band-pass filter: 565/24 nm ( C ) and long-pass filter: 600 nm ( D ). Microbeads: excitation 488 nm / emission 645 nm ( C ) and excitation 540 nm / emission 560 nm ( D ). Exposure: 40 ms; frame rate: 16.7 fps. Please note that since all images are captured on monochrome cameras in the MSIVM system, no color images can be generated directly. We used image processing to add color for visualization purposes only. White dotted lines indicate the approximate position of the vascular wall

Article Snippet: Figure shows the MSIVM system (MSMC-23-1-A, Spectral Devices Inc., London, Canada) consisting of four 2.3MP CMOS cameras (Omron Sentech, Japan, Model STC-MBS231U3V) and several beam splitters to create four separate optical arms.

Techniques: In Vivo, Sequencing, Intravital Microscopy, Generated

Journal: Applied Microscopy

Article Title: Multispectral intravital microscopy for simultaneous bright-field and fluorescence imaging of the microvasculature

doi: 10.1186/s42649-021-00059-6

Figure Lengend Snippet: Composite picture of a 9 s image sequence of 150 images (red and green channel). ( A ): left image: The composite image shows the path (white arrow A) of a moving microbead observed in the fluorescent > 600 nm optical channel. A group of non-moving, adherent microbeads is also visible (white arrow B); right image: Velocity of microbead A in left image of panel ( A ). The distance of the microbead was estimated in each pair of successive images. Velocity was computed by determining the traveled distance in the interframe interval. ( B ), ( C ) and ( D ): Intravital microscopy image sequence of a microbead (streak) moving in the bloodstream’s centerline. With an image exposure time of 40 ms, this free-flowing fluorescent microbead’s average velocity was 468 μm/s (range: 270–710 μm/s). Arrows in image sequences ( B and D ), displaying the location of the fluorescent bead only visible in image sequence ( C ) (yellow arrow). Bright-field illumination wavelength range: 400–550 nm ( B ). Filters: band-pass filter: 565/24 nm ( C ) and long-pass filter: 600 nm ( D ). Microbeads: excitation 488 nm / emission 645 nm and excitation 540 nm/ emission 560 nm. Exposure: 40 ms; frame rate: 16.7 fps. Please note that since all images are captured on monochrome cameras in the MSIVM system, no color images can be generated directly. We used image processing to add color for visualization purposes only. White dotted lines indicate the approximate position of the vascular wall

Article Snippet: Figure shows the MSIVM system (MSMC-23-1-A, Spectral Devices Inc., London, Canada) consisting of four 2.3MP CMOS cameras (Omron Sentech, Japan, Model STC-MBS231U3V) and several beam splitters to create four separate optical arms.

Techniques: Sequencing, Intravital Microscopy, Generated

Journal: Applied Microscopy

Article Title: Multispectral intravital microscopy for simultaneous bright-field and fluorescence imaging of the microvasculature

doi: 10.1186/s42649-021-00059-6

Figure Lengend Snippet: Composite intravital microscopy image sequence of a rolling leukocyte (red and green channel). Image sequence showing a sequence of still images ( A-D ) taken from a video sequence (see: Supplemental Video 1), revealing a rolling leukocyte with several adherent microbeads, emitting fluorescence at 600 nm (red) and 560 nm (green). With an image exposure of 40 ms, the free-flowing fluorescent microbead’s velocity ranged from 12 to 36 μm/s. Microbeads: excitation 488 nm / emission 645 nm and excitation 540 nm / emission 560 nm. Illumination wavelength range: 400–550 nm. Filters: band-pass filter (565/24 nm) and long-pass filter (600 nm). Exposure: 40 ms; frame rate: 16.7 fps. Please note that since all images are captured on monochrome cameras in the MSIVM system, no color images can be generated directly. We used image processing to add color for visualization purposes only. White dotted lines indicate the approximate position of the vascular wall

Article Snippet: Figure shows the MSIVM system (MSMC-23-1-A, Spectral Devices Inc., London, Canada) consisting of four 2.3MP CMOS cameras (Omron Sentech, Japan, Model STC-MBS231U3V) and several beam splitters to create four separate optical arms.

Techniques: Intravital Microscopy, Sequencing, Fluorescence, Generated