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List of parts and materials needed to build the proposed LED lamp.

Journal: Applications in Plant Sciences

Article Title: An open‐source LED lamp for use with the LI‐6800 photosynthesis system

doi: 10.1002/aps3.11622

Figure Lengend Snippet: List of parts and materials needed to build the proposed LED lamp.

Article Snippet: COB‐LED holder , Molex, Lisle, Illinois, USA , 180555‐0002 , 1.

Techniques: Adhesive, Blocking Assay

Journal: HardwareX

Article Title: Open source timed pressure control hardware and software for delivery of air mediated distensions in animal models

doi: 10.1016/j.ohx.2022.e00271

Figure Lengend Snippet:

Article Snippet: 5 mm Chromed Metal Narrow Bevel LED Holder , 2176 , 3 , $0.59 , $1.77 , Adafruit , Chromed Metal and Plastic.

Techniques: Control

Microscopy system and example images of PBMC from a healthy control. ( A ) Combined automated darkfield and epi-fluorescence microscope developed for the project. ( B ) Maximum-intensity projection of the z-stack darkfield image of a field of view. Some cells show PNPs bound to them. ( C ) First fluorescent channel showing all PBMC in green (CD45) and B cells in blue (CD19). ( D ) Second fluorescent channel showing monocytes in green (CD14) and NK cells in orange (CD56). ( E ) Third fluorescent channel showing NK cells in orange (CD56) and T cells in red (CD3). ( F ) Fourth fluorescent channel showing T cells in red (CD3). ( G ) Representative slices of the z-stack of the monocyte highlighted in B. Please observe how PNPs are visible on the planes of the cell that are above (top) and below (bottom) its equatorial plane (middle), located in the center of the inset. This is due to the high brightness of the plasmonic nanoparticles and the transparency of the cells under darkfield. Numbers indicate the order of the image in the z-stack. ( H ) Composite image showing the darkfield maximum-intensity projection and 4-channel fluorescence of example cells of different lineages. Please observe how, for these examples, the monocyte exhibits high CA125 binding, the B-cell medium CA125 binding and other cell classes show no binding.

Journal: Cancers

Article Title: Characterization of Cell-Bound CA125 on Immune Cell Subtypes of Ovarian Cancer Patients Using a Novel Imaging Platform

doi: 10.3390/cancers13092072

Figure Lengend Snippet: Microscopy system and example images of PBMC from a healthy control. ( A ) Combined automated darkfield and epi-fluorescence microscope developed for the project. ( B ) Maximum-intensity projection of the z-stack darkfield image of a field of view. Some cells show PNPs bound to them. ( C ) First fluorescent channel showing all PBMC in green (CD45) and B cells in blue (CD19). ( D ) Second fluorescent channel showing monocytes in green (CD14) and NK cells in orange (CD56). ( E ) Third fluorescent channel showing NK cells in orange (CD56) and T cells in red (CD3). ( F ) Fourth fluorescent channel showing T cells in red (CD3). ( G ) Representative slices of the z-stack of the monocyte highlighted in B. Please observe how PNPs are visible on the planes of the cell that are above (top) and below (bottom) its equatorial plane (middle), located in the center of the inset. This is due to the high brightness of the plasmonic nanoparticles and the transparency of the cells under darkfield. Numbers indicate the order of the image in the z-stack. ( H ) Composite image showing the darkfield maximum-intensity projection and 4-channel fluorescence of example cells of different lineages. Please observe how, for these examples, the monocyte exhibits high CA125 binding, the B-cell medium CA125 binding and other cell classes show no binding.

Article Snippet: The microscope was based upon Cerna microscope components (Thorlabs), consisting of a darkfield slide holder equipped with side illumination RGB and White LEDs, an EPI-fluorescence imaging unit, a laser-based autofocusing unit and a SCMOS 8 Mp color camera (4096 × 2678 pixels) (Thorlabs CS985CU).

Techniques: Microscopy, Control, Fluorescence, Binding Assay