Sentence examples for microscope interfaced with from inspiring English sources

An Olympus BX61 microscope, interfaced with Soft Imaging System Colorview video camera and AnalySIS software (all Olympus Tokyo, Japan) was used.

Images of labeled sections were acquired using an Olympus Vanox-S AHBS microscope interfaced with a liquid crystal tunable filter based camera (CRI, Woburn MA, USA) from 420 nm to 720 nm at 20 nm steps.

The samples were examined using a Nikon light microscope interfaced with a spot 24-Bit Digital Color Camera.

Confocal laser scanning microscopy was performed using a Leica LCS (Leica Lasertechnik) instrument based on a Leica DM IRBE microscope interfaced with argon and helium/neon lasers emitting at 488 nm, 543 nm and 633 nm.

Briefly, the quantitative analyses were performed using an Olympus BX61 microscope interfaced with a computer and an Olympus DP71 digital camera, and the NewCAST (Computer Assisted Stereological Toolbox) software package (Olympus, Denmark).

FTIR-RM analyses were performed on the cross sections of Calc1, Calc2, Calc7, Calc8 and Calc10 using a Nic-Plan IR microscope interfaced with a Nicolet Magna-IR 550 FTIR spectrophotometer (Nicolet Instrumentations Inc., Madison, WI, USA) operated in reflectance mode, as previously described [ 14].

Images were documented with a Nikon TE-2000U inverted microscope interfacing with a Coolsnap fast cooled (ES2) digital camera at 10× (Nikon, Plan Fluor DL, NA 0.3) or 20× (Nikon, Plan Fluor ELWD, NA 0.45) objectives.

Observations were performed by two independent investigators with a Leica DMI 6000B fluorescence microscope (Leica Microsystems) equipped with the software Leica Application Suite version 1.8.0 (Leica Microsystems) or with a Leica MZ10F Modular stereo microscope interfaced to a CCD (charge-coupled device) camera and Leica Application Suite (version 1.8.0) software (Leica Microsystems).

The images of brain sections were projected from an Axioskop Zeiss light microscope using a 10× objective (Zeiss, Gottingen, Germany) through an Axiocam Zeiss high resolution digital camera attached to the microscope and interfaced with a computer.

The RoboLase microscope was interfaced with and controlled a Hamamatsu Orca-AG deep-cooled 1,344×1,024 pixel 12-bit digital CCD camera (Hamamatsu Photonics, K.K., Hamamatsu, Japan).

Immunostaining was analyzed using a fluorescence microscope (Nikon) interfaced with a digital charge-coupled device camera and an image analysis system.