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Fv 10i confocal fluorescent microscope

Manufactured by Olympus

The FV 10i is a confocal fluorescent microscope designed for high-resolution imaging of fluorescently labeled samples. It utilizes laser-scanning technology to capture detailed, optical sections of specimens. The microscope is equipped with multiple laser lines and detectors to enable flexible fluorescence imaging.

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2 protocols using fv 10i confocal fluorescent microscope

1

Fluorescent Probe Development for Cancer Imaging

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All solvents and starting materials were purchased commercially (TCI Shanghai, J&K, Sigma-Aldrich) and used without further purification. The TCO-NHS was commercially available from Click Chemistry Tools. The GEBP11 peptide was supplied by the State Key Laboratory of Cancer Biology, the Institute of Digestive Diseases, Xijing Hospital, and the Fourth Military Medical University.
The high-performance liquid chromatography (HPLC) was used for purification of probes by on a Waters prep LC 2545 instrument. ESI-TOF-MS spectra measurements were performed by a Bruker QTOF II mass spectrometer. The imaging experiments in vitro were recorded on an Olympus FV 10i confocal fluorescent microscope. In vivo fluorescence imaging analysis was carried out in an IVIS Kinetic imaging system. The binding affinity was detected with a BD Accuri C6 flow cytometry.
A detailed description of the synthesis and characterization of all compounds can be found in the Supplementary Materials.
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2

Comprehensive Characterization of TCO-RGD

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TCO-RGD was synthesized according to our previous study43 (link). High-resolution mass spectra (HRMS) were performed on a Bruker OTOF-Q II mass spectrometer. 1H NMR spectra were recorded with a Varian 600 MHz NMR with trimethylchlorosilane as an internal standard. The fluorescence spectra were measured in an Edinburgh Instruments’ FLS1000. The imaging experiments in vitro were recorded on an Olympus FV 10i confocal fluorescent microscope, and the fluorescent signals of DAPI were recorded by blue channel (excitation 405 nm, emission 461 nm) and NIR dyes by red channel (excitation 640 nm, emission 665 nm). In vivo fluorescence imaging analysis was carried out in an IVIS Kinetic imaging system (Living Image Software version 4.5, excitation 660 nm, emission 710 nm). FACS analysis was detected with a BD Accuri C6 flow cytometry (BD CFlow Plus Software version 1.0.264.21), and fluorescent signals were recorded by FL4 channel (excitation 640 nm, emission 675 nm).
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