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Cell imaging using LBL-Dye M580 and LBL-Dye M717

Cellular tracers in fluorescence imaging are essential tools for studying various cellular processes, including cell migration, protein trafficking, organelle dynamics, and more...

LBL-Dye M580 and LBL-Dye M717 (compatible with super-resolution STED imaging) are two cell-permeant, photostable, and no cytotoxic cellular tracers particularly well-adapted for long-time imaging on living cells.

LBL-Dye M580

Imaging of H28-living cells stained with far-red LBL-Dye M580 (2µg/µl) in the culture medium. Images acquired by using STELLARIS8 confocal microscope (Leica Microsystems), X86 objective water immersion, WLL laser excitation 562 nm; Em 570-650 nm on HyD-S detector, Okolab chamber installed on the inverted microscope stand to keep the temperature at 37 ◦C during image acquisition.

Imaging of H28-living cells stained with far red LBL-Dye M580 (2µg/µl) after 3hrs exposure in the culture medium. Images acquired by using SP5 confocal microscope (Leica Microsystems), X63 objective oil immersion, WLL laser excitation 562nm; Em 570-650 nm. Cellular labeling is photostable, no phototoxic, allowing long time observation.

LBL-Dye M717

FireBlue LUT
Red Hot LUT
Majenta Hot LUT

Imaging of H28-living cells stained with far-red LBL-Dye M717 (5 µg/µl) in the culture medium. Images acquired by using SP5 confocal microscope (Leica Microsystems), X63 objective oil immersion, WLL laser excitation 690 nm; Em 700-730 nm. The plasma membrane and vesicles are visible on living cells and the movement of cells can be followed during few hours.

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Cellular tracers in fluorescence imaging are essential tools for studying various cellular processes, including cell migration, protein trafficking, organelle dynamics, and more...

A scratch assay is a widely used laboratory technique to study the ability of cells to migrate and close a "scratch" or "wound" made in a monolayer of cultured cells. This assay is valuable for studying cell migration, a fundamental process in tissue repair, development, and disease progression...

STED (stimulated emission depletion) microscopy offers several advantages over confocal microscopy: Higher resolution, improved contrast, faster imaging, multicolor imaging, reduced photobleaching and phototoxicity...

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