The Aurora CS cell sorting system delivers high-resolution capabilities at the single cell level to resolve and sort challenging cell populations, regardless of assay complexity...
The investment will be used to expand the company’s global infrastructure, sustain its growing momentum, and enable it to deliver on its flow cytometry technology platform.
During the CYTO Virtual 2020 flow cytometry conference, cell analysis instrumentation and solutions provider Cytek Biosciences unveiled its cFluor reagents.
Cytek Biosciences is supporting researchers and clinicians who are studying the effect of COVID-19 on human immune systems around the world, collaborating with over a dozen hospitals...
Cytek Biosciences has received approval from the China National Medical Products Administration for its Northern Lights flow cytometer with 24+ color capability for clinical diagnostic...
![FIGURE 1. Flow cytometry passes a stream of labeled cells in front of laser beams and an objective lens collects light emitted by the cells. In conventional systems, the laser wavelengths are matched to excite the cells’ labels, and the light collected by the objective passes through dichroic mirrors and filters to PMTs. In spectral systems, light from each of the lasers illuminates all of the labels, and the earliest of these systems featured dispersive optics that distributed fluorescence emission onto linear detector arrays. (Adapted from http://nolanlab.com/spectral-fc.html [4])](https://img.laserfocusworld.com/files/base/ebm/lfw/image/2019/02/content_dam_lfw_print_articles_2019_02_1902lfw_bg_f1.png?auto=format,compress&fit=fill&pad=5&fill-color=white&q=45&h=139&height=139&w=250&width=250 "FIGURE 1. Flow cytometry passes a stream of labeled cells in front of laser beams and an objective lens collects light emitted by the cells. In conventional systems, the laser wavelengths are matched to excite the cells’ labels, and the light collected by the objective passes through dichroic mirrors and filters to PMTs. In spectral systems, light from each of the lasers illuminates all of the labels, and the earliest of these systems featured dispersive optics that distributed fluorescence emission onto linear detector arrays. (Adapted from http://nolanlab.com/spectral-fc.html [4])")
