Zeiss laser confocal microscopy system

Zeiss laser confocal microscopy system LSM 990

Multi functional confocal system integrating multiple imaging technologies

Zeiss laser confocal microscopy system LSM 990 combines multiple microscopy imaging techniques and is a multifunctional and excellent confocal microscopy imaging system designed specifically for life science research. The system adopts high-sensitivity detectors and multiple laser sources, which can easily achieve multi-color super-resolution 3D imaging from micrometers to tens of nanometers. Its outstanding resolution, excellent imaging depth, and ultra fast imaging speed can meet the needs of various application scenarios, providing users with excellent flexibility and imaging quality. Meanwhile, as a comprehensive multifunctional imaging platform, the LSM 990's special optical path design and powerful electronic control system endow it with excellent scalability. It can be equipped with various functional modules, enabling it to have different capabilities such as two-photon imaging, ultra-high resolution imaging, four-dimensional light field imaging, molecular dynamics detection, fluorescence lifetime imaging, and long-term cultivation of living cells, to meet the experimental needs of various samples.

lExcellent image signal-to-noise ratio

lIntegrating multiple functions into one

lThe highest resolution is up to80nm *

lKuaidaVolume imaging speed of 80 volumes/s

lThe software is efficient and easy to use, with simple operation and easy reproducibility of experimental data

lReliable measurement of molecular concentration and diffusion behavior

*The full width at half maximum of the fluorescent sphere was measured, and the result of the nanoscale ruler measurement was 90nm

lCell Biology

lDevelopmental Biology

loncology

lNeurobiology

lgene/Genetics

lbotany

lWaiting for research in the field of life sciences

useLightfield 4D performs transient volume imaging (80 volumes per second) on the beating heart of zebrafish embryos 3 days after fertilization. Provided by Stone Elworthy and Emily No ë l from the School of Biological Sciences at the University of Sheffield in the UK.

Staining of F-actin (blue) and DE Cadherin (red) in the reproductive glands of fruit flies. Image with Zeiss Airyscan 2 and then perform Joint DCV processing. Provided by T. Jacobs and AG Luschnig from the University of M ü nster in Germany

Haila cells captured in Airyscan multiplex mode, with DNA (blue), microtubules (yellow), and F-actin staining (magenta). Provided by the Max Planck Institute for Biophysical Chemistry in G ö ttingen, Germany.

Cos-7 cells, nucleus (magenta), microtubule protein (blue), actin (yellow), and mitochondria (red) are labeled. Imaging in the visible to near-infrared spectral range, spectral splitting of various signals. Samples provided by the University of Zurich in Switzerland

Blood flow direction and velocity in the blood vessels of zebrafish fry, samples collected by the Leibniz Institute for Aging Research in Germany Fritz Lippmann Institute VHopfenmüllerprovide