Four New Systems for Optical Sectioning to Expand its Array of Fluorescence Imaging Solutions

During this year's Society for NeuroScience Annual Meeting, Carl Zeiss is introducing four new systems for Optical Sectioning to expand its array of Fluorescence Imaging Solutions.

  • Cell Observer® SD: Spinning Disk Microscope System for high-speed confocal imaging
  • LSM 700: Easy-to-use High-Performance Personal Confocal at an excellent price position
  • LSM 7 MP: Dedicated system for looking deeper with Multi Photon Imaging offering outstanding flexibility in experimental design
  • Laser TIRF 3: Reproducible and highly flexible system for Total Internal Reflection Microscopy

With these four additions and the recently introduced highly sensitive and flexible confocal Laser Scanning Microscope LSM 710 platform, Carl Zeiss is able to offer researchers the following choice of techniques for optical sectioning:

  • Total Internal Reflection (TIRF) uses an evanescent field to generate a very thin section (100 nm) of light very close to the coverslip.
  • Widefield Deconvolution takes advantage of a measured or calculated Point Spread Function to remove out of focus light.
  • Structured Illumination projects a grid into the sample and can thereby identify and remove the out-of-focus information.
  • A Spinning Disk microscope rejects out-of-focus light by inserting a rotating disk with hundreds of circular apertures into both the excitation and emission paths. A Spinning Disk system images one complete section of the field of view at a time.
  • In a Single Point Laser Scanning System, a single spot is focused into the sample and moved very rapidly across the field of view. The returning emission is filtered through a pinhole to reject the out of focus light.
  • A Line Scanner sweeps a single line of illumination across the sample and filters the returning emission through a slit aperture to reject out-of-focus light.
  • Multi-Photon microscopes (also called 2P for Two Photon or NLO for Non Linear Optics) scan a single beam across the sample, but use a pulsed infrared laser to focus the light into the sample at a density high enough so that two or more Photons excite only those fluorophores which are in the focal plane.

With this impressive choice of techniques, Carl Zeiss offers the largest family of optical sectioning microscopes on the market.

To help customers in finding the best solution for their research, Carl Zeiss MicroImaging has invested a great deal in training its expert team of Technical Sales Consultants, 3-D Imaging Specialists and Application Support Specialists. The team of experts will work together with interested scientists to determine the best solution for their application.

Tell Us What You Think

Do you have a review, update or anything you would like to add to this news story?

Leave your feedback
Your comment type
Submit

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.