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Huygens STED Deconvolution Software

Specially designed for improving all STED images



STED GIF
STED microscopy has proven to be a valuable super-resolution technique for resolving objects smaller than the diffraction-limit, and Huygens leading STED deconvolution pushes this even further. All types of STED (STimulated Emission Depletion microscopy) images can be deconvolved with Huygens succesfully. Huygens unsurpassed STED deconvolution offers two-fold improvements in X, Y, and Z resolution and boosts contrast with SNRs increasing by a factor of eight. A FWHM resolution of 22nm has been achieved. More in this publication.

Image description:
Primary hippocampal neurons with cytoskeleton proteins labelled (magenta, alpha-Adducin, Abberior STAR 635P and green, ßII spectrin, Alexa 594). Imaged with Abberior Instruments’ STEDYCON and deconvolved with Huygens.


Reach 22nm Resolution

Improve image resolution, contrast and SNR effectively. Learn more: Huygens Deconvolution.


Multiple Algorithms



All Microscope Brands

All STED systems (incl. 3X) and their File Formats are supported.




Testimonials

I have been a Huygens user for 8-9 years now and the support provided by you guys are fantastic!

Dr. Priyam Banerjee, MD Anderson Cancer Center, Houston, Texas, USA.
I've been working with Huygens for couple of years now, and I can say that it's a really powerful tool. SVI have done a great job at developing a software package that is both flexible and user friendly, which is not always easy when it comes to scientific data processing. Additionally, the support I got was excellent. It is not only that SVI's team replies very fast to every inquiry, but they put consistent efforts into finding solutions for specific needs, which is really great.

Dr. Stefan Stanciu, Center for Microscopy-Microanalysis and Information Processing, University Politehnica of Bucharest, Romania.



Scientific References


The Cep57-pericentrin module organizes PCM expansion and centriole engagement.

By Watanabe K, Takao D, Ito KK, Takahashi M, Kitagawa D (2019).



Cell-cycle control of cell polarity in yeast

By Moran KD, Kang H, Araujo AV, Zyla TR, Saito K,Tsygankov D, Lew DJ (2019).



Whole-Cell, 3D, and Multicolor STED Imaging with Exchangeable Fluorophores.

By Spahn C, Grimm JB, Lavis LD, Lampe M, Heilemann M. (2019).



For more references see: Scientific References

Raw Confocal
STED + Huygens Deconvolved
Centrosome linker. U2OS cells in which the centrosome-linker-protein rootletin was immunolabelled using secondary antibodies coupled to Abberior STAR RED. Sample was prepared by R. Vlijm at MPI for Medical Research, Heidelberg, Germany. Imaged with Abberior Instruments’ STEDYCON and deconvolved with Huygens Professional.

See more: Images in the field of Cell Biology


gSTED_deconvolution_Websmaller.jpg
Gated STED single plane image and confocal data of a centriole stained with primary and secondary antibody conjugated to Chromeo488. Raw and Huygens deconvolved images are shown. The intensity profile was fitted to Lorentz distribution. Image kindly provided by Dr. Grazvydas Lukinavicius, EPFL, Lausanne, Switzerland.



See more: Images in the field of Cell Biology

Series022_gl_and_Series022_gl_deconvCMLE_stable.jpg
mipXZ_Series022_gl_raw_deconvolved.jpg
Above: Single XY plane of pulsed-STED data before (left) and after deconvolution (right) of the complete z-stack with Huygens. Structure (240 nm ring diameter) was stained with primary and secondary antibody conjugated to Alexa488. Below: Axial MIP projection of the complete STED z-stack, before (left) and after deconvolution with Huygens (right). Image kindly provided by Dr. Grazvydas Lukinavicius, EPFL, Lausanne, Switzerland.

See more: Images in the field of Cell Biology

o14_Series_website_image3.jpg
Pre-synaptic marker (Atto647n on 2nd antibody) within the neuromuscular junction of Drosophila melanogaster larvae shows holes in flower structures that were deconvolved with Huygens (picture in the middle), and that can not be identified in the raw Leica STED image (left). Raw pulsed-STED image was first stabilized and then deconvolved with Huygens. Image kindly provided by Oliver Kobler, Ulrich Thomas and Werner Zuschratter, CNI, Leibniz Institute Magdeburg, Germany.

See more: Images in the field of Neurosciences

APD__Figure.png
Confocal and STED image of chromosomes with histon proteins before and after deconvolution. Combined image of chromosomes (confocal in green) and histon protein (STED in red) image before and after deconvolution. More contrast and resolution can be observed after deconvolution of both the Leica confocal and STED channel. The image shows an enlargement of the red channel. Image kindly provided by Dr. Juraj Kabat, Biological Imaging Facility, NIH/NIAID, Bethesda, USA.

See more: Images in the field of Cell Biology

IsoSTED2
This Huygens deconvolved image shows a IsoSTED image of tubulin labelled with a small molecule probe, and imaged on an Abberior STED expert line microscope. Confocal and 3D STED images were deconvolved using Huygens software. Movie generated using Huygens MIP renderer. Image kindly provided by Dr. Grazvydas Lukinavicius, MPI for Biophysical Chemistry - Department of NanoBiophotonics, Max Planck Institute, Germany.

See more: Images in the field of Cell Biology


Available for Huygens Essential, Professional and Core

The Huygens STED optical option supports all types of STED microscopes, and can be tested with a free test license. The product is commercially available as a licensed option for Huygens Essential, Professional and Core.

Why wait? Try out this option by downloading Huygens and request a test license, or receive pricing information.

Pricing Info Request Trial