Optical microscopy has historically played an important role in life-science discovery. Advances in imaging technology are rapidly expanding the boundaries of what is possible, allowing for studies of live cells with unprecedented spatio-temporal resolution and the extraction of diverse biophysical parameters intrinsic to the processes of life.
The Advanced Microscopy Facility offers a range of cutting-edge, novel and custom optical microscopy techniques, along with associated expertise and assistance, for life science researchers.
Interested in using one of our techniques? Need additional information? Got a specific project question?
Following discussion and planning of your project, expert facility staff perform the agreed experiments together with you and assist you with data analysis and interpretation as required for your project. An hourly fee per staff-hour and instrument-hour is charged.
For longer-term projects or if you are planning to use an instrument extensively/for several different projects, it may often be desirable to operate the instrument independent of facility staff availability. In this case, training on an instrument by an expert staff member is possibleTraining times will depend on the technique and instrument (estimates provided beforehand). Independent usage on completion of training at trainers’ discretion.
Instruments may be reserved via our online booking system. We currently have a 24 hr cancellation policy, after which the cost of the respective booked instrument-hours will be charged. Independent operation is charged at an instrument dependent hourly rate.
Consulting is provided free of charge if it is tied to the usage or potential usage of an instrument/technique at the facility. General consulting on microscopy related topics is provided at an hourly rate subject to staff availability.
To assure funding bodies that we are a worthwhile investment, please remember to acknowledge the facility in all dissemination activities (publications, presentations, etc.) that include data obtained using one of our instruments preferably as follows:
“We acknowledge the Advanced Microscopy Facility of the Vienna BioCenter Core Facilities, member of the Vienna BioCenter Austria, for [service+description of microscope]“.
If a member/members of the facility have contributed scientifically/intellectually to the results or the process of obtaining them, and you would like to acknowledge them as co-authors, please contact us to assure that all relevant funding sources are correctly acknowledged.
β-Catenin–dependent mechanotransduction dates back to the common ancestor of Cnidaria and Bilateria.
Pukhlyakova E, Aman AJ, Elsayad K, Technau U. Proceedings of the National Academy of Sciences, 115(24), 6231-6236.
Axicon-based Bessel beams for flat-field illumination in total internal reflection fluorescence microscopy.
Schreiber B, Elsayad K, Heinze KG. Optics Letters 42(19):3880-3883 (2017)
A novel non-canonical PIP-box mediates PARG interaction with PCNA
Kaufmann T, Grishkovskaya I, Polyansky AA, Kostrhon S, Kukolj E, Olek KM, Herbert S, Beltzung E, Mechtler K, Peterbauer T, Gotzmann J, Zhang L, Hartl M, Zagrovic B, Elsayad K, Djinovic-Carugo K, Slade D. July 2017 Nucleic Acids Res gkx604
Fluorescence Excitation, Decay, and Energy Transfer in the Vicinity of Thin Dielectric/Metal/Dielectric Layers near Their Surface Plasmon Polariton Cutoff Frequency
Elsayad K and Heinze KG. Chapter 6, Page 111 in "Surface Plasmon Enhanced, Coupled and Controlled Fluorescence" (1st Edition, Edited by C. Geddes).
Mapping the subcellular mechanical properties of live cells in tissues with fluorescence emission–Brillouin imaging
Elsayad K, Werner S, Gallemí M, Kong J, Sánchez Guajardo ES, Zhang L, Jaillais Y, Greb T, Belkhadir Y, Sci. Signal. 05 Jul 2016: Vol. 9, Issue 435, pp. rs5
The expression of tubb2b undergoes a developmental transition in murine cortical neurons
Breuss M, Morandell J, Nimpf S, Gstrein T, Lauwers M, Hochstoeger T, Braun A, Chan K, Sánchez Guajardo ES, Zhang L, Suplata M, Heinze KG, Elsayad K, Keays DA, 2015 Journal of Comparative Neurology Volume 523, Issue 15, pages 2161–2186, 15 October 2015
Membrane Protein Localization by SpecON.
Heinze KG, Elsayad K. Imaging & Microscopy16:23
Mal3, the Schizosaccharomyces pombe homolog of EB1, is required for karyogamy and for promoting oscillatory nuclear movement during meiosis
Polakova S, Benko Z, Zhang L, Gregan J Cell Cycle. 13:72
Spectrally coded optical nanosectioning (SpecON) with biocompatible metal–dielectric-coated substrates.
Elsayad K, Urich A, Tan PS, Nemethova M, Small JV, Unterrainer K, Heinze KG. Proc. Nat. Acad. Sci USA 110:20069
Differential Action of Reelin on Oligomerization of ApoER2 and VLDL Receptor in HEK293 Cells Assessed by Time-Resolved Anisotropy and Fluorescence Lifetime Imaging Microscopy.
Dlugosz P, Tresky R, Nimpf J, Front. Mol. Neurosci., 26 Feb 2019
p62 filaments capture and present ubiquitinated cargos for autophagy
Zaffagnini G, Savova A, Danieli A, Romanov J, Tremel S, Ebner M, Peterbauer T, Sztacho M, Trapannone R, Tarafder AK, Sachse C, Martens S. The EMBO journal, e98308.
Host-Polarized Cell Growth in Animal Symbionts.
Pende N, Wang J, Weber PM, Verheul J, Kuru E, Rittmann SRK, Leisch N, VanNieuwenhze MS, Brun YV, den Blaauwen T, Bulgheresi S.Current Biology, 28(7), 1039-1051.