UMIF

UKE Microscopy Imaging Facility (DFG Research Infrastructure Portal: RI_00489)

Structured illumination microscopy (SIM)

Multicolor labeling of an eukaryotic cell.

red =actin, green = focal adhesions, blue = DAPI

Super-resolution image of detyrosinated tubulin.

Detyrosinated tubulin in neurons.

left = confocal, right = STED

Super-resolution 3D dSTORM image of microtubules

Alpha-tubulin in HeLa cells.

Color-coded z-distribution.

Combined SD-TIRF imaging of cellular vesicles

3D reconstruction of CLN3-vesicles and lysosomes in HeLa cells.

green = CLN3-GFP, red = lysosomes

Live Plasmodium berghei

P.berghei in a late stage infected HepG2 liver cell.

green = GFP-apicoplast

Confocal microscopy

Multicolor labelled cells.

JASN journal cover May 2019

The cover picture of the May 2019 issue of the Journal of the American Society of Nephrology highlights the work of J. Herwig et al. from the group of C. Meyer-Schwesinger (Institute of Cellular and Integrative Physiology, UKE). Congratulations to all the authors! In collaboration with A.V. Failla from our facility, a range of microscopes and techniques were successfully applied, such as STED super-resolution. Please find more information in our publication section. 

JASN cover May2019

TOP DOWNLOADED ARTICLE 2017-2018

Recently, one of UMIF research small report about the potential utilization of Spinning Disk-TIRF in cell biology have been reported in between the most 20 downloaded paper of journal of microscopy last year.

Thank you to all of you that have been downloading and reading this paper, and we warmly invite all the others to have a look to our works about Spinning Disk-TIRF microscopy:

Here are the paper links (please see also our publication page):

Journal of Microscopy

http://doi.org/10.1111/jmi.12626

JoVE

http://doi.org/10.3791/58756

 JoM top20

 

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