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LiMiTec

Light Microscopy Technology Platform of Bielefeld University

© Universität Bielefeld

Instruments

Confocal Microscopes

Inverted confocal laser scanning microscope & FLIM & FCS (W0-226)

  • Laser lines: 405 nm, pulsed WLL 440 - 790 nm
  • Detectors: 2 HyD S, 2 HyD X, 1 HyD R
  • Optional: temperature-controlled stage with CO2-incubation
  • Software: Leica LAS X

Phone at microscope: 5690

Contact: Thorsten Seidel

Inverted confocal laser scanning microscope & FCS (W01)

  • Laser lines: 405 nm, 458 nm, 488 nm, 514 nm, 561 nm, 633 nm
  • Detectors: 2 photomultipliers, 32-ch GaAsp-detector
  • Optional: temperature-controlled stage with CO2-incubation
  • Software: Zeiss ZEN 2011

Phone at microscope: 5615

Contact: Thorsten Seidel

Inverted confocal laser scanning microscope (Building R1-D2)

  • Laser lines: 405 nm, 488 nm, 561 nm, 640 nm
  • 2 GaAsp Detectors
  • Airyscan Detector
  • Temperature-controlled with CO2-incubation
  • Software: Zeiss ZEN Blue

Phone at microscope: xxxx

Contact: Barbara Biermann

Inverted Stand Nikon Ti2E with Crest Spinning Disc (Building R1-D2)

  • Objectives: 10x/0.45, 20x/0.8, 40x/0.95, 40x/1.15, 60x/1.42
  • Laser lines: 405 nm, 446 nm, 476 nm, 518 nm, 546 nm, 637 nm, 748 nm
  • Camera: Photometrix Kinetics
  • Temperature-controlled with CO2-incubation
  • Nikon NIS Elements

Phone at microscope: xxxx

Contact: Barbara Biermann

Upright confocal laser scanning microscope (W1)

  • Laser lines: 458 nm, 476 nm, 488 nm, 514 nm, 543 nm, 633 nm
  • Filtersets: DD458/514, DD488/543, TD488/543/633, RSP500
  • Detectors: 3 photomultipliers
  • Optional: temperature-controlled stage
  • Software: Leica LCS

Upright stand FLIM (frequency domain)

Lambert LIFA with multi-LED (485 nm, 540 nm, 635 nm)

Filtersets for Fluorescein (long pass), Rhodamin (long pass) and GFP (short pass)

Phone at microscope: 12706

Contact: Thorsten Seidel

Inverted confocal laser scanning microscope (W01)

  • Laser lines: 458 nm, 488 nm, 514 nm, 543nm, 633 nm
  • Filter: LP 475nm, LP 505nm, LP 530nm, LP 560nm, LP 650nm
  • Software: Zeiss ZEN 2008

Phone at microscope: 5615

Contact: Thorsten Seidel

Light Sheet Microscope

Light sheet microscope for live imaging and cleared samples (W0-220)

  • Laser lines: 405 nm, 488 nm, 515 nm, 561 nm, 642 nm
  • 2 Hamamatsu Orca Flash cameras, separated by beam splitter
  • 4 Octagons for various applications

Phone at microscope: 67437

Contact: Thorsten Seidel

Fluorescence Widefield Microscopes

Leica DM6B motorized upright fluorescence microscope  (W0-220)

  • Light source: coolLED pE300
  • Objectives: 5x/0.15, 10x/0.32 Ph, 20x/0.55, 40x/0.80, 100x/1.32 Oil
  • Filter sets: DAPI, GFP, Texas Red, Cy5
  • Cameras: Leica K5 and Leica K3C
  • Software: Leica LAS X with Thunder module

Phone at microscope: 67437

Contact: Thorsten Seidel

Mobile Inverted Fluorescence Microscope for Teaching (W01-230)

  • Objectives: 5x, 10x, 25x, 40x LD PH, 60x
  • Filter sets: DAPI, FITC, RHOD
  • Light source: HXP-lamp

Contact: Thorsten Seidel

Microscopes, Polarization

Polarization Microscopy allows for visualization of birefringent structures such as cell walls, starch, spindles.

Polarization microscope (W0-211)

  • Inverted stand: Nikon Eclipse TE2000-S
  • Contrast methods: transmitted light (polarisator & analysator)
  • Software: Octax Eyeware
  • Camera: Octax camera system
  • Applications: imaging of birefringerant structures (spindles, cell walls)

Phone at microscope: 67436

Contact: Thorsten Seidel

Micro-Manipulation Setup

Inverted Stand, fluorescence microscope (W01-250)

  • Filter sets: CFP, YFP and FRET (CFP-YFP)
  • Camera: Zeiss MRm
  • Software: Zeiss Axiovision
  • Equipped with Eppendorf micro-injector

Contact: Thorsten Seidel

Other Equipment

Cell Sorter (R1 D2-103)

  • Laser lines 405 nm, 488 nm, 638 nm
  • Nozzle sizes: 70 µm, 100 µm, 130 µm

Contact: Barbara Biermann

Cytometer (UHG W0-218)

Laser lines 405, 488, 638 nm and ten filters (525 BP/40, 550DC SP, 655 DC SP, 620 BP 30, 755 LP, 710 DC SP, 660 BP 20, 595 DC SP, 450 BP 40, 575 BP 30, 730 DC SP, 695 BP 30/675 BP 20, 725 BP20, 750 DC SP, 550 BP 40)

Contact: Thorsten Seidel

Multimode Plate Reader (R1 D2-104)

Multimode plate reader with fusion optics (monochromator and filter-based optics) for absorption, polarization, fluorescence modes. Incubation with temperature control and CO2/O2-controller. 2 injectors are available.

Microscopy unit with dry objectives (4x/0.13, 10x/0.30) and filter sets for DAPI, FITC, TRITC and Alexa Fluor 633.  Predefined imaging protocols for cell confluency, kinetics, transfection efficiency, nuclei counting, cell vitality.

Contact: Barbara Biermann

Portable Incubator for mammalian cells

Contact: Barbara Biermann

Available for users. Please contact Dr. Thorsten Seidel (UHG) or Dr. Barbara Biermann (R1-D2).

  • For live cell imaging, small mobile incubators and a temperature-controlled stage can be obtained on request.

External Instruments

Single-molecule localization microscopy (R2, 3. Etage)

  • Laser lines: 405 nm, 488 nm, 561 nm, 640 nm
  • Objective 100x/1.45
  • 2 simultaenous channels (dichroic mirror splitter, 640 nm)
  • Hamamatsu Orca Flash4.0 v.3
  • lateral resolution of 20 nm
  • suitable for single molecule localization microscopy, TIRF and single particle tracking


Prof. Dr. Sven Thoms

Biochemie und Molekulare Medizin
Medizinische Fakultät OWL
Phone: 68502

Die Anschaffung des Mikroskops war möglich durch eine Sachspende der Marlies und Herbert Repkow Stiftung.

Omicron STM/AFM

operated in dynamic mode under ultrahigh vacuum conditions

Bruker AFMs (modified)

for atomic-resolution imaging at the solid-liquid interface

solvation layer mapping is possible with home-built hard- and software


Prof. Dr. Angelika Kühnle

Physikalische Chemie I
Fakultät für Chemie
Phone: 2045

Referenzen:
https://pubs.acs.org/doi/10.1021/acs.jpcc.1c06213
https://doi.org/10.3762/bjnano.11.74
https://doi.org/10.1103/PhysRevB.100.205410
https://doi.org/10.1021/acs.langmuir.6b03814
https://doi.org/10.1063/1.4952954

Dr. André Beyer

Physik supramolekularer Systeme und Oberflächen
Fakultät für Physik
Phone: 5364

Field of research / key experience: Development of computational approaches to harvest bioimage data.

Keywords: Bioimage Informatics, Computer Vision, Machine Learning, Remote Sensing, Medical Image Analysis, Information Visualization

Available resource: Online image annotation platform BIIGLE (www.biigle.de) for manual and AI-assisted image / video annotation (development since 2009, > 4,000 users).

 

Prof. Tim W. Nattkemper (tim@biigle.de)
www.uni-bielefeld.de/fakultaeten/technische-fakultaet/arbeitsgruppen/biodata-mining

Faculty of Technology
 

References

BIIGLE 2.0 - Browsing and Annotating Large Marine Image Collections. Langenkämper D, Zurowietz M, Schoening T, Nattkemper TW. Frontiers in Marine Science, 4,  2017, 83, DOI=10.3389/fmars.2017.00083, ISSN=2296-7745

Current trends and future directions of large scale image and video annotation: Observations from four years of BIIGLE 2.0. M Zurowietz, TW Nattkemper, FRONTIERS IN MARINE SCIENCE (section Ocean Observation), 2021, Manuscript ID: 760036A, https://doi.org/10.3389/fmars.2021.760036

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