ÌìÃÀ´«Ã½app

ÌìÃÀ´«Ã½app research and innovation

Imaging Facility

The University of ÌìÃÀ´«Ã½app Imaging Facility offers high-end instrumentation across microscopy, flow cytometry, and mass photometry. Our team of technical experts specialises in advanced support for cell and particle analysis across a broad range of biological and environmental applications.

Equipment and services

With 11 high-end Microscopes, 6 multi-parameter Flow Cytometers (including one Cell Sorter) and Mass Photometry our facility enables research throughout the University of ÌìÃÀ´«Ã½app and broader Illawarra region.

The facility is managed by two specialist staff who are available for instrument training, experimental development, application and technical support.

With 11 high-end Microscopes, 6 multi-parameter Flow Cytometers (including one Cell Sorter) and Mass Photometry our facility enables research throughout the University of ÌìÃÀ´«Ã½app and broader Illawarra region.

Bookings

If you are a new user please go to our  and register your details in the “I am a new user” section. If you are a registered customer please logon to the  with log in credentials.

Internal use fees

Facility

Hourly rate

Honours student subscription

Individual Cap*

Flow Cytometry (low end)

$25

$900

$1600 (hourly rate charged until 60 hours is reached, no further charge until 200 hours, $10/hour after that).

Flow Cytometry (all systems including high end) 

$45

$900

$2700 (hourly rate charged until 60 hours is reached, no further charge until 200 hours, $10/hour after that).

Light Microscopy user (low end)

$25

$900

$1600 (hourly rate charged until 60 hours is reached, no further charge until 200 hours, $10/hour after that).

Light Microscopy user (all systems including high end) 

$45

$900

$2700 (hourly rate charged until 60 hours is reached, no further charge until 200 hours, $10/hour after that).

IVIS Spectrum CT and REFEYN

$25

$900

 

$1600 (hourly rate charged until 60 hours is reached, no further charge until 200 hours, $10/hour after that.

Cell Sorting

$110/hour assisted FFS

(includes nozzle $40)

N.A

N.A

Fee for service (FFS) – staff assisted services

$100/hour

includes acquisition and basic analysis

N.A

N.A

**Individual user cap includes up to 200 hours of instrument use per facility. Hours may be accumulated across all instruments within the facility covered under the individual’s subscription. Usage ≥200 hours will be charged an hourly rate ($10/hour).

Commercial use fees

Facility

Commercial Subscription (Tier 1*)

Commercial Hourly Rate

Flow Cytometry (low end)

$6,000

$60

Flow Cytometry (all systems including high end) 

$12,000

$120

Light Microscopy user (low end)

$6,000

$60

Light Microscopy user (all systems including high end) 

$12,000

$120

IVIS Spectrum CT

$6,000

$60

Mass Photometry

$6,000

$60

Cell sorting

N.A

$300/hour assisted service, price includes setup and nozzle ($40)

Training on all systems

N.A

$500 per user, per Modality*

Fee for service (FFS) – on request

N.A

Contact Facility Manager

*Modalities are defined as Fluorescence Imaging, Flow Cytometry, Animal Imaging and Mass Photometry

Conditions for Use of the ÌìÃÀ´«Ã½app Imaging Facility (Microscopy, Flow Cytometry and Mass Photometry):

  1. All publications that in part of or in full arise from the use of the facility will need to include the following text in the acknowledgments section:
    We wish to thank and acknowledge the use of the University of ÌìÃÀ´«Ã½app Imaging Facility at Molecular Horizons under the management of Mr. Chris Brownlee, Any queries please contact Chris Brownlee for Flow Cytometry, or Nadia Suarez-Bosche for Advanced Light Microscopy. and Directorship of Professor Martina Sanderson-Smith.
  2. A faculty oversight committee has been formed to periodically review the operations of the facility as well as to approve any extraordinary exceptions to the following rules. The facility manager has the authority to approve daily operational exceptions as needed.
  3. The Imaging Facility is available to ÌìÃÀ´«Ã½app faculty, staff and students and also to members of Australian Academic Institutions at established campus approved recharge rates.
  4. The Facility does not have the resources for sample preparation except for live/dead staining of samples. Users are expected to determine what preparation techniques are needed for their own specimens and to perform them in their own lab.
  5. The Facility is open from 9 a.m. to 5 p.m., Monday through Friday. Experienced users may use the Facility after hours at the discretion of the Facility Manager and after proper training has been received.
  6. No user will be allowed to operate the microscopes, flow cytometry, mass photometry and ancillary equipment without proper training. The Facility Manager will determine if a potential user’s previous training is adequate, and if not, will provide such training. The ancillary equipment includes, but is not limited to, the:
  7. Hardware inc. pipettes and lab items
  8. Humidifiers and Temp controllers
  9. CO2 and Temp Controllers
  10. Users are expected to leave the microscopes, the scope rooms, and the wet lab in a condition such that the Facility is ready for the next user. These include but are not limited to:
  11. Properly shutting down the instruments
  12. Straightening up the rooms that were used
  13. Notifying the Facility Manager if there is a problem with the microscopes , flow cytometers, mass photometer or any other piece of equipment and writing down the occurrence in the associated logbook or via email
  14. Notifying the Facility Manager if the C02 or temperature controllers are not working
  15. Replenishing the sheath fluid and emptying the waste on the flow cytometry equipment
  16. Turning off all lights, including the hallway, and locking all doors when finishing work after hours
  17. No image files should be stored on the microscope computers and no external, file-storage devices (i.e. flash drives, CDs) should be attached to them. Digital files may be transferred to interim storage resources. Users are requested to remove their data from the FAF facility storage servers as soon as possible. Data older than two months will be deleted by the Facility Manager without owner notification.
  18. All established safety procedures need to be followed and all hazardous waste is to be properly disposed.
  19. No user should attempt to fix any equipment problems, regardless of how small or insignificant they may appear to be. The Facility Manager’s contact information is posted outside of each equipment room and a 24 hour phone number is listed.
  20. There will be no restrictions on how much time a user can schedule outside of the normal work week but courtesy to other users is expected.
  21. A user will be charged for a scheduled appointment if the user does not show up or delete the appointment from the scheduler. Charging for the session will begin at the scheduled time.
  22. Users who receive microscope, flow cytometry and/or ancillary equipment training will be charged both for the microscope time. The Facility Manager’s and Senior Tech staff’s time is currently uncharged.

Microscopy

To select the microscope best suited to your application please refer to the .

Common applications:

  • Routine Bright field microscopy examination
  • Designed for cell and tissue culture work

Features:

  • Camera stand outfit (MC170). Capture resolution of 5 Mpixels and up to 30 fps
  • 4 position slider for S40 condenser (bright field and phase contrast imaging)
  • 4 Objectives (N Plan 5X, Hi Plan10, 20X, 40X)
  • Object Guide
  • Universal holding frame M

Software:

  • Leica Application Suite (LAS)

Common applications:

  • Sample preparation
  • Carry out close work such as dissection, microsurgery
  • Viewing insects, crystals, plant life, circuit boards etc.

Features:

  • Zoom ratio: 6:1
  • Magnification range: 6.3x - 40x (1x objective, 10x eyepieces)
  • Resolution up to 225 lp/mm (1x objective, 10x eyepieces)
  • Transmitted light base TL5000, bightfield and two sided darkfield
  • Coarse Focus drive, column 300mm
  • Objective achromat 1.0x, WD 90mm

Common applications:

  • PAULA is a smart digital imager designed for cell culture lab
  • Transfection efficiency, cell counting, confluence check and wound healing work

Features:

  • Alignment free Phase contrast, red and green (emission) fluo LEDs
  • Magnification: 10x with a 4x digital zoom
  • Illumination: LED
  • An integrated barcode reader can scan and identify culture flasks quickly and reliably

Software:

  • PAULA Software includes image and t-lapse acquisition, data and user management
  • Controlled with a touch monitor and a NUC PC (iOS, Android and Windows)

Common applications:

  • Ideal for fluorescence and brightfield laboratory cell analysis
  • Image 2D cell cultures (monolayer Adherent best)
  • Tissue sections

Features:

  • DM IL includes LED Illumination for transmitted light
  • CoolLED with Filter sets: DAPI /FITC / TXR (mCherry)/ Y5
  • Phase Contrast and Fluorescence NPLAN objectives: 5x/0.12 PH, 10x/0.25 PH, 20x/0.35 PH, 40X/0.55 PH
  • Condenser S 40 / 0.45
  • Object guide
  • Universal holding frame M
  • Trinocular tube HC ILT, with viewing angle 45° beamsplitter 0/100%, 100/0%
  • Leica DFC3000 G digital high-sensitivity monochrome camera. CCD technology 1.3 MPixel with a pixel size of 3.75 μm.

Software:

  • Leica Application Suite X (LAS X)

Common applications:

  • Imaging of organism used for developmental or molecular biology research, such as Drosophila, C. elegans, zebrafish, etc.
  • 3D tissue imaging
  • Suited for demanding high-speed fluorescence applications
  • THUNDER Imager delivers blur-free images revealing the fine structural details of live organisms, while keeping them under optimal physiological conditions.

Features:

  • Leica M205 FA optics carrier fully motorized with: magnification, three position fluorescence filter turrent, fluorescence light shutter, and Iris diaphragm
  • Zoom-magnification changer 20.5:1
  • Magnification area: 7.8x-160x
  • Resolution up to 525 lp/mm (1x objective, 10x eyepieces), maximum resolution up to 1050 lp/mm (2x objective, 10x eyepieces).
  • Motor focus drive short 420mm
  • Triple Beam TM: Separate optical beam path for fluorescence illumination
  • SmartTouch TM control unit
  • White LED light source for fluorescence (Lumencor SOLA-SMII (365nm Version).
  • Wavelength range: 350 – 680 nm CFP/GFP/mCherry
  • Motorized XY-Scanning stage (Leica LMT260)
  • Leica DFC9000 GTC camera:
    • Is a deep-cooled 4.2 MP sCMOS camera with a maximum of 82% quantum efficiency
    • ~90 frames per second acquisition speed, and extreme low dark current of 0.14e-/p/sec.
    • Pixel: 2048 x 2048 (4.2 Megapixel). Pixel size: 6.5 μm

Software:

  • Leica Application Suite X (LAS X)
  • LAS X Navigator
  • THUNDER Imager offers three exclusive computational clearing modes:
    • Instant Computational Clearing (ICC) for instantaneous removal of out of focus background
    • Small Volume Computational Clearing (SVCC) dedicated to thin specimen
    • Large Volume Computational Clearing (LVCC) dedicated to thick specimen

Common applications:

  • THUNDER Imager is designed for imaging of cell culture assays
  • Imaging of 3D cell cultures and tissue, cell migration, tumors, spheroids, neurospheres, organoids, etc.
  • Maintains optimal physiological conditions by minimizing photobleaching
  • Provides high-performance imaging and high-throughput of data with a better workflow efficiency and statistics

Features:

  • Leica DMi8 fully motorized, inverted research stand
  • Hardware based adaptive focus control (AFC) for drift correction and fast focusing in multi well applications
  • Closed loop focusing system for high precision focusing with reproducibility of 20 nm
  • Nosepiece, motorized 6-fold revolver
  • ICT condenser prism
  • Universal holding frame KM, Click-In
  • Touch screen
  • Leica DFC9000 GTC camera: 4.2 MP sCMOS camera with ~90 frames per second acquisition speed, and pixel size of 6.5 μm
  • Incubator i8 - BLACK LS.
  • Temperature controller, heating unit and CO2 controller

Light Sources and Filters:

  • LED Source
  • External Filter Wheel (EFW) slider for high speed acquisition – Filter set - quad cube for imaging (DAPI/405, FITC, TRITC, Cy5)
  • 4 filter sets with Excitation wavelengths: 391/32, 479/33, 554/24, 638/31. Emission wavelengths: 435/30, 519/25, 594/32, 695/58. Dichroics: 415, 500, 572, 660
  • -Includes filter wheel for EFW (5 positions with emission filters: 440/40, 510/40, 590/50, 700/75, 100% transmission)

Objectives:

  • HC PL FLUOTAR 1.6x/0.05
  • HC PL FL L 20x/0.40 CORR PH1
  • HC PL APO 20x/0.80 PH2
  • HC PL APO 40x/0.95 CORR
  • HCX PL APO 40x/1.10 W CORR
  • HC PL APO 63x/1.40-0.60 OIL

Software

  • Leica Application Suite X (LAS X)
  • LAS X Navigator
  • LAS X 3D Analysis and Visualization
  • THUNDER Imager offers three computational clearing modes:
    • Instant Computational Clearing (ICC) for instantaneous removal of out of focus background
    • Small Volume Computational Clearing (SVCC) dedicated to thin specimen
    • Large Volume Computational Clearing (LVCC) dedicated to thick specimen

Overview:

Total Internal Reflection Fluorescence (TIRF) is a microscopy technique for the visualization of fluorophores that are immediately adjacent (<250 nm) to a glass coverslip. TIRF microscopes direct the excitation laser at an oblique angle to create total internal reflection that generates a highly restricted electromagnetic field (or evanescent waver) within the specimen.

Common applications:

  • To study molecular events at or near the cell surface such as cell adhesion, neurotransmitters secretion, binding of cells by hormones
  • Can be used for single molecule localization research
  • Tracking movement in the cell membrane, endocytosis, exocytosis, etc.

Features:

  • Eyepieces HC Plan S 10x/25 Br. M
  • Motorized coarse and fine focus in combination with Leica adaptive focus control (AFC)
  • Scanning Stage Leica with 1mm spindle
  • Universal holding frame KM, Click-In and Universal mounting frame K100
  • Brightfield / Phase Contrast / Darkfield / DIC motorized
  • Motorized Objective Prism Turret
  • Motorized Condenser with fixed head S28 / N.A. 0.55
  • Analysator Cube for motorized DIC
  • ICT-condenser prism
  • -TIRF Infinity Scanner
  • Leica DFC9000 GTC camera: 4.2 MP sCMOS camera with ~90 frames per second acquisition speed, and pixel size of 6.5 μm
  • Incubator i8 BLACK LS with laser safety
  • Temperature controller, heating unit and CO2 controller

Light Sources and Filters:

  • LED with TTL-Shutter
  • External light source EL6000 with light guide
  • Laser module 488nm (150mW) and 638nm (150mW)
  • Motorized 6 -fold Filter Turret:
    • Filter cubes LED 405, GFP, TXR, and LED 620
    • Filter cube QWF-T. Excitation 400/28, 490/20, 561/15, 640/20, Dichroic: 422, 508, 576, 658.
      Emission: 448/48, 531/32, 598/40, 705/90

Objectives:

  • HC FL PLAN 5x/0.12
  • HC PL FLUOTAR 10x/0.32 PH1
  • HC PL APO 20x/0.80 PH2
  • HC PL APO 40x/0.85 CORR CS
  • HC PL APO 63x/1.40-0.60 OIL
  • HC PL APO 100x/1.47 OIL CORR TIRF

Software:

  • Leica Application Suite X (LAS X)
  • LAS X Navigator

Overview:

Confocal laser scanning microscopy is one of the most popular techniques for imaging fluorophores in biological specimens.  This optical imaging method increases optical resolution, contrast and in-focused images by removing out of focus light during image collection.  This is achieved by using a spatial pinhole. Confocal specimens are illuminated by a focused point of laser light that is scanned across the specimen in the horizontal plane.  Capturing multiple 2D images at different depths enables the reconstruction of 3D structures within a sample.

Common applications:

  • Powerful microscope (workhorse) suited to high quality imaging of fixed and live cells through time
  • Ideal for 3-D imaging, time course experiments, real time visualisation of rapid cell responses
  • Delivers high resolution required for multi-dimensional observation of cell and tissue morphology as well as precise molecular localisation

Features:

  • Leica TCS SP8 confocal scanning microscope
  • Closed Loop Focus with Adaptive Focus Control (AFC)
  • Spill protection for DMi8
  • Optical Outfit + motorized ICT
  • Scanning stage inverted
  • Universal holding frame K
  • Condenser prisms for transmitted light interference contrast
  • Tandem scanner 12 kHz
  • Switchable resonant and non-resonant (1 -1800 Hz) mode for optimal scanning speeds
  • Ludin Environmental Chamber (gas and temperature controller)
  • Camera sCMOS Hamamatsu W-View Gemini provides excellent transmittance across a broad range of wavelength (40nm to 800nm). Simmultaneous image acquision of dual wavelength images. Resolution of up to ~2000 pixels x 1000 pixels per image

Light Sources and Filters:

  • External light source EL6000
  • Laser 405 nm DMOD Compact, Laser blue 488 nm, Green 552 nm, Red 638 nm
  • Two internal detector channels (PMT), one internal detector channel HyD (SP GaAsP-Detector)
  • Transmitted Light Brightfield Detector
  • Filter cube DA/FI/TX

Objectives:

  • HC PL FLUOTAR 20x/0.55
  • HC PL APO 40x/1.30 OIL CS2
  • HC PL APO 63x/1.40 OIL CS2
  • HC PL APO 93x/1.30 GLYC motC STED W

Software and modules available:

  • Leica Application Suite X (LAS X)
  • LAS X Navigator
  • LAS X 3D Visualisation
  • Huygens Base package for confocal (De-convolution)

Overview:

SP8 FALCON (FAst Lifetime CONtrast) a powerful microscope equipped with a truly integrated solution for Fluorescence Lifetime Imaging (FLIM), Fluorescence Resonance Energy Transfer (FRET) and Fluorescence Correlation Spectroscopy (FCS) to investigate cellular physiology and explore dynamics in living cells.

  • The FLIM approach on SP8 FALCON is based on a confocal scan head with field-programmable gate array (FPGA) electronics, pulsed laser excitation and fast, spectral single-photon counting detectors
  • Fluorescence Resonance Energy Transfer (FRET) is an optical technique used to detect molecular interactions and requires specific donor and acceptor fluorophore pairs. Measurements of FRET efficiency can be used to determine if two fluorophore are within a certain distance of each other
  • Fluorescence Correlation Spectroscopy (FCS) is a technique that allows the measurement of diffusion coefficients and concentrations for fluorescing constructs

Common applications:

  • The applications of FLIM are many: from ion imaging and oxygen imaging to studying cell function and cell disease.
  • FRET is a useful tool for quantifying protein-protein interactions, protein–DNA interactions, protein conformational changes, and to detect the location and interactions of genes and cellular structures including intergrins and membrane proteins
  • FCS and FLCS can measure any fluorescently labelled molecules in solution (usually water or buffer solution), on membrane and even inside living cells

Features:

  • Leica TCS SP8 Flexible Supply Unit White Light Laser, DMi8 CS Bino
  • Closed Loop Focus with Adaptive Focus Control (AFC)
  • Turret cooling for DMi8
  • Spill protection for DMi8
  • Optical Outfit + motorized ICT
  • Scanning stage inverted
  • Super Z Galvo stage type H
  • Ludin Environmental Chamber (gas and temperature controller)
  • Tandem scanner 8 kHz
  • Leica DFC7000 T Camera: The state-of-the-art CCD sensor provides quality and speed to reproduce colors faithfully with intelligent interpolation to match illumination settings
  • Features 2.8 megapixel with a pixel size resolution of 4.54 µm, 40 fps at full resolution and 50 fps with exclusive turbo mode

Light Sources and Filters:

  • External light source EL6000
  • Laser 405 nm AOTF Flexible
  • White light laser (WLL) for Acousto-Optical Beam Splitter (AOBS) system. Excitation lines from 470 to 670 nm.
  • Pulse frequency max. 80 MHz, variable by means of pulse picker
  • Filter cube DA/FI/TX and filter cube Y5
  • Transmitted Light Brightfield Detector
  • Four Internal Detector Channels:
    • Internal Detector Channel HyD SMD 1
    • Internal Detector Channel PMT 2
    • Internal Detector Channel PMT 3
    • Internal Detector Channel HyD SMD 4

Objectives:

  • HC PL APO 10x/0.40 CS2
  • HC PL APO 20x/0.75 IMM CORR CS2
  • HC PL APO 40x/1.10 W CORR CS2
  • HC PL APO 63x/1.40 OIL CS2
  • HC PL APO 86x/1.20 W motCORR STED W

Software:

  • Leica Application Suite X (LAS X)
  • LAS X Navigator
  • LAS X 3D Visualisation
  • FALCON Fluorescence Life-time Imaging Microscopy (FLIM) with WLL
  • LAS X Phasor FLIM
  • FALCON enables Fluorescence Lifetime Correlation Spectroscopy (FLCS) experiments
  • LAS X includes FLIM-FRET analyzer
  • Confocal Super-Resolution LAS X LIGHTNING Expert

Applications:

The Reversible Saturable Optical Fluorescence Transitions (RESOLFT) superresolution microscopy.

RESOLFT stands for a general switching principle: the switching mechanism does no longer need to be purely electronically but can include switching mechanisms like for example conformational changes of a molecule. Strictly speaking, the STED method is one possible implementation of the RESOLFT concept. The approach is similar as shown for STED – a beam scanning setup with overlapping beams of the excitation and the switching beam.

Features:

  • Superresolution RESOLFT channel compatible with fast switching GFP variants
  • -Two fast scanning simultaneously recording confocal channels
  • GFP, 488-dye optimized
  • Motorized pinhole
  • State-of-the-art fluorescence widefield and confocal stand (IX83)
  • Proprietary, very-compact linear Quad-Scanner
  • Software solution including data analysis package

Common applications:

High precision, compact micromanipulator system to simplify intracellular injection. It is capable of delivering precise nanoliter volumes of diverse compounds and biomolecules.

Features:

  • Inverted microscope Eclipse Ti2-U main body
  • DIC Polarizer
  • Combined 3D motor-drive coarse manipulator and 3D oil-hydraulic fine manipulator
  • Pneumatic Microinjector (IM-11-2)
  • Electric Microinjector 240V (IM-400)
  • Suction Unit for IM400 (IM-400B)

Objectives:

  • CFI Plan Fluor 4x/0.13, W.D. = 17.1 mm
  • CFI Plan Fluor 10x/0.30, W.D. = 16.0 mm
  • CFI Super Plan Fluor ELWD 20x/0.45, W.D. = 8.2-6.9 mm
  • CFI Super Plan Fluor ELWD 40x/0.6, W.D. = 3.6-2.8 mm

Flow Cytometry

To select the flow cytometer best suited to your application please refer to the .

Common applications:

  • Quantifiable cellular analysis of single cells
  • High speed analysis of cells from sources such as human, mouse or cell culture

Features:

  • Easy to use
  • Excellent signal to noise ratio
  • High speed (up to 5,000 cells per second)
  • Primarily tube-based acquisition - HTS (High Throughput Screening) option available
  • Analysis of sample up to 16 Fluorescent Parameters plus Forward and Side Scatter
  • Multi-colour acquisition
  • Simple Compensation matrix setup via DiVa Wizard
  • Individual laser on/off capabilities
  • Great for a wide range of applications 

Software:

  • BDFACSDiva™ Software

Configurations: 

Common applications:

  • Quantifiable cellular analysis of single cells
  • High speed analysis of cells from sources such as human, mouse or cell culture
  • 96 well plate loader for high through put screening automatically installed

Features:

  • Easy to use
  • Excellent signal to noise ratio
  • High speed (10x other flow cytometers 1ml / minute acquisition using Acoustic focusing technology
  • 96 well plate analysis with anti-clog technology
  • Analysis of sample up to 11 Fluorescent Parameters plus Forward and Side Scatter
  • Multi-colour acquisition
  • Simple Compensation matrix setup via Attune NxT Software
  • Great for a wide range of applications 

Software:

  • Attune NxT™Software (analysis station available offline)

Configurations: 

Common applications: 

  • Quantifiable cellular analysis of single cells

Features:

  • Very easy to use
  • Tube based analysis
  • Analysis of sample up to 5 Fluorescent Parameters plus Forward and Side Scatter
  • Multi-colour acquisition
  • Great for simple applications
  • Compact 

Software:

  • BDAccuri™ C6 Plus Software

Configurations: 

The MA900 from Sony meets the needs of most sorting applications, supporting 12 fluorescence parameters and 4-way sorting.

Powerful, modern technologies built into the MA900 system include a patented micro fluidic chip-based design, comprehensive fluidic controls, and advanced automation that dramatically simplifies operation to make sorting less subjective and improve reliability.

The MA900 offers choice and flexibility, enabling the detection of up to 14 parameters. Currently equipped with 2 excitation lasers: 488 nm and 638 nm. Free-form PMTs enable detection of fluorescence signals from each beam spot, allowing detection of up to 12 fluorescence parameters and two scatter parameters.

Configurations: 

Mass photometry

Mass photometry is a revolutionary new way to analyze molecules. It enables the accurate mass measurement of single molecules in solution, in their native state and without the need for labels. This approach opens up new possibilities for bioanalytics and research into the functions of biomolecules

Animal imaging

The IVIS® SpectrumCT preclinical in vivo imaging system expands upon the versatility of the IVIS Spectrum by offering 2D and 3D imaging capabilities but includes integrated low-dose microCT ideal for longitudinal studies. The system provides researchers with greater insights into complex biological systems by enabling simultaneous molecular and anatomical non-invasive imaging in animal models.

Our team

Mr Chris Brownlee
Senior Technical Officer, Imaging Facility
Flow Cytometry 

Phone: +612 42218060
Mobile: +61 04332 29271
Email: chris_brownlee@uow.edu.au

Dr Nadia Suarez-Bosche
Senior Technical Officer, Imaging Facility
Advanced Light Microscopy

Email: nadia_suarez-bosche@uow.edu.au 

Dr Claire Stevens
Histology and Microscopy Specialist 

Email: claire_stevens@uow.edu.au  

Contact us


Contact the ÌìÃÀ´«Ã½app Research Infrastructure team to connect with the right facilities and experts and achieve your goals.