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  • Faculty of Biology, Medicine and Health
  • Research
  • Technology platforms
  • Histology
  • Faculty of Biology, Medicine and Health
  • Research
  • Technology platforms
    • Bioimaging
    • Bioinformatics and computation
    • Biological services
    • Biomolecular analysis
    • Clinical and preclinical imaging
    • Electron microscopy
    • Flow cytometry
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    • Histology
    • Mass spectrometry

Histology

From tissue to image – processing, sectioning, staining and labelling

The Histology Core Facility is more than a service. We are an integral part of your tissue imaging project and can guide you every step of the way.

We work closely with the Bioimaging Core Facility to ensure that your sample is appropriately processed for downstream imaging applications.

Traditional techniques such as paraffin embedding and histological staining are complemented with newer techniques such as cryo-sectioning and automated antibody labelling.

We reduce the need for thin sectioning with the use of tissue vibrotomes and whole tissue clearing.

In addition to The University of Manchester’s researchers, we also support external access.

On this page:

  • How we work
  • Applications
  • Technologies and equipment
  • Publications and outputs
  • External access
  • Contact us
  • Other technology platforms

How we work

More than cutting thin tissue sections

Histology is about getting your sample prepared in the best way for imaging.

Working closely with the Bioimaging Core Facility we understand what is needed to produce high-quality, quantitative images on tissue sections and whole tissues.

We offer two ways of creating excellent tissue sections:

User training

We provide full user training on the microtomes and cryostats.

Close up of a cryostat.

Full service solutions

Our experienced histology technicians will process and section samples as a service to groups that do not have the time or the training.

Slide overview of results obtained from the fully automatic digital slide scanner.

Drop-off services

We also offer a range of drop-off services such as tissue processing, automated histological staining and automated antibody labelling.

Haematoxylin (blue) and Eosin (pink) (H&E) staining on mouse kidney section.

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Applications

Access the latest histological techniques

We are constantly investing in the facility to ensure that our users have access to the latest developments in histological techniques.

Advancements in tissue sectioning techniques, labelling technology and optical imaging, mean that we offer many of these new techniques alongside traditional paraffin and resin thin sectioning.

Small tissue samples

Paraffin embedding and sectioning of small tissue samples.

H&E staining on mouse skin 'rolled up' and cross sectioned.

Cryo-sectioning

Cryo-sectioning of fixed frozen tissue samples.

Haematoxylin (blue) and Eosin (pink) (H&E) staining on mouse liver section.

Vibratome thick sectioning

Vibratome thick sectioning of fresh tissue samples.

Histological section of an elastic artery (human aorta). Orcein staining.

Automated histological staining

Automated histological staining such as H&E, Masson’s Trichrome and Picrosirius Red.

Histological section of the ovary stained with Masson's trichrome.

Automated IHC labelling

Automated IHC labelling for a range of cell markers using validated kits.

Immunofluorescence image of cancer cells.

Whole tissue clearing

Whole tissue clearing to remove the need to section the tissue at all.

A technician prepares histology sections.

Multiplex imaging

Multiplex imaging through multiple rounds of antibody labelling, imaging and antibody stripping provides the ability to localise multiple protein markers within the tissue section. This multiplex spatial imaging provides a link between histology, bioimaging and the spatial transcriptomics available in the Genomic technology facility and Hyperion imaging system in the Flow cytometry facility.

Single human cell stained with multiple antibodies.

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Technologies and equipment

Benefitting from investment

Investing in our equipment ensures that the Histology Core Facility remains at the cutting edge.

We are constantly investing in new equipment and technology to ensure that we can offer our users access to the latest and most appropriate techniques.

The tissue processors are run as a drop-off service and have a range of pre-programmed runs available. However, we are always flexible and can set up a new programme to meet your needs.

Cassettes are then transferred to the embedding centres ready for the user to paraffin embed the tissue samples in the desired orientation.

  • 2 x Leica ASP300S automated tissue processors
  • 3 x Leica HistoCore Arcadia embedding centre and coldplates

Traditional paraffin block thin sectioning is still one of the main techniques used by histologists.

We have a range of microtomes available within the facility and provide full and ongoing training to the user.

We are able to offer microtome sectioning as a service. Contact us for more information.

  • Leica RM2235
  • 2 x Leica RM2255
  • Leica Histocore Multicut

Cryosectioning overcomes many of the limitations of paraffin embedded tissue such as the need for antigen retrieval before IHC and the reduction of antibody sensitivity.

The technique itself is quite straightforward to understand but requires skilled training and experience to fully realise its potential.

We are able to offer cryosectioning as a service. Contact us for more information. 

  • 2 x Leica CM3050S
  • 3 x Leica CM1950

We run the auto-stainer as a drop-off service and have a range of stains preloaded into the machine.

We are happy to configure new programmes or modify the timings of the existing ones to meet your requirements.

Stains offered include: H&E, Masson’s Trichrome, Picrosirius Red, FastRed/FastBlue, and Verhoeff-Van Giesons.

The automated staining system is connected to an automatic coverslipper providing a convenient solution for staining and mounting large numbers of slides ready for imaging in the Bioimaging Core Facility’s digital slidescanner.

  • Leica ST5010
  • Leica CV5030

The Leica BOND RX provides a convenient and reliable way of performing IHC, FISH, multiplexing and other labelling reactions.

The system uses validated reagents to automatically label the individual slides. There are a wide selection of reagents available.

  • Leica BOND RX
  • View a selection of validated Novacast antibodies

Optical techniques such as confocal microscopy do not require very thin tissue sections such as those from a microtome or cryostat.

It is possible to cut fresh tissue on a vibratome and then fixed and label with fluorescent markers. The sectioning is then done optically on the confocal, providing excellent spacial information for techniques such as neurone tracking or vasculature mapping. 

  • 2 x Leica VT100S

Imaging depth in fluorescently labelled tissue is limited by the opacity of the tissue. The high lipid content of tissue restricts the amount of excitation light that can reach the fluorophore and reduces the amount of emitted light that can get back out of the tissue.

By using clearing techniques to remove the lipid it is possible to produce an optically transparent tissue which allows imaging millimetres deep into the sample.

This technique is excellent for understanding the three-dimensional nature of complex tissues such as the brain, lung and even whole organisms.

There are numerous clearing techniques and we provide access to a simple-to-use automated X-CLARITY clearing system.

  • X-CLARITY

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Publications and outputs

Supporting high impact publications

High impact publications often rely on access to state-of-the art imaging systems. The Histology Core Facility provides those systems.

We are an essential resource that contributes to numerous high impact publications every year.

Here are some of the recent highlights.

Oncogene, 2021.

We show that high levels of ERK5 is a predictive marker of metastatic breast cancer using a combination of classical histological stains and specific antibodies to differentiate between the cancerous, normal and control tissue.

  • DOI: 10.1038/s41388-021-01798-2

BMC Immunology, 2021.

This paper elucidated the role of β2 integrin in dendritic cell migration during infection with the nematode worm Trichuris muris. Paraffin wax sections were used for classical histological staining, while cryosectioning allowed preservation of tissue antigenicity to provide the ideal sample for immunofluorescent labelling with specific antibodies.

  • DOI: 10.1186/s12865-020-00394-5

Nature, Scientific Reports, 2021.

Glucocorticoids (GCs) are widely prescribed anti-inflammatory medicines, but their use can lead to metabolic side-effects increasing food intake and modifying peripheral metabolism. As part of this study, wax sectioning was used for classical histological staining to look at lipid changes in tissue, and cryosectioning to provide the ideal sample for immunofluorescent labelling with specific antibodies against the glucocorticoid receptor and hypothalamic AgRP neurones.

  • DOI: 10.1038/s41598-021-93378-3

Molecular Systems Biology, 2021.

Thick sections of fresh mouse trunk tissue were prepared on a vibratome before timelapse imaging on a confocal microscope. This provides 200um thick tissue, which is ideal for confocal imaging and ensured that the yellow fluorescent protein (YFP) in the tissue was unaffected due to the absence of any processing steps.  Cryosectioning was then used to provide thin tissue sections for immunofluorescence labelling experiments.

DOI: 10.15252/msb.20209902

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External access

Working with other academic institutions and industry

Although primarily focused on supporting research at The University of Manchester, we are also able to support work from other academic institutions and industry.

Academic institutions

We are happy to provide access to all our histology equipment to users from other institutions.

We are also happy to provide a full histology service from tissue processing through to sectioning and staining.

It is also possible to extend this service through to whole slide scanning through our links with the Bioimaging Core Facility.

Contact us for further details.

A researcher preparing slides with paraffin sections.

Industry

We have worked for a number of multinational companies, both on an individual basis and as part of packages of work involving multiple facilities.

Work may be on a collaborative basis or purely as a service provision.

All work is fully documented and contractual, and non-disclosure compliance is assured.

Please contact our Business Development Manager for further details if you are interested in accessing the facility:

Dr Joanne Flannelly
Email: joanne.flannelly@manchester.ac.uk

Scientist embedding tissues in paraffin blocks for sectioning.

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Contact us

Find out more

Get in touch for further information or to inquire about using our facility.

Dr Peter March, Senior Experimental Officer

Email: peter.march@manchester.ac.uk
Telephone: +44 (0)161 275 1571

The Michael Smith Building
The University of Manchester
Oxford Road
Manchester
M13 9PT

Maps and travel

We are based in the Michael Smith Building (Building 71 on the University campus map).

See: University maps and travel section

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Technology platforms

Technology platforms

We have a pioneering environment and facilities for research, innovation and technology development.

Technology platforms main page

Molecular

  • Biomolecular analysis
  • Electron microscopy
  • Genomic technologies
  • Mass spectrometry

Cellular

  • Bioimaging
  • Flow cytometry
  • Genome editing

Organismal

  • Biological services
  • Clinical and pre-clinical imaging
  • Fly Facility
  • Histology
  • Manchester Clinical Research Facility (MCRF)

Cross facility support

  • Bioinformatics and computation

Contact us

  • +44 (0) 161 306 6000
  • Contact details

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The University of Manchester
Oxford Rd
Manchester
M13 9PL
UK

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