| PRECOS
carries out a complete range of histochemical research and development
that can be offered as a stand-alone activity or in support of a wider
programme.
In addition,
PRECOS can assist in the development of specialised histochemical techniques
tailored to meet specific requirements.
Quantitative
Computer Aided Image Analysis
To aid interpretation, custom image analysis programs have been designed
by PRECOS scientists on QWin image analysis software (Leica Microsystems,
UK) to minimise observer subjectivity and provide robust, quantifiable
data. This advanced technology can be applied in the areas of:
Angiogenesis
- The
Human Angiokit System (TCS Cellworks):
PRECOS offers expertise in short term compound testing and evaluation
using human umbilical vein endothelial cells (HUVEC). End-point analysis
is carried out on CD31-stained HUVEC.
- Microvessel
Density Counting: CD31 labelled endothelial cell sprouts and
vessels are used to quantify solid tumour xenograft angiogenesis.
Assessment
of Proliferation and Cell Death
- Proliferation:
Xenograft proliferation, evaluated by measuring incorporation of the
thymidine analogue bromodeoxyuridine (BrdU) into cell DNA during S-phase
is a rapid and effective method for creating a ‘snapshot’
of proliferation.
- Apoptosis:
End-point apoptosis can be assessed in fresh, snap-frozen or fixed tissue,
fresh fixed cells or in archival systems by fragment end labelling.
- Necrosis:
Evaluation of necrotic cell death in haematoxylin and eosin counterstained
paraffin sections. Sections may be taken at multiple depths through
the test tissue to improve data analysis.
Histology
- Microscopic
Detection of Tumour Burden:
By haematoxylin and eosin counterstaining.
- Custom
Paraffin Tissue Microarrays: For rapid, comprehensive comparative
immunohistochemical analysis in up to 400 tissue samples on a standard
sized paraffin specimen block.
- Custom
Staining and Microscopy: PRECOS offers a full immunohistochemistry
service for all commercially available antibodies and further characterisation
of key proteins identified using high sensitivity Western blotting techniques.
|