UNIVERSITY OF WASHINGTON | SEATTLE, WASHINGTON
Cellular & Molecular Imaging Core
CMIC Services
- Tissue fixation and processing for light microscopy: Preparation of fixative solutions, performing vascular perfusions, collecting tissues, and freezing tissues.
- Embedding and sectioning: Paraffin embedding of fixed tissues and embedding in OTC compound for cryostat sectioning. Paraffin sectioning as well as cryostat sectioning of frozen tissues. Sections are mounted on slides for staining.
- Histological and histochemical staining: Routine methods such as hematoxylin and eosin, and specialized histochemical staining techniques such as thioflavin S and Congo red for islet Amyloid, Oil red O for adipocytes, ß-galactosidase for lacZ reporter gene expression, and TUNEL for apoptosis.
- Immunocytochemical staining: Peroxidase and fluorescent-labeled antibodies and related methods, including multiple labeling applications.
- In situ hybridization: mRNA localization using isotopic (film and emulsion autoradiography) and non-isotopic methods and with labeled riboprobes and oligonucleotides, including multiple ISH labeling.
- Flow cytometry: The core oversees the operation and maintenance of flow cytometry instruments for DERC investigators and trains users.
- Digital image acquisition: Images of cellular and histological preparations by various microscopic optical modalities including confocal microscopy.
- Technical assistance: Personnel to perform services and train users in protocols and use of analytical equipment for cellular and molecular imaging.
- Consultation: Consulting assistance with protocols and procedures, as well as with design of their studies and interpretation of results. Consultation is a major function of the core and involves collaborative interactions of affiliates with the core directors.
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