Tissue Microarray (TMA) Lab
The major goal of this facility is to provide TMA technology for UF investigators. All services are available from processing samples into donor blocks and evaluating regions of interest to TMA design, construction, sectioning, and staining. Any stain that can be used on a paraffin section can also be performed on a TMA. Fees for TMA construction are based on technical support time and supplies. Individuals can also be trained to construct arrays.
Please contact us before submitting the TMA Service Request form.

Using an HE stained slide of the donor block for guidance, the area(s) of interest is removed as a core from the donor block with the appropriate sized needle and transferred into the recipient block (up to 4 recipient blocks can be made at one time). The block is sealed with paraffin and stored at -20 until sectioned. Slides are sealed with paraffin to maximize stability.
TMA slides can be stained as for any paraffin slide.
Routine TMA Configurations
Needle size |
Spacing between samples |
Array Format |
Total # Cores |
0.6 mm |
0.2 mm |
20 x 20 |
400 |
1.0 mm |
0.3 mm |
16 x 13 |
208 |
1.5 mm |
0.4 mm |
11 x 9 |
99 |
Representative TMA
Mouse Lymphoid TMA (Spleen, Pancreatic lymph node, Thymus; 3 fixatives): H&E image; CD3 IHC
Human brain tumor TMA
(Dr. T. Yanchis): H&E images at increasing magnification
Services:
-
Consultations on TMA design and analysis
- Donor block preparation and staining
- TMA construction- training available if you want to make the TMA
- Need animal or human tissue donor blocks? Ask about our paraffin and frozen archives.
Equipment:
- Beecher Tissue Microarrayer (0.6, 1, 1.5 mm punches)
- Four recipient block holder
- Olympus dissection and viewing microscopes
- Aperio GS slide scanning
- Image processing and analysis
TMA Links:
Beecher Instruments Trouble Shooting Guide
Stanford TMA
UVA TMA
Johns Hopkins Pathology TMA Core : Principles, Uses and Construction of TMA
Yale Pathology TMA facility
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