This service includes tissue preparation, sectioning, immunolabeling with various dilutions of the primary antibody, coverslipping and labeling the slides. As a result, you will receive up to 30 immunostained tissue sections ready for microscopic observations. In addition, the experimental procedure used for the antibody titration will be provided.
Procedure: Following cryoprotection, tissue will be rapidly frozen in isopentane pre-cooled to -70°C. The frozen tissue will then be cut on a cryostat and mounted on gelatin-coated microscope slides (cf. Products, Cat. #PO101). Subsequently, sections will be processed on slides for immunostaining with the specific antibody at various dilutions according to the indirect immunofluorescence method¹. (for photo samples, cf. SI202).
- A quotation is required before placing an order.
- The investigator needs to provide both tissue and the specific antibody.
- Coons, A.H. (1958) Fluorescent antibody methods. In J.F. Danielli (ed): General Cytochemical Methods. New York: Academic Press, pp. 399-422.