Materials & Methods > Core B > Immunohistochemical Staining for cleaved caspase-3 (Apoptosis)
 

Turk Lab Standard Operating Procedure (SOP) for Immunohistochemical Staining for cleaved caspase-3 (Apoptosis)

Materials
Literature

1. Cut paraffin sections @ 4 microns and place on positively-charged slides (Surgipath X-tra Slides® 00210)

2. Microwave slides briefly 1-2 min. on high power until paraffin is just melted or bake in 60 degree C oven for 1 hour.

3. Deparaffinize , run slides to water and perform steamer (Black and Decker HS2000 vegetable steamer) retrieval @ 90-100 C in Dako Target Retrieval solution (S1699) for 30 min. with 20 min. room temperature (RT) cooling time. Distilled water rinse several times.

4. Quench endogenous peroxidase with fresh 3% H202 for 5 min.

5. Rinse with distilled water several times and place in Tris with Tween buffer (Dako S3306)

6. Block tissue with A/B block (Vector) for 15 min. each with a Tris withTween buffer rinse between and after.

7. Wipe around tissue and block with protein block (Dako X0909 ) for 10 min.

8. Drip protein block off slide and apply primary antibody for overnight incubation. Primary antibody = 1:50 dilution of rabbit anti-13 amino acid peptide from the carboxyl terminus of human and mouse caspase-3 p18 subunit (source: Trevigen Catalog Number 2305-PC-100) The antibody can be used on formalin-fixed paraffin-embedded tissue using positive control porcine corpus luteum (Figure 1).

9. Next day place slides in Tris with Tween buffer and rinse once.

10. Wipe around tissue and apply secondary antibody for 30 min. incubation at RT. (Dako, LSAB+ Kit, K0690)

11. Tris with Tween buffer rinse.

12. Apply label (Streptavadin, Dako , LSAB+ Kit K0690) for 30 min. at RT

13. Rinse with distilled water several times.

14. Wipe around slides and apply diaminobenzidine (DAB Dako, K3466) for 5-10 min., monitor slides and place in water when desired intensity has been reached.

15. Rinse several times with distilled water.

16. Apply DAB enhancer (Dako, S1961) for 5 min. at RT.

17. Rinse several times with distilled water.

18. Give a 1 min. hematoxylin counterstain followed by 10 seconds in 1% acid alcohol and 1 min. in ammonia water to blue.

19. Run through graded alcohols to xylene and coverslip with permanent mounting media.

 

Last GLP modification 10/20/04:
Jennifer Casati
James R. Turk

 

Material List (top)

1. Surgipath X-tra Slides® 00210

3. Black and Decker HS2000 vegetable steamer

3. Dako Target Retrieval solution S1699

5. Dako S3306

6. A/B block Vector

8. Human and mouse caspase-3 p18 subunit

10. Dako, LSAB+ Kit, K0690

12. Streptavadin, Dako , LSAB+ Kit K0690

14. DAB Dako, K3466



Literature (top)

Apoptotic death of inflammatory cells in human atheroma.

Hyperglycemia-induced apoptosis in mouse myocardium: mitochondrial cytochrome C-mediated caspase-3 activation pathway.

Immunohistochemical localization of active caspase-3 in the mouse ovary: growth and atresia of small follicles.

Hypoxia-induced caspase-3 activation and DNA fragmentation in cortical neurons of newborn piglets: role of nitric oxide.

C5b-9 terminal complement complex assembly on apoptotic cells in human arterial wall with atherosclerosis.

Abnormal structural luteolysis in ovaries of the senescence accelerated mouse (SAM): expression of Fas ligand/Fas-mediated apoptosis signaling molecules in luteal cells.

Colocalization of DNA fragmentation and caspase-3 activation during atresia in pig antral follicles.

Caspase-3 and tissue factor expression in lipid-rich plaque macrophages: evidence for apoptosis as link between inflammation and atherothrombosis.

Apoptosis in normal lymphoid organs from healthy normal, conventional pigs at different ages detected by TUNEL and cleaved caspase-3 immunohistochemistry in paraffin-embedded tissues.

Myocardial apoptosis prevention by radical scavenging in patients undergoing cardiac surgery.