Materials & Methods > Core B >Immunohistochemical Staining for platelet derived growth factor receptor - beta (PDGFR-ß)
 

Turk Lab Standard Operating Procedure (SOP) for Immunohistochemical Staining for Tie-2

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 = rabbit polyclonal anti- amino acids 25-200 mapping within the extracellular domain of Tie-2 of human origin (source: SantaCruz, SC-9026)1:200 dilution. The antibody can be used on formalin-fixed paraffin-embedded tissue using pig ovary as positive control.

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 7/7/05:

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

8. Primary antibody, rabbit polyclonal anti- amino acids 25-200 mapping within the extracellular domain of Tie-2 of human origin

10. Dako, LSAB+ Kit, K0690

12. Streptavadin, Dako , LSAB+ Kit K0690

14. DAB Dako, K3466

Literature (top)

Angiopoietin-1, unlike angiopoietin-2, is incorporated into the extracellular matrix via its linker peptide region.

Effects of overexpression of CXCL10 (cytokine-responsive gene-2) on MA-10 mouse Leydig tumor cell steroidogenesis and proliferation.

Hao YH, Yong, HY, Murphy CN, Wax D, Samuel M, Rieke A, Lai L, Liu Z, Durtschi DC, Welbern VR, Price EM, McAllister RM, Turk JR, Laughlin MH, Prather RS, Rucker EB. Production of endothelial nitric oxide synthase (eNOS) over-expressing piglets. Transgenic Research, in press 6-20-06.