SignalStain ® IHC Dual Staining Kit (AP, Rabbit, Red / HRP, Mouse, Brown)

Product Usage Information

Before executing a dual staining experiment, it is suggested to optimize each primary antibody for a 1 hour primary incubation. If the recommended antigen retrieval buffer is not the same for each antibody, then it is suggested to use EDTA for both antibodies.If the primary antibodies are not compatible with the same antibody diluent, then it is advised to perform the primary incubation and detection steps sequentially.After determination of the appropriate antibody dilution, it is recommended to test the order of chromogen development. There may be differences in the quality of the results depending upon which chromogen is developed first. This is accomplished by combining the primary antibodies on two slides for the primary incubation. One slide should have DAB developed first, followed by Vibrant Red.  The other slide should have Vibrant Red developed first, followed by DAB.  Review the slides and determine which order of chromogens yields optimal results.It is possible that an antibody’s performance will not be the same with all chromogens. If during the course of assay optimization it is determined that an antibody is not yielding ideal results, it is advised to test an alternate detection reagent/chromogen pair (e.g., SignalStain® IHC Dual Staining Kit (HRP, Rabbit, Brown / AP, Mouse, Red) #82456).Staining Overview:1. For paraffin-embedded sections, deparaffinize and hydrate tissue sections through xylenes or other clearing agents and graded alcohol series.2. Perform antigen retrieval as recommended by the primary antibody manufacturer. If the recommended antigen retrieval buffer is not the same for each antibody, then it is suggested to use EDTA for both antibodies.3. After washing, incubate sections in 3% H2O2 diluted in water for 10 minutes.4. Wash.5. Incubate sections for 30 minutes with blocking solution.6. Remove blocking solution from sections and incubate with rabbit and mouse primary antibodies diluted in the appropriate antibody diluent as recommended by the primary antibody manufacturer. If the primary antibodies are not compatible with the same antibody diluent, then it is advised to perform the primary incubation and detection steps sequentially.7. Wash.8. Incubate for 30 minutes with either the AP or HRP Boost Detection Reagent previously determined to be first.9. Wash.10. Apply the AP or HRP-compatible substrate, matching the Boost Detection Reagent used first, and develop for the recommended time. See Substrate Reagent Preparation below.11. Wash. 12. Incubate for 30 minutes with either the AP or HRP Boost Detection Reagent previously determined to be second.13. Wash.14. Apply the AP or HRP-compatible substrate, matching the Boost Detection Reagent used second, and develop for the recommended time. See Substrate Reagent Preparation below.15. Wash.16. Counterstain (optional), then clear and mount coverslips.