Yep, Definitely an issue.
You can easily stain the IPX slides with H&E, though the discernibility of the cells and tissue structure with the H&E will depend on the degree of DAB product laid down (eg I would expect it to be difficult with a Vimentin IPX compared to a CD15). (Grosset, A. A., Loayza-Vega, K., Adam-Granger, É., Birlea, M., Gilks, B., Nguyen, B., ... & Trudel, D. (2017). Hematoxylin and Eosin Counterstaining Protocol for Immunohistochemistry Interpretation and Diagnosis. Applied immunohistochemistry & molecular morphology: AIMM.) As for doing another IPX on the existing IPX stained section (with DAB as the chromogen), you will have to use a different label (eg alkaline phosphatase). The result will depend on the cell compartment the two antigens exist. If the DAB is nuclear, then a cytoplasm or cytoplasmic membrane localisation with the Alk Phosphatase will work. If both antigens are cytoplasmic, then you will not see co-localisation in the same cell since the DAB will prevent any antibody binding in the same compartment. Assuming the above is good, then since the antigen retrieval tends to reverse over time, I would include a short retrieval before the second antibody. Now after all that, I hope the section stays on the slide! Regards Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA) Principal Scientist, the Children's Hospital at Westmead Adjunct Fellow, School of Medicine, University of Western Sydney Tel: 612 9845 3306 Fax: 612 9845 3318 Pathology Department the children's hospital at westmead Cnr Hawkesbury Road and Hainsworth Street, Westmead Locked Bag 4001, Westmead NSW 2145, AUSTRALIA -----Original Message----- From: Curt via Histonet [mailto:histonet@lists.utsouthwestern.edu] Sent: Friday, 4 January 2019 4:05 AM To: histonet@lists.utsouthwestern.edu Subject: [Histonet] IHC-H&E-IHC HELP... Need help before I turn a mistake into an irreparable mistake... We have some unstained slides that were supposed to get stained with H&E but my guy stained them with IHC. It's complicated, we received slides and a block, the block was for IHC, the unstained slides were for H&E, he inverted the process) The point is, now the unstained slides are stained with IHC... I know we cannot destain the IHC but we can simply run and H&E over them... the real question I have is subsequent to the H&E... this pathologist generally likes to see the H&E then order IHC on them based on what he sees (we only have these few unstained slides, don't have blocks to recut)... So the question is... if we've already run IHC, then followed that with and H&E, can we return to run IHC on the slides again? would you want to skip any pre-treatment, antigen retrieval???? I don't see this working too well myself, if they're already stained with DAB, that would be present on the second stain... Thoughts? Thanks for your help. Curt CONFIDENTIALITY NOTE: The information transmitted, including attachments, is intended only for the person(s) or entity to which it is addressed and may contain confidential and/or privileged material. Any review, retransmission, dissemination or other use of, or taking of any action in reliance upon this information by persons or entities other than the intended recipient is prohibited. If you received this in error, please contact the sender and destroy any copies of this information. _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet This message is intended for the addressee named and may contain confidential information. If you are not the intended recipient, please delete it and notify the sender. Views expressed in this message are those of the individual sender, and are not necessarily the views of NSW Health or any of its entities. _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
