Hi Nicole, I don't know what kind of secondary antibody you are using, but we have had very good luck with the Alexa-Fluor secondaries. Often, when you go from an amplified chromagenic method (such as ABC) to a less-amplified staining method (such as with a fluorescently-labeled secondary), the primary antibody needs to be retitrated. Perhaps there is not enough amplification with a directly labeled seconday; you may need to add another lay or do additional amplification, such as with tyramide - we are having very good luck with Invitrogen's TSA kits that contain AlexaFluor dyes. The Perkin Elmer FITC-TSA kits also work well, but cost about 3X as much as Invitrogens.
If you send more information about your staining protocols, we could probably give you more specific advice. Kim Kim Merriam, MA, HT(ASCP)QIHC Cambridge, MA ________________________________ From: "Patten, Nicole (NIH/NIAAA) [F]" <[EMAIL PROTECTED]> To: histonet@lists.utsouthwestern.edu Sent: Wednesday, December 10, 2008 10:09:45 AM Subject: [Histonet] Primary works with ABC but not IF Hello- I am in a situation where my primary antibody works using the ABC method, but I do not see staining with immunofluorescence. My IF protocol works well with other antibodies so I do not know why it's not working with this particular antibody. Does anybody have any suggestions? I have considered using an avidin-Alexa Fluor conjugate but I am not sure if this is even possible (I am new to IHC) or how I would go about it. Would I need to first biotinylate my primary? Does anyone have any advice/protocols? Thanks! Any help would be greatly appreciated. Nicole Patten Post-Baccalaureate Fellow/IRTA NIAAA/National Institutes of Health _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
