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Article #7734Re: Double label florescence
From: Natalie Bilyk
Date: Sun, 28 May 1995 00:00
Date: Sun, 28 May 1995 00:00
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> Texas Red and FITC works well for us. > > > I was wondering what you folks thought produed the best double label > > florescence for colocalization studies. I tried TRITC and FITC and > > thought we had a little bleeding through. Any other suggestions ??? > I would second that combination. We work with FITC and Texas Red and usually get very good results. One occaisional problem though - when scanning on dual green/red mode I sometimes come across a background staining that is excited by blue light but emits in the texas red wavelength. This forces me to abandon dual scanning and scan only for green or red emmission separately, which isn't always desirable. I'm curious to know if others have seen the same problem ? Natalia Bilyk Department of Anatomy and Human Biology University of Western Australia
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X-Google-Language: ENGLISH,ASCII-7-bit X-Google-Thread: 114d69,907ce7b26a228ae2 X-Google-Attributes: gid114d69,public From: Natalie Bilyk <nbilyk@UNIWA.UWA.EDU.AU> Subject: Re: Double label florescence Date: 1995/05/28 Message-ID: <Pine.ULT.3.90.950528171953.12667A-100000@uniwa.uwa.edu.au> X-Deja-AN: 103389990 sender: Confocal Microscopy List <CONFOCAL@UBVM.CC.BUFFALO.EDU> comments: Gated by NETNEWS@AUVM.AMERICAN.EDU content-type: TEXT/PLAIN; charset=US-ASCII mime-version: 1.0 newsgroups: bit.listserv.confocal