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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi everybody, Has anybody tested TagRFP, and eventually compared it to mCherry? It seems from the literature that TagRFP is much brighter. Is it also photostable? On our scopes, we have filters matching both proteins, we just want to pick up the "best" one... Thanks in advance for your feedback! Laurent. ___________________________ Laurent Gelman, PhD Friedrich Miescher Institut Facility for Advanced Imaging and Microscopy Head of Light Microscopy WRO 1066.2.16 Maulbeerstrasse 66 CH-4058 Basel +41 (0)79 618 73 69 |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** You'll want the turbo variant, which is critical for photostability. In our hands that has been much brighter than mCherry. However, we have been restricted to a 568 laser. Sent from iPhone On May 23, 2011, at 10:30 AM, "Gelman, Laurent" <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Hi everybody, > > > > Has anybody tested TagRFP, and eventually compared it to mCherry? > > > > It seems from the literature that TagRFP is much brighter. Is it also > photostable? On our scopes, we have filters matching both proteins, we > just want to pick up the "best" one... > > > > Thanks in advance for your feedback! > > > > Laurent. > > > > > > ___________________________ > > Laurent Gelman, PhD > > Friedrich Miescher Institut > > Facility for Advanced Imaging and Microscopy > > Head of Light Microscopy > > WRO 1066.2.16 > > Maulbeerstrasse 66 > > CH-4058 Basel > > +41 (0)79 618 73 69 > > |
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I tested TagRFP-T in yeast recently and found that it was less bright than mCherry. However, there could be issues arising from different codon usage in the two constructs - it wasn't as carefully controlled an experiment as could be done. Kurt On 5/23/2011 8:57 AM, Bunnell, Stephen C. wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > You'll want the turbo variant, which is critical for photostability. In our hands that has been much brighter than mCherry. However, we have been restricted to a 568 laser. > > Sent from iPhone > > On May 23, 2011, at 10:30 AM, "Gelman, Laurent"<[hidden email]> wrote: > >> ***** >> To join, leave or search the confocal microscopy listserv, go to: >> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >> ***** >> >> Hi everybody, >> >> >> >> Has anybody tested TagRFP, and eventually compared it to mCherry? >> >> >> >> It seems from the literature that TagRFP is much brighter. Is it also >> photostable? On our scopes, we have filters matching both proteins, we >> just want to pick up the "best" one... >> >> >> >> Thanks in advance for your feedback! >> >> >> >> Laurent. >> >> >> >> >> >> ___________________________ >> >> Laurent Gelman, PhD >> >> Friedrich Miescher Institut >> >> Facility for Advanced Imaging and Microscopy >> >> Head of Light Microscopy >> >> WRO 1066.2.16 >> >> Maulbeerstrasse 66 >> >> CH-4058 Basel >> >> +41 (0)79 618 73 69 >> >> |
In reply to this post by lgelman
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Laurent, It depends on the laser you've got. TagRFP absorbs at ~560, whereas mCherry is at ~590. My experience is TagRFP is a lot more brighter and stable than mCherry at 561nm. Soren ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi everybody, Has anybody tested TagRFP, and eventually compared it to mCherry? It seems from the literature that TagRFP is much brighter. Is it also photostable? On our scopes, we have filters matching both proteins, we just want to pick up the "best" one... Thanks in advance for your feedback! Laurent. ___________________________ Laurent Gelman, PhD Friedrich Miescher Institut Facility for Advanced Imaging and Microscopy Head of Light Microscopy WRO 1066.2.16 Maulbeerstrasse 66 CH-4058 Basel +41 (0)79 618 73 69 ________________________________ Advertência/Warning Esta mensagem (incluindo eventuais ficheiros anexos) pode conter informação confidencial ou privilegiada. Se não for o destinatário pretendido, por favor contacte o remetente por e-mail e apague a mensagem do seu sistema informático. This message and any files transmitted with it may contain confidential information or privileged material. If you are not the intended recipient, please notify the sender by e-mail and delete this message from your system. |
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