*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** I have a user who would like to do a multiphoton experiment with dipping lenses with rhodamine dye in the dipping solution. Would this be a problem for the dipping lenses? I would assume as long as the lens is cleaned well after use it should be fine. Anyone think otherwise? Sincerely, Claire |
Rosemary.White |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Hi Claire, It’s happened to us by accident! The lenses come up fine, though unless you clean very thoroughly, the ceramic tip may remain slightly pink. cheers, Rosemary On 15/2/17, 2:20 pm, "Confocal Microscopy List on behalf of Claire Brown, Dr." <[hidden email] on behalf of [hidden email]> wrote: ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** I have a user who would like to do a multiphoton experiment with dipping lenses with rhodamine dye in the dipping solution. Would this be a problem for the dipping lenses? I would assume as long as the lens is cleaned well after use it should be fine. Anyone think otherwise? Sincerely, Claire |
In reply to this post by Claire Brown
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Claire My main concern is the type of bond or sealant used to bond the lower element in the lens or the material the barrel of the lens tube is made of. The bond or tube could have a surface porosity where dye could become bound. The glass will clean but residual dye elsewhere could be a problem. Dan > On Feb 14, 2017, at 10:20 PM, Claire Brown, Dr. <[hidden email]> wrote: > > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > Post images on http://www.imgur.com and include the link in your posting. > ***** > > I have a user who would like to do a multiphoton experiment with dipping lenses with rhodamine dye in the dipping solution. > Would this be a problem for the dipping lenses? > I would assume as long as the lens is cleaned well after use it should be fine. > > Anyone think otherwise? > > Sincerely, > > Claire Dan Focht Bioptechs, Inc. 3560 Beck Rd. Butler PA 16002 V724-282-7145 F724-282-0745 Toll Free 877 lIVE-CELL (548-3235) [hidden email] |
Steffen Dietzel |
In reply to this post by Claire Brown
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Well, I used Hoechst once to stain nuclei in a tissue. Despite cleaning of the dipping objective, we did see nuclear staining in subsequent experiments. So yes, the lens may carry over a dye. Whether or not this is a problem depends, of course. At the time it didn't bother us too much and eventually the effect was lost. It might help to keep the lens in a large water bath for some hours (with flow?), to speed up the wash out. Steffen Am 15.02.2017 um 04:20 schrieb Claire Brown, Dr.: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > Post images on http://www.imgur.com and include the link in your posting. > ***** > > I have a user who would like to do a multiphoton experiment with dipping lenses with rhodamine dye in the dipping solution. > Would this be a problem for the dipping lenses? > I would assume as long as the lens is cleaned well after use it should be fine. > > Anyone think otherwise? > > Sincerely, > > Claire > -- ------------------------------------------------------------ Steffen Dietzel, PD Dr. rer. nat Ludwig-Maximilians-Universität München Biomedical Center (BMC) Head of the Core Facility Bioimaging Großhaderner Straße 9 D-82152 Planegg-Martinsried Germany http://www.bioimaging.bmc.med.uni-muenchen.de |
In reply to this post by Claire Brown
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** We've done it. With rhodamine dextran. No problems. Recommend keeping lens hydrated between samples. ========================================================================= Michael Cammer, Microscopy Core & Skirball Institute, NYU Langone Medical Center Cell: 914-309-3270 Office: Skirball 2nd Floor main office, back right http://ocs.med.nyu.edu/microscopy & http://microscopynotes.com/ -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Claire Brown, Dr. Sent: Tuesday, February 14, 2017 10:20 PM To: [hidden email] Subject: Dye Solution with Dipping lens ***** To join, leave or search the confocal microscopy listserv, go to: https://urldefense.proofpoint.com/v2/url?u=http-3A__lists.umn.edu_cgi-2Dbin_wa-3FA0-3Dconfocalmicroscopy&d=DQIFAg&c=j5oPpO0eBH1iio48DtsedbOBGmuw5jHLjgvtN2r4ehE&r=oU_05LztNstAydlbm5L5GDu_vAdjXk3frDLx_CqKkuo&m=YPfxvls2n3xW_tgBTkJXum1W5vWGxLO-IQiYDeKDKNE&s=zHBltq-MhZgsf8Hi7XS-UE8-0-UZUa8slDTnKDZEPcw&e= Post images on https://urldefense.proofpoint.com/v2/url?u=http-3A__www.imgur.com&d=DQIFAg&c=j5oPpO0eBH1iio48DtsedbOBGmuw5jHLjgvtN2r4ehE&r=oU_05LztNstAydlbm5L5GDu_vAdjXk3frDLx_CqKkuo&m=YPfxvls2n3xW_tgBTkJXum1W5vWGxLO-IQiYDeKDKNE&s=2mh7NRSiorEcJzfbrXqCsChwzXHxmPvcJNojPfEUqVk&e= and include the link in your posting. ***** I have a user who would like to do a multiphoton experiment with dipping lenses with rhodamine dye in the dipping solution. Would this be a problem for the dipping lenses? I would assume as long as the lens is cleaned well after use it should be fine. Anyone think otherwise? Sincerely, Claire ------------------------------------------------------------ This email message, including any attachments, is for the sole use of the intended recipient(s) and may contain information that is proprietary, confidential, and exempt from disclosure under applicable law. Any unauthorized review, use, disclosure, or distribution is prohibited. If you have received this email in error please notify the sender by return email and delete the original message. Please note, the recipient should check this email and any attachments for the presence of viruses. The organization accepts no liability for any damage caused by any virus transmitted by this email. ================================= |
Craig Brideau |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy Post images on http://www.imgur.com and include the link in your posting. ***** Some dyes can be cleared from the cone with a bath in vinegar if you notice any persistence. I have used this for nile red. Craig On Feb 15, 2017 7:59 AM, "Cammer, Michael" <[hidden email]> wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > Post images on http://www.imgur.com and include the link in your posting. > ***** > > We've done it. With rhodamine dextran. No problems. Recommend keeping > lens hydrated between samples. > > ========================================================================= > Michael Cammer, Microscopy Core & Skirball Institute, NYU Langone Medical > Center > Cell: 914-309-3270 Office: Skirball 2nd Floor main office, > back right > http://ocs.med.nyu.edu/microscopy & > http://microscopynotes.com/ > > > -----Original Message----- > From: Confocal Microscopy List [mailto:[hidden email]] > On Behalf Of Claire Brown, Dr. > Sent: Tuesday, February 14, 2017 10:20 PM > To: [hidden email] > Subject: Dye Solution with Dipping lens > > ***** > To join, leave or search the confocal microscopy listserv, go to: > https://urldefense.proofpoint.com/v2/url?u=http-3A__lists. > umn.edu_cgi-2Dbin_wa-3FA0-3Dconfocalmicroscopy&d=DQIFAg&c= > j5oPpO0eBH1iio48DtsedbOBGmuw5jHLjgvtN2r4ehE&r=oU_05LztNstAydlbm5L5GDu_ > vAdjXk3frDLx_CqKkuo&m=YPfxvls2n3xW_tgBTkJXum1W5vWGxLO- > IQiYDeKDKNE&s=zHBltq-MhZgsf8Hi7XS-UE8-0-UZUa8slDTnKDZEPcw&e= > Post images on https://urldefense.proofpoint.com/v2/url?u=http-3A__www. > imgur.com&d=DQIFAg&c=j5oPpO0eBH1iio48DtsedbOBGmuw5jHLjgvtN2r4ehE&r=oU_ > 05LztNstAydlbm5L5GDu_vAdjXk3frDLx_CqKkuo&m=YPfxvls2n3xW_ > tgBTkJXum1W5vWGxLO-IQiYDeKDKNE&s=2mh7NRSiorEcJzfbrXqCsChwzXHxmP > vcJNojPfEUqVk&e= and include the link in your posting. > ***** > > I have a user who would like to do a multiphoton experiment with dipping > lenses with rhodamine dye in the dipping solution. > Would this be a problem for the dipping lenses? > I would assume as long as the lens is cleaned well after use it should be > fine. > > Anyone think otherwise? > > Sincerely, > > Claire > > ------------------------------------------------------------ > This email message, including any attachments, is for the sole use of the > intended recipient(s) and may contain information that is proprietary, > confidential, and exempt from disclosure under applicable law. Any > unauthorized review, use, disclosure, or distribution is prohibited. If you > have received this email in error please notify the sender by return email > and delete the original message. Please note, the recipient should check > this email and any attachments for the presence of viruses. The > organization accepts no liability for any damage caused by any virus > transmitted by this email. > ================================= > |
Free forum by Nabble | Edit this page |