Atul Anand |
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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. ***** Dear All, I am struggling to capture DIC or bright field images our LSM 700 microscopy (ZEN software). Please help and suggest for this. Thanks in advance. Have a nice day Best Regards Atul Venlig hilsen ******************************************** Atul Anand PhD student Centre for Autophagy, Recycling and Disease (CARD) Cell Death and Metabolism Danish Cancer Society Research Center Strandboulevarden 49 DK-2100 Copenhagen Denmark Tel: +45-71 83 57 83 |
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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, You should have a transmission PMT ? T-PMT Just clic on it ! Regards |
Göran Månsson |
In reply to this post by Atul Anand
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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. ***** Dear Atul, Apart from activating the detector for transmitted light (T-PMT) you may also have to manually switch the light path from the halogen light source (to see transmitted channel in the eye pieces) to the T-PMT. (This is in case you have a manual system). For good quality transmitted channel you must of course set the Kohler illumination properly. Regards Göran -----Ursprungligt meddelande----- Från: Confocal Microscopy List [mailto:[hidden email]] För Atul Anand Skickat: den 12 februari 2015 10:37 Till: [hidden email] Ämne: DIC or bright field images on LSM 700 ***** 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. ***** Dear All, I am struggling to capture DIC or bright field images our LSM 700 microscopy (ZEN software). Please help and suggest for this. Thanks in advance. Have a nice day Best Regards Atul Venlig hilsen ******************************************** Atul Anand PhD student Centre for Autophagy, Recycling and Disease (CARD) Cell Death and Metabolism Danish Cancer Society Research Center Strandboulevarden 49 DK-2100 Copenhagen Denmark Tel: +45-71 83 57 83 |
Vickie Frohlich |
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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. ***** Are you certain that you have the polarizer in the condenser set to the proper position for imaging DIC via laser illumination. In the inverted scopes the proper position is 90 degrees off form that used for viewing by eye. Vickie -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Göran Månsson Sent: Thursday, February 12, 2015 6:50 AM To: [hidden email] Subject: SV: DIC or bright field images on LSM 700 ***** 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. ***** Dear Atul, Apart from activating the detector for transmitted light (T-PMT) you may also have to manually switch the light path from the halogen light source (to see transmitted channel in the eye pieces) to the T-PMT. (This is in case you have a manual system). For good quality transmitted channel you must of course set the Kohler illumination properly. Regards Göran -----Ursprungligt meddelande----- Från: Confocal Microscopy List [mailto:[hidden email]] För Atul Anand Skickat: den 12 februari 2015 10:37 Till: [hidden email] Ämne: DIC or bright field images on LSM 700 ***** 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. ***** Dear All, I am struggling to capture DIC or bright field images our LSM 700 microscopy (ZEN software). Please help and suggest for this. Thanks in advance. Have a nice day Best Regards Atul Venlig hilsen ******************************************** Atul Anand PhD student Centre for Autophagy, Recycling and Disease (CARD) Cell Death and Metabolism Danish Cancer Society Research Center Strandboulevarden 49 DK-2100 Copenhagen Denmark Tel: +45-71 83 57 83 |
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