*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Listers, I'm thinking of a possible tissue phantom to test the penetration depth of a multiphoton microscope. I would be thankful if you have any ideas/experience. Thank you in advance, Vladimir |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Vladimir, People who develop MRI sequences use tissue phantoms. I think the phantoms are agar based. If you have an MRI group close by, you could check with them. Best, Mollie -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Vladimir Gukassyan Sent: Friday, May 13, 2011 4:04 PM To: [hidden email] Subject: Tissue phantom for MP ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Listers, I'm thinking of a possible tissue phantom to test the penetration depth of a multiphoton microscope. I would be thankful if you have any ideas/experience. Thank you in advance, Vladimir Disclaimer: The materials in this e-mail are private and may contain Protected Health Information. Please note that e-mail is not necessarily confidential or secure. Your use of e-mail constitutes your acknowledgment of these confidentiality and security limitations. If you are not the intended recipient, be advised that any unauthorized use, disclosure, copying, distribution, or the taking of any action in reliance on the contents of this information is strictly prohibited. If you have received this e-mail in error, please immediately notify the sender via telephone or return e-mail. |
In reply to this post by Vladimir Ghukasyan-2
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I have successfully used a mixture of low melting temperature agarose with reconstituted powdered milk to make it turbid. The agarose concentration needs to be high enough that the gel does not jiggle when it solidifies. I don't have my notebook here so I can't tell you exactly what concentrations I used. You can either include Tetraspeck beads as point sources of fluorescence or a soluble fluorophore to get more uniform fluorescence. I put the mixture in a 35 mm dish and let it gel overnight before putting it on the scope. It is important to keep it hydrated. The samples don't keep forever even in the refrigerator because the milk spoils. So I make the samples fresh from stock solutions the day before I use them. Here is a reference from Peter So's lab describing a similar approach. Journal of Biomedical Optics 8(3), 450459 (July 2003) Kate |
In reply to this post by Vladimir Ghukasyan-2
|
Free forum by Nabble | Edit this page |