Melia Paizi |
*****
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. We need advice on how to improve adherence of satellite cells in culture to optical glass. We have tried matrigel, matrigel+polylysin, gelatin. Thank you! Melia Paizi, PhD Bioimaging Center Biomedical Core Facility The Bruce Rappaport Faculty of Medicine Technion - Israel Institute of Technology POB 9649 MS 9, Bat-Galim, Haifa 3109601 <https://www.google.co.il/maps/dir//Medical+School,+Haifa/@32.83426,34.983802,17z/data=!4m13!1m4!3m3!1s0x151dbbd0803422e7:0x4bc667f2ea55e771!2sMedical+School!3b1!4m7!1m0!1m5!1m1!1s0x151dbbd0803422e7:0x4bc667f2ea55e771!2m2!1d34.983802!2d32.83426?hl=en>, Israel Tel. +972-77-887-1106 <+972778871106>Fax. +972-4-829-5363 <+97248295363> [hidden email] bcf.technion.ac.il |
Chris Guerin-2 |
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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 Melia: We have had good results with Cell Tak (http://catalog2.corning.com/LifeSciences/en-CN/Shopping/ProductDetails.aspx?categoryname=&productid=354240%28Lifesciences%29 no commercial interests, just satisfied users). So far it sticks every cell type we have tried. One caveat though is that in inhibiting movement you might also be changing the physiology. Best wishes, Chris Guérin Manager, VIB Bio Imaging Core Ghent |
Maria Y. Boulina |
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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 Melia, I was just going to post the same: http://csmedia2.corning.com/LifeSciences/media/pdf/SPC-354240.pdf Cell-tak really works. Regards, Marcia Bulina 2016-05-18 9:10 GMT-04:00 Chris Guerin <[hidden email]>: > ***** > 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 Melia: > > We have had good results with Cell Tak ( > http://catalog2.corning.com/LifeSciences/en-CN/Shopping/ProductDetails.aspx?categoryname=&productid=354240%28Lifesciences%29 > no commercial interests, just satisfied users). So far it sticks every cell > type we have tried. One caveat though is that in inhibiting movement you > might also be changing the physiology. > > Best wishes, > > Chris Guérin > Manager, VIB Bio Imaging Core Ghent > |
Smith, Benjamin E. |
In reply to this post by Melia Paizi
There are two ways to try matrigel, either as a slab or as a thin film. In my experience, the thin-film worked very well for many different cell types. Basically, you dilute the matrigel 1:10 and apply a thin layer to the cover slip and then allow it to completely air dry. If the growth factors in matrigel prove to be altering the cell behavior, collagen is another option.
-Ben Smith ________________________________________ From: Confocal Microscopy List <[hidden email]> on behalf of Melia Paizi <[hidden email]> Sent: Wednesday, May 18, 2016 5:57:21 AM To: [hidden email] Subject: Adherence of satellite cells to glass ***** 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. We need advice on how to improve adherence of satellite cells in culture to optical glass. We have tried matrigel, matrigel+polylysin, gelatin. Thank you! Melia Paizi, PhD Bioimaging Center Biomedical Core Facility The Bruce Rappaport Faculty of Medicine Technion - Israel Institute of Technology POB 9649 MS 9, Bat-Galim, Haifa 3109601 <https://www.google.co.il/maps/dir//Medical+School,+Haifa/@32.83426,34.983802,17z/data=!4m13!1m4!3m3!1s0x151dbbd0803422e7:0x4bc667f2ea55e771!2sMedical+School!3b1!4m7!1m0!1m5!1m1!1s0x151dbbd0803422e7:0x4bc667f2ea55e771!2m2!1d34.983802!2d32.83426?hl=en>, Israel Tel. +972-77-887-1106 <+972778871106>Fax. +972-4-829-5363 <+97248295363> [hidden email] bcf.technion.ac.il |
In reply to this post by Melia Paizi
*****
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 Melia, we have had good success sticking post-culture, fixed mast cells to glass by pretreating the glass with alcian blue. The idea came from: http://onlinelibrary.wiley.com/doi/10.1002/%28SICI%291097-0320%2820000401%2939:4%3C295::AID-CYTO7%3E3.0.CO;2-X/full We do this to avoid flattening cells by cytospinning, especially where we are attempting uptake studies, where imaging the cells in the round makes it much easier to assess whether a fed probe is on or in. I don't know if you could do this under sterile conditions for long term live imaging though, as, from memory, if you try to filter sterilise alcian blue solutions, you end up with a colourless filtrate and a blocked filter! DAJ David A Johnston, Biomedical Imaging Unit, Faculty of Medicine, University of Southampton, Mailpoint 12, Level B, Lab and Path Block, Southampton General Hospital, Tremona Road, Southampton SO16 6YD |
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