Team:NYMU-Taipei/ymip2.html
From 2012.igem.org
(Difference between revisions)
(4 intermediate revisions not shown) | |||
Line 64: | Line 64: | ||
<div id="ymi_header"> | <div id="ymi_header"> | ||
<div id="inner_header"> | <div id="inner_header"> | ||
- | <a href="https://2012.igem.org/Team:NYMU-Taipei"><img src="https://static.igem.org/mediawiki/2012/ | + | <a href="https://2012.igem.org/Team:NYMU-Taipei"><img src="https://static.igem.org/mediawiki/2012/1/15/Ymi_header1.jpg" border="0"></a> |
</div> | </div> | ||
</div> | </div> | ||
Line 79: | Line 79: | ||
<div id="ymi_left_column"> | <div id="ymi_left_column"> | ||
<div class="text_area" align="justify"> | <div class="text_area" align="justify"> | ||
- | <div class="title"> | + | <div class="title">Mesenchymal Stem Cells Culturing</div> |
<div align="left"> | <div align="left"> | ||
- | + | ||
</div> | </div> | ||
<div align="left"> | <div align="left"> | ||
Line 116: | Line 116: | ||
culturing</a></li> | culturing</a></li> | ||
<li><a title="Reprogramming of Somatic Cells into Stem & Separation of iPS cells" | <li><a title="Reprogramming of Somatic Cells into Stem & Separation of iPS cells" | ||
- | href="https://2012.igem.org/Team:NYMU-Taipei/ymip3.html">Reprogramming of Somatic | + | href="https://2012.igem.org/Team:NYMU-Taipei/ymip3.html">Reprogramming of Somatic Cells into Stem & Separation of iPS cells</a></li> |
- | Cells into Stem | + | |
- | Separation of iPS cells</a></li> | + | |
<li></li> | <li></li> | ||
<li></li> | <li></li> | ||
Line 134: | Line 132: | ||
href="https://2012.igem.org/Team:NYMU-Taipei/ymisf.html">Safety</a></li> | href="https://2012.igem.org/Team:NYMU-Taipei/ymisf.html">Safety</a></li> | ||
<li><a title="Collaboration with NTU" href="https://2012.igem.org/Team:NYMU-Taipei/ymico1.html">Collaboration with NTU</a></li> | <li><a title="Collaboration with NTU" href="https://2012.igem.org/Team:NYMU-Taipei/ymico1.html">Collaboration with NTU</a></li> | ||
- | <li><a title=" | + | |
- | + | <li><a title="NYMU Bioenergy Breakthrough" href="https://2012.igem.org/Team:NYMU-Taipei/ymibt.html">NYMU Bioenergy<br /> | |
+ | Breakthrough</a></li> | ||
<li><a title="Parts" | <li><a title="Parts" | ||
href="https://2012.igem.org/Team:NYMU-Taipei/ymiparts.html">Parts</a></li> | href="https://2012.igem.org/Team:NYMU-Taipei/ymiparts.html">Parts</a></li> |
Latest revision as of 17:34, 26 October 2012
Mesenchymal Stem Cells Culturing
- Mesenchymal stem cells from human umbilical cord were provided by Prof. Chun-Min Lo from National Yang Ming University.
- View cultures using a microscopy and after the cultures was full of the dish, remove the spent medium.
- Wash the cell monolayer with PBS and remove it.
- Add HyQTase(1ml per 25 cm2 of surface area) and incubate for 1 minutes.
- After making sure cells were detached, resuspend the cells with medium(more than 5 folds volume of HyQTase).
- Centrifuge under 2000 rpm, 5minutes, 25°C.
- Remove the supernatant and add 5 ml medium to suspend cells.
- Count the cells by Bright Line Counting Chamber. Subject the cell diversity to 104/ml
- Seed the cells for 104/well, 1ml/well in the 24-well plate.
- Until cells grow full of each well, do the coculturing experiment.