Team:UT Dallas/Protocols
From 2011.igem.org
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<h2><span></span>Gel Electrophoresis Protocol</h2> | <h2><span></span>Gel Electrophoresis Protocol</h2> | ||
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- | <p><li type = "disk"><li type = "disk"><li type = "disk"><li type = "disk"><li type = "disk"><li type = "disk"><li type = "disk"><li type = "disk"><li type = "disk"><li type = "disk"><li type = "disk"><li type = "disk"></p></li> | + | <p><li type = "disk">Making a 1% agarose gel<li type = "disk">100mL 1X TBE buffer<li type = "disk">1g agarose<li type = "disk">microwave until agarose dissolves<li type = "disk">let mixture cool<li type = "disk">when cool add 8-10uL ethidium bromide<li type = "disk">stir gently, let cool<li type = "disk">pour into plate with comb already in place<li type = "disk">let harden<li type = "disk">Using the gel<li type = "disk">Add loading buffer to DNA (for 100uL DNA, add 20uL loading buffer)<li type = "disk">Load 2uL of DNA ladder into the gel<li type = "disk">Load DNA into the gel<li type = "disk">Run at 130V for 30min-1hr</p></li> |
<h2><span></span>Digestion Protocol</h2> | <h2><span></span>Digestion Protocol</h2> | ||
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Revision as of 16:22, 17 August 2011