Team:Calgary/10 May 2010

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<h1>University of Calgary</h1>
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'''Monday May 10, 2010'''
'''Monday May 10, 2010'''
Today, we learned the dimensions needed for a Polymerase Chain Reaction (PCR) Master Mix (which can be found in Lab Protocols) and attempted a PCR of our own to multiply the DNA. We used plasmids R0040 123502 (Red), R0040 GFP C2 (Blue) and R0040 GFP C1 (Yellow).  In addition to this, we used agarose gel electrophoresis to determine whether or not the DNA was indeed present.
Today, we learned the dimensions needed for a Polymerase Chain Reaction (PCR) Master Mix (which can be found in Lab Protocols) and attempted a PCR of our own to multiply the DNA. We used plasmids R0040 123502 (Red), R0040 GFP C2 (Blue) and R0040 GFP C1 (Yellow).  In addition to this, we used agarose gel electrophoresis to determine whether or not the DNA was indeed present.
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<h3>Check Another Date:</h3>
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|{{#calendar: query=preload=Team:Calgary/NotebookPreload | year=2010 | month=09 | title=Team:Calgary}}
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<a href="http://www.ucalgary.ca">&copy;2010 University of Calgary</a>
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Revision as of 21:24, 21 June 2010

University of Calgary

Monday May 10, 2010

Today, we learned the dimensions needed for a Polymerase Chain Reaction (PCR) Master Mix (which can be found in Lab Protocols) and attempted a PCR of our own to multiply the DNA. We used plasmids R0040 123502 (Red), R0040 GFP C2 (Blue) and R0040 GFP C1 (Yellow). In addition to this, we used agarose gel electrophoresis to determine whether or not the DNA was indeed present.

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