Minnesota-experimental/2 March 2010

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(New page: '''Rachel''' Used PCR purification kit to purify digestion reaction. Performed ligation reaction with pucmod BB BglII/NotI vector and Eut MN BglII/NotI insert. Reaction was a 25 microlit...)
 
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'''Rachel'''
'''Rachel'''
Used PCR purification kit to purify digestion reaction.  Performed ligation reaction with pucmod BB BglII/NotI vector and Eut MN BglII/NotI insert.  Reaction was a 25 microliter reaction.
Used PCR purification kit to purify digestion reaction.  Performed ligation reaction with pucmod BB BglII/NotI vector and Eut MN BglII/NotI insert.  Reaction was a 25 microliter reaction.
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'''Tony and Matt'''
'''Tony and Matt'''
Concentrated Eut LK solution in speed-vac for sixteen minutes.  Eut LK solution digested with BglII/NotI (50 microliter reaction).
Concentrated Eut LK solution in speed-vac for sixteen minutes.  Eut LK solution digested with BglII/NotI (50 microliter reaction).
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'''Rachel and Ian'''
'''Rachel and Ian'''
Transformation of 15 microliters of ligation reaction from 3/2.  Plated on amp plates at 37 degree overnight.
Transformation of 15 microliters of ligation reaction from 3/2.  Plated on amp plates at 37 degree overnight.

Latest revision as of 03:38, 26 October 2010

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Rachel Used PCR purification kit to purify digestion reaction. Performed ligation reaction with pucmod BB BglII/NotI vector and Eut MN BglII/NotI insert. Reaction was a 25 microliter reaction.

Tony and Matt Concentrated Eut LK solution in speed-vac for sixteen minutes. Eut LK solution digested with BglII/NotI (50 microliter reaction).

Rachel and Ian Transformation of 15 microliters of ligation reaction from 3/2. Plated on amp plates at 37 degree overnight.