User:University of Washington/25 July 2008

From 2008.igem.org

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(LuxR from AraC and TetR)
(LuxR from AraC and TetR)
 
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-Received primers to biobrick Elowitz's plasmid.
-Received primers to biobrick Elowitz's plasmid.
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-Did PCR amplification on Elowitz's plasmid.
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-Did PCR amplification on Elowitz's plasmid (from 4 minipreps).
*Reaction Set-Up
*Reaction Set-Up
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- Good news. Ran gel on PCR product. Expected 172 bp. Got fragments shorter than 500 kb. =]
 +
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- Bad news. Sequencing result for second trial Quikchange came. The sequences did not show any mutation. =[
==LuxR from pLac==
==LuxR from pLac==

Latest revision as of 00:06, 26 July 2008

LuxR from AraC and TetR

-Received primers to biobrick Elowitz's plasmid.

-Did PCR amplification on Elowitz's plasmid (from 4 minipreps).

  • Reaction Set-Up
reagentsamount per reaction(ul)
sterile dH2O34.5
buffer for Taq (-MgCl2)5
10 mM dNTPs1
MgCl22
F primer(#436)2.5
R primer(#436)2.5
Taq0.5
DNA template2
  • Thermocycling
SegmentCyclesTemperatureTime
1195°C1 minute
23095°C30 seconds
50°C1 min
72°C1 min
3172°C7 minutes
4-4°Cinfinite

- Good news. Ran gel on PCR product. Expected 172 bp. Got fragments shorter than 500 kb. =]

- Bad news. Sequencing result for second trial Quikchange came. The sequences did not show any mutation. =[

LuxR from pLac

-R0010+E0420 transformed cells' DNA was sent in for sequencing.

-Glycerol stock of DH5a+lacq strain made.

-One aliquot of electrocompetent DH5a+lacq cells were made.

-Sequence of part I0462 from the 2007 plates was received back and found to be the incorrect sequence. Sent an email to igem hq requesting bacterial stab of part I0462.


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