Team:Groningen/Notebook/5 August 2009

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It's my birthday!!! (Michael)

So cake it is....

Wet

GVP Cluster

DONE buy a nice cake and eat it ;)
TODO isolate plasmids from overnight precultures
DONE perform a ligation between cut vector and GVP fragment
DONE transform E.coli TOP10 competent cells with ligation product

Ligation

  • 2 uL Ligase buffer
  • 1 ul T4 Ligase
  • 8 uL plasmid pSB1AC3 digested with PstI and SpeI
  • 4 uL insert GVP restricted with XbaI and PstI

Incubate:

  • 25°C 30min.
  • kept on ice for 10min.

Tranformation

  • add 10uL of the pSB1AC3-GVP ligation product to 50uL competent E.coli TOP10 cells.

Incubate:

  • 30 min @ ice
  • 50 sec 42°C
  • 2 min @ ice
  • add 800uL LB-medium
  • incubate for 1 h at 37°C
  • plate on LB-amp50 plates

Transporters

GlpF Restriction, ligation and transformation as noted below.

Metal Accumulation

Restriction
10 ul GlpF PCR
1.5 ul Fast DigestBuffer
0.5 ul XbaI
0.5 ul PstI
10 ul ArsRMBP fusie (ligatie overnight 04-08-09)
1.5 ul Fast DigestBuffer
0.5 ul XbaI
0.5 ul PstI
11 ul psB1AC3 (30/07/09 nienke)
5 ul Fast DigestBuffer
2.5 ul XbaI
2.5 ul PstI
  • 37 30min
  • Inactivation on Gel
  • Extraction from gel


Ligation
2 uL Ligase buffer 16° 1h → 65° 10 min
1 ul T4 Ligase
11 uL GlpF digested with EcoRI and SpeI 42° 2 min →
11 uL psB1AC3 digested with EcoRi and SpeI
Tranformation
  • add 4 uL of the GlpFpsB1AC3 ligation mixture to 50uL competent e.coli top10 cells.

Incubate:

  • 30 min @ ice
  • 5 min 37°
  • 5min @ ice
  • add 800uL LB
  • incubate for 1 h at 37°
  • plate on LB-AMP plates

Dry

April
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May
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June
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29 30
July
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August
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31
September
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October
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November
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