Team:Heidelberg/Notebook/Sensing Group/Notebook/5thweek

From 2008.igem.org

(Difference between revisions)
(Friday, 09/05/2008)
(Monday, 09/01/2008)
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== Monday, 09/01/2008 ==
== Monday, 09/01/2008 ==
* 1.selection for Fusion-1 and Fusion-2 cloning
* 1.selection for Fusion-1 and Fusion-2 cloning
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* the DNA of the colonies was extracted with MINIprep, and then screen with test digestion: PstI (Buffer3+BSA at 37)
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* the DNA of the colonies was extracted with MINIprep, and then screen with test digestion: PstI (NEBuffer 3 + BSA)
** for Fusion-1: if our insert is there: one band of 6101 bp if no inser: two bands: 4388 + 2213 bp  
** for Fusion-1: if our insert is there: one band of 6101 bp if no inser: two bands: 4388 + 2213 bp  
** for Fusion-2: if our insert is there: one band of 6122 bp if no inser: two bands: 4388 + 2213 bp
** for Fusion-2: if our insert is there: one band of 6122 bp if no inser: two bands: 4388 + 2213 bp

Revision as of 23:39, 26 October 2008

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Contents

Monday, 09/01/2008

  • 1.selection for Fusion-1 and Fusion-2 cloning
  • the DNA of the colonies was extracted with MINIprep, and then screen with test digestion: PstI (NEBuffer 3 + BSA)
    • for Fusion-1: if our insert is there: one band of 6101 bp if no inser: two bands: 4388 + 2213 bp
    • for Fusion-2: if our insert is there: one band of 6122 bp if no inser: two bands: 4388 + 2213 bp

PCR of LuxQ and two fusion protein constructs

  • Lyse V. harveyi for 5 min @ 99 °C
  • PCR with Phusion (template: supernatend of boiled V. harveyi (a), colony (b))
    • 5 min @ 98 °C || 20s @ 98 °C | 40s @ 58 °C | 1min @ 72 °C || 10 min @ 72 °C | 4 °C hold ( 35 cycles )
    • 35(34) µl H2O, 10 µl 5x HF, 0.5 µl each primer, 1µl Template, 2µl dNTPs, 1µl Phusion, 0(1) µl DMSO
  • PCR with Pfu
    • 3 min @ 94 °C || 45s @ 94 °C | 45s @ 58 °C | 2min @ 72 °C || 10 min @ 72 °C | 4 °C hold ( 35 cycles )
    • 40(39) µl H2O, 5 µl 10x Buffer, 0.5 µl each primer, 1µl Template, 2µl dNTPs, 1µl Pfu, 0(1) µl DMSO

NO PCR Product

Tuesday, 09/02/2008

  • PCR of LuxQ with taq-Polymerase with different DMSO concentrations (0 %, 5 %, 10 %). As template V. harveyi colonies and supernatant of cooked bacteria was used.

No PCR product

Wednesday, 09/03/2008

  • PCR of LuxP and LuxQ from Virio harveyi genome with Phusion Mastermix (without any annealing temp). Template: 0.2 µl V. harveyi culture incubated over night in LB(not 20% NaCl LB) at 37 °C.
    • result: no PCR product
  • PCR of LuxP and LuxQ from Vibrio harveyi genome with Fementas tag Mastermix
    • sample with normal Mg concentration (2 µg) and 6 µg Mg concentration
    • 5min @94°C ||30 sec @ 94°C | 30 sec @ 58°C | 2 min @ 72°C || 5 min @ 72°C | 4°C hold (30 cycles)
    • template is 0.2 ul water washed Vibrio harveyi cells.
    • result: see tomorrow (NO PRODUCT)
  • incubation of Vibrio harveyi from glycerol stock at 28 over night (medium is 20% NaCl LB)

Thursday, 09/04/2008

  • PCR of LuxP and LuxQ from Vibrio hayveyi genome with Tag Mastermix
    • template is 0.3 ul water washed Vibrio harveyi culture from 3rd September sample with DMSO(1 ul 100%DMSO) and without DMSO
    • Result: only byproduct
LuxQ PCR product

Friday, 09/05/2008

  • Cloning of LuxQ from day before into DH5a cells with standard protocols
  • Plated over weekend @ room temperature


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