Difference between revisions of "Team:SPSingapore/Notebook-Week-4"

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   <li><a href='https://2015.igem.org/Team:SPSingapore/Parts'><span>Parts</span></a></li>
 
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   <li class = 'active'><a href='https://2015.igem.org/Team:SPSingapore/Notebook'><span>Notebook</span></a></li>
 
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Revision as of 18:38, 12 September 2015


Research Notebook

Week 4 (14/6 - 20/6)

14th June 2015

Yi Han

• Miniprep of gfp plasmids, preparation of samples for sequencin

9th June 2015

Yi Han

• All gfp plasmids had a correct sequence
• Yun Ting kept glycerol stocok for all, and inoculation of 3mL of gfp3 into 100mL LB+amp for midiprep

10th June 2015

Yi Han & Yun Ting

• Midiprep of gfp plasmid
• PCR of gfp with KpnI-gfp and XhoI-gfp primers

11th June 2015

Yun Ting & Duy

• Nanodrop of gfp product → 595.5ng/ul
• RE digest of EsaR vector with KpnI/XHoI
• Gel electrophoreseis at 1000V for 30min
• Gel extraction: 3.9ng/ul and 6.9ng/ul for Esa fragment and GFP --> low yield

12th June 2015

Yun Ting

• Gel extraction using Promega binding solution to melt gel, followed by thermo scientific kit

Adrian

• Gel extraction optimisation
• Hypothesised that the Binding buffer has a problem/DNA does not bind to column
       1: 2X promega binding buffer volume
       2: Increase incubation time for binding to 5min
• Switch binding buffer to that of thermo scientific PCR purification kit
• Use sodium acetate if available? To facilitate stronger binding to column
Results:
       1: ~10ng/ul
       2: ~9ng/ul
•Further optimisation-> warm buffer, incubate for 5min
•Elute in 30/20ul smaller volumes

13th June 2015

Yi Han

1: Thermoscientific miniprep columns with 2XThermoscientific binding buffer
2: Thermoscientific PCR purification kit 2X buffer
3: Promega kit 2X buffer