IGEM:University of East Anglia (UEA), Norwich, UK/2009/Notebook/NRP-UEA-Norwich iGEM/2013/07/15: Difference between revisions

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{|{{table}} width="800"
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|style="background-color: #EEE"|[[Image:igem-logo-150px.png|150px]]<span style="font-size:22px;"> iGEM Project name 1</span>
|style="background-color: #EEE"|[[Image:igem-logo-150px.png|150px]]<span style="font-size:22px;"> Week Seven</span>
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
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==Lab==
==Lab==
===Floor Two===


Further digestion reactions were performed on the samples from last week as well as controls (original DNA) with Nde1 or Xba1 as well as EcoR1 & Pst1.
Further digestion reactions were performed on the samples from last week as well as controls (original DNA) with Nde1 or Xba1 as well as EcoR1 & Pst1.
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After incubation samples were run on a gel to analyse them.
After incubation samples were run on a gel to analyse them.


===Floor One===
All soil samples received so far were numbered and decanted into uniform tubes (1-38).
Samples 1-38 were diluted from 10<sup>-1</sup> up to 10<sup>-10</sup>.
Soya flour mannitol (SFM) media was made in quantities of 6 x 500 ml, autoclaved for 1 hour then poured into plates to set.
Dilutions of 10<sup>-2</sup>, 10<sup>-4</sup>, 10<sup>-6</sup>, 10<sup>-8</sup> and 10<sup>-10</sup> of samples 1-11 were plated onto SFM + 500 μL per 500 ml of Nystatin (Ny) and Cyclohexamide (Cy).
Plates were incubated at 30°C for 7 days.
==Outreach==
Carried on e-mailing iGEm teams , but now focused on sediment after communications with Lab on floor 1.
Ben Thompson arrangements.
E-mailed iGEM contact (Nitwa ..) about the idea of an outreach registry, so that teams who are organizing a public engagement event (i.e. Forum) could have a infomrational resource pool to draw from, instead of starting from scrach each time.
Will follow up iGEM (Westminster) as they have a simliar project and may be interested in such a resource and collaborating in its construction.
Organized a meeting with Anne Osbourne (JIC) who spoke at this years SB6.0 SynBio conference. This is related to projects leading on from/inspired by iGEM and will focus on how iGEM bricks can be used in real research.




Revision as of 05:30, 25 September 2013

Week Seven <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

Lab

Floor Two

Further digestion reactions were performed on the samples from last week as well as controls (original DNA) with Nde1 or Xba1 as well as EcoR1 & Pst1.

(We were not supposed to use EcoR1 but there was no enough Xba1).

After incubation samples were run on a gel to analyse them.

Floor One

All soil samples received so far were numbered and decanted into uniform tubes (1-38).

Samples 1-38 were diluted from 10-1 up to 10-10.

Soya flour mannitol (SFM) media was made in quantities of 6 x 500 ml, autoclaved for 1 hour then poured into plates to set.

Dilutions of 10-2, 10-4, 10-6, 10-8 and 10-10 of samples 1-11 were plated onto SFM + 500 μL per 500 ml of Nystatin (Ny) and Cyclohexamide (Cy).

Plates were incubated at 30°C for 7 days.

Outreach

Carried on e-mailing iGEm teams , but now focused on sediment after communications with Lab on floor 1.

Ben Thompson arrangements.

E-mailed iGEM contact (Nitwa ..) about the idea of an outreach registry, so that teams who are organizing a public engagement event (i.e. Forum) could have a infomrational resource pool to draw from, instead of starting from scrach each time.

Will follow up iGEM (Westminster) as they have a simliar project and may be interested in such a resource and collaborating in its construction.

Organized a meeting with Anne Osbourne (JIC) who spoke at this years SB6.0 SynBio conference. This is related to projects leading on from/inspired by iGEM and will focus on how iGEM bricks can be used in real research.



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