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

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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"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}}
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==Lab==
==Lab==


Further digestions reactions were performed on the samples from last week as well as controls (original DNA) with Nde1 or Xba1 as well as EcoR1 & Pst1.
===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).
(We were not supposed to use EcoR1 but there was no enough Xba1).
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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.





Latest revision as of 23:04, 26 September 2017

Week Seven Main project page
Previous entry      Next entry

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.