IGEM:University of East Anglia (UEA), Norwich, UK/2009/Notebook/NRP-UEA-Norwich iGEM/2013/07/25

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(Floor Two)
Current revision (14:30, 22 August 2013) (view source)
(Floor Two)
 
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|style="background-color: #EEE"|[[Image:igem-logo-150px.png|150px]]<span style="font-size:22px;"> iGEM Project name 1</span>
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|style="background-color: #EEE"|[[Image:igem-logo-150px.png|150px]]<span style="font-size:22px;"> Week 8</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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==Floor One==
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Streak purified all the isolated single Actinomycete colonies that appeared contaminated.
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Many single colony plates were removed due to lack of growth.
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All single colony plates were streaked to produce lawns (2 lawns per colony) in preparation for spore stocks.
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After the conjugation plates were incubated at 30 °C overnight, they were overlayed with antibiotics - 1 ml of sterile water, 20 ul nalidixic acid and 100 ul kanamycin per plate. The plates were then incubated again overnight at 30 °C.
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==Floor Two==
==Floor Two==
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The two ligation samples from the previous day were analysed by gel electrophoresis ''fig 2,'' alongside controls (2b2L and 3b1L) and the samples 2b and 2c from the 22nd July.
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[[Image:25 july.JPG|thumb|Fig 2: Analysis of Ligation reactions by gel electrophoresis. Lane 1 and 2 contain samples 1 and 2, lanes 3 and 4 controls, lane 5 and 6 samples from 22nd July (2b and 2c)repectively]]
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Transformation reactions were prepared using SOC media for the ligation reactions, J04450 plasmid and sample 3b from 11/07 (J04450 with Nde1 site).
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The membrane was retrieved from the shaker and washed with TBST and TBS solutions respectively for ten minutes. It was then incubated in Anti His HRP conjugate solution. After further washing the membrane was imaged using chemiluminescent detection. This gave no visible result.
The membrane was retrieved from the shaker and washed with TBST and TBS solutions respectively for ten minutes. It was then incubated in Anti His HRP conjugate solution. After further washing the membrane was imaged using chemiluminescent detection. This gave no visible result.

Current revision

Week 8 Main project page
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Floor One

Streak purified all the isolated single Actinomycete colonies that appeared contaminated.

Many single colony plates were removed due to lack of growth.

All single colony plates were streaked to produce lawns (2 lawns per colony) in preparation for spore stocks.

After the conjugation plates were incubated at 30 °C overnight, they were overlayed with antibiotics - 1 ml of sterile water, 20 ul nalidixic acid and 100 ul kanamycin per plate. The plates were then incubated again overnight at 30 °C.

Floor Two

The two ligation samples from the previous day were analysed by gel electrophoresis fig 2, alongside controls (2b2L and 3b1L) and the samples 2b and 2c from the 22nd July.

Fig 2: Analysis of Ligation reactions by gel electrophoresis. Lane 1 and 2 contain samples 1 and 2, lanes 3 and 4 controls, lane 5 and 6 samples from 22nd July (2b and 2c)repectively
Fig 2: Analysis of Ligation reactions by gel electrophoresis. Lane 1 and 2 contain samples 1 and 2, lanes 3 and 4 controls, lane 5 and 6 samples from 22nd July (2b and 2c)repectively

Transformation reactions were prepared using SOC media for the ligation reactions, J04450 plasmid and sample 3b from 11/07 (J04450 with Nde1 site).

The membrane was retrieved from the shaker and washed with TBST and TBS solutions respectively for ten minutes. It was then incubated in Anti His HRP conjugate solution. After further washing the membrane was imaged using chemiluminescent detection. This gave no visible result.



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