840:153g:Projects/project23/2012/09/27: Difference between revisions

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Cloning of the OmcF gene</span>
|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> Cloning of the OmcF gene</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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==Entry title==
==Entry title==
* We began the Transformation process of adding our vector, psB2k3 to E.coli
* We began the Transformation process of adding our vector, psB2k3, with promoter BBa_I0500 to E.coli
* We successfully plated our transformed E. coli onto three different types of media and let incubate and then refrigerate
* We successfully plated our transformed E. coli onto three different types of media, We created two types of controls, positive and negative. For the positive control we transformed an AmpR vector into the E.coli to make sure there was not a problem with our bacteria being able to uptake the vectors and then plated in on an AmpR LB media plate and onto a Kanamycin plate to test for the effectiveness of the Kanamycin. For our negative control, we transformed just water into our E.coli to test the growth ability of our E.coli to confirm that no issues with the bacteria itself exists. We plated this on regular LB media. Lastly we plated our KanR vector+E.coli onto Kanamycin plates.  and let incubate and then refrigerate
* On Thursday, we received our bacteria and began working on the DNA extraction
* On Thursday,our bacteria was shipped from the University of Massachusetts and thus we began working on the DNA extraction
* We were able to make it through the first have of the extraction process, adding our buffer, spinning it down, removing the supernatant, adding TE, SDS, and EDTA, incubated it, added isopropanol and let store until the next class period
* We were able to make it through the first half of the extraction process, adding our buffer, removing the supernatant, adding TE, SDS, and EDTA, incubated it, added isopropanol and let store until the next class period




Latest revision as of 22:04, 26 September 2017

Cloning of the OmcF gene Main project page
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Entry title

  • We began the Transformation process of adding our vector, psB2k3, with promoter BBa_I0500 to E.coli
  • We successfully plated our transformed E. coli onto three different types of media, We created two types of controls, positive and negative. For the positive control we transformed an AmpR vector into the E.coli to make sure there was not a problem with our bacteria being able to uptake the vectors and then plated in on an AmpR LB media plate and onto a Kanamycin plate to test for the effectiveness of the Kanamycin. For our negative control, we transformed just water into our E.coli to test the growth ability of our E.coli to confirm that no issues with the bacteria itself exists. We plated this on regular LB media. Lastly we plated our KanR vector+E.coli onto Kanamycin plates. and let incubate and then refrigerate
  • On Thursday,our bacteria was shipped from the University of Massachusetts and thus we began working on the DNA extraction
  • We were able to make it through the first half of the extraction process, adding our buffer, removing the supernatant, adding TE, SDS, and EDTA, incubated it, added isopropanol and let store until the next class period


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