Team:Warsaw

From 2012.igem.org

(Difference between revisions)
 
(161 intermediate revisions not shown)
Line 1: Line 1:
-
<!-- *** What falls between these lines is the Alert Box!  You can remove it from your pages once you have read and understood the alert ***
+
{{Menu}}
 +
{{imageMove}}
<html>
<html>
-
<div id="box" style="width: 700px; margin-left: 137px; padding: 5px; border: 3px solid #000; background-color: #fe2b33;">
 
-
<div id="template" style="text-align: center; font-weight: bold; font-size: large; color: #f6f6f6; padding: 5px;">
 
-
This is a template page. READ THESE INSTRUCTIONS.
 
-
</div>
 
-
<div id="instructions" style="text-align: center; font-weight: normal; font-size: small; color: #f6f6f6; padding: 5px;">
 
-
You are provided with this team page template with which to start the iGEM season.  You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2009.igem.org/Help:Template/Examples">HERE</a>.
 
-
</div>
 
-
<div id="warning" style="text-align: center; font-weight: bold; font-size: small; color: #f6f6f6; padding: 5px;">
 
-
You <strong>MUST</strong> have all of the pages listed in the menu below with the names specified. PLEASE keep all of your pages within your teams namespace. 
 
-
</div>
 
-
</div>
 
-
</html>
 
-
|You can write a background of your team here.  Give us a background of your team, the members, etc.  Or tell us more about something of your choosing.
+
<body>
-
''Tell us more about your project.  Give us background.  Use this as the abstract of your project.  Be descriptive but concise (1-2 paragraphs)''
+
-
*** End of the alert box *** -->
+
<br clear="all" /><br clear="all" />
 +
<a href="https://static.igem.org/mediawiki/2012/c/c2/Igem_logo2_ver1.png"><img src="https://static.igem.org/mediawiki/2012/c/c2/Igem_logo2_ver1.png" width="200" alt="Warsaw Logo" border:"none" style="position:absolute; top:0px;left:0px;z-index:-10"/></a>
 +
<div class="box" style="background-color:rgba(200,200,200,0.5);z-index:-20;">
 +
<br clear="all" /><br clear="all" />
-
<!--- The Mission, Experiments --->
+
<p><hr/><br clear="all" /> Our project aims at creating a carrier bacteria, which could be used to deliver genes coding a chosen protein into the human cell. Some bacteria have a natural ability to enter eukaryotic cells. Our goal is to introduce this feature to bacteria which do not exhibit it normally, and which can be safely used to carry the “load” into an animal organism, and in the future the human body. As a result, thanks to the introduced gene, the eukaryotic cell has the ability to produce a new, normally not produced protein and the bacterial carrier decomposes after fulfilling its mission. This arrangement is not only an impressive scientific toy, but it also has important applications.</p><br />
-
{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="3" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
+
<br clear="all" />
-
!align="center"|[[Team:Warsaw|Home]]
+
<p>We will divide our project into two tasks: first will involve creating <i>Bacillus subtilis</i> strain with the ability to enter eukaryotic cell and subsequent lysis. From lysed <i>B.subtilis</i> cells GFP protein will be released so fluorescence measurement can be used to confirm success of the experiment. The second task is to create eukaryotic vector capable of replication and gene expression within host cell. Again, fluorescence measurement will be used to verify whether we've achieved our goal. Due to safety issues, we will not combine these two systems but only test them separately. One day it will be possible to use the whole system, but we must wait for some crucial problems to be dealt with.</p>
-
!align="center"|[[Team:Warsaw/Team|Team]]
+
<br clear="all" /><br clear="all" /><br clear="all" />
-
!align="center"|[https://igem.org/Team.cgi?year=2012&team_name=Warsaw Official Team Profile]
+
-
!align="center"|[[Team:Warsaw/Project|Project]]
+
-
!align="center"|[[Team:Warsaw/Parts|Parts Submitted to the Registry]]
+
-
!align="center"|[[Team:Warsaw/Modeling|Modeling]]
+
-
!align="center"|[[Team:Warsaw/Notebook|Notebook]]
+
-
!align="center"|[[Team:Warsaw/Safety|Safety]]
+
-
!align="center"|[[Team:Warsaw/Attributions|Attributions]]
+
-
|}
+
-
 
+
-
<br />
+
-
<div align="justify">
+
-
{|align="justify"
+
-
|Our project aims at creating a carrier bacteria, which could be used to deliver genes coding a chosen protein into the human cell. Some bacteria have a natural ability to enter eukaryotic cells. Our goal is to introduce this feature to bacteria which do not exhibit it normally, and which can be safely used to carry the “load” into an animal organism, and in the future the human body. As a result, thanks to the introduced gene, the eukaryotic cell has the ability to produce a new, normally not produced protein and the bacterial carrier decomposes after fulfilling its mission. This arrangement is not only an impressive scientific toy, but it also has important applications.<br />
+
-
We will divide our project into two tasks: first will involve creating
+
-
Bacillus subtilis strain with the ability to enter eukaryotic cell and
+
-
subsequent lysis. From lysed B.subtilis cells GFP protein will be
+
-
released so fluorescence measurement can be used to confirm success of
+
-
the experiment. The second task is to create eukaryotic vector capable
+
-
of replication and gene expression within host cell. Again,
+
-
fluorescence measurement will be used to verify whether we've achieved
+
-
our goal. Due to safety issues, we will not combine these two systems
+
-
but only test them separately. One day it will be possible to use the
+
-
whole system, but we must wait for some crucial problems to be dealt
+
-
with.
+
-
|[[Image:Warsaw_logo.png|200px|right|frame]]
+
-
|-
+
-
|
+
-
|[[Image:Warsaw_team.png|right|frame|Your team picture]]
+
-
|-
+
-
|
+
-
|}
+
</div>
</div>
 +
</body>
 +
</html>

Latest revision as of 23:10, 13 June 2013

Warsaw Team




Warsaw Logo





Our project aims at creating a carrier bacteria, which could be used to deliver genes coding a chosen protein into the human cell. Some bacteria have a natural ability to enter eukaryotic cells. Our goal is to introduce this feature to bacteria which do not exhibit it normally, and which can be safely used to carry the “load” into an animal organism, and in the future the human body. As a result, thanks to the introduced gene, the eukaryotic cell has the ability to produce a new, normally not produced protein and the bacterial carrier decomposes after fulfilling its mission. This arrangement is not only an impressive scientific toy, but it also has important applications.



We will divide our project into two tasks: first will involve creating Bacillus subtilis strain with the ability to enter eukaryotic cell and subsequent lysis. From lysed B.subtilis cells GFP protein will be released so fluorescence measurement can be used to confirm success of the experiment. The second task is to create eukaryotic vector capable of replication and gene expression within host cell. Again, fluorescence measurement will be used to verify whether we've achieved our goal. Due to safety issues, we will not combine these two systems but only test them separately. One day it will be possible to use the whole system, but we must wait for some crucial problems to be dealt with.