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Team:ATOMS-Turkiye/Interlab-Study
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<h1>Interlab-Study</h1> | <h1>Interlab-Study</h1> | ||
| - | <li>This year, our team was involved in the international scientific experiment study organized by iGEM and declared on the main page of the iGEM website. Considering the promising nature of intensifying international collaboration and its ability to obtain more significant and accurate results, we were delighted to take part in this study and organization. </li> | + | <ul><li>This year, our team was involved in the international scientific experiment study organized by iGEM and declared on the main page of the iGEM website. Considering the promising nature of intensifying international collaboration and its ability to obtain more significant and accurate results, we were delighted to take part in this study and organization. </li> |
<li>It is important to remind ourselves of the interlab measurement study basics and the expectations from each lab before explaining the kind of process we carried out and what we have accomplished by joining this study. </li> | <li>It is important to remind ourselves of the interlab measurement study basics and the expectations from each lab before explaining the kind of process we carried out and what we have accomplished by joining this study. </li> | ||
| - | <li> As it is summarized on the iGEM Measurement Study page, participating team must fulfill these requirements:</li> | + | <li> As it is summarized on the iGEM Measurement Study page, participating team must fulfill these requirements:</li></ul> |
<div style="text-indent:35px">1. Designing a wiki page about the contribution and the achievements of study.</div> | <div style="text-indent:35px">1. Designing a wiki page about the contribution and the achievements of study.</div> | ||
<div style="text-indent:35px">2. Constructing the particular BioBricks defined clearly on the page. | <div style="text-indent:35px">2. Constructing the particular BioBricks defined clearly on the page. | ||
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(The results are sent to iGEM HQ and also shown below.)</div> | (The results are sent to iGEM HQ and also shown below.)</div> | ||
<div style="text-indent:35px">4. Submitting these data through Interlab Study form. | <div style="text-indent:35px">4. Submitting these data through Interlab Study form. | ||
| - | (To check out our form: <a href=" | + | (To check out our form: <a href="https://static.igem.org/mediawiki/2014/7/7d/IGEM_Interlab_Study_Worksheet.pdf"> here </a>)</div> |
<li>Due to achieving all these requirements, we began to work in parallel with the identified tasks:</li> | <li>Due to achieving all these requirements, we began to work in parallel with the identified tasks:</li> | ||
<div style="text-indent:35px">a. Existing device: BBa_I20260 (J23101-B0032-E0040-B0015) in the pSB3K3 vector.</div> | <div style="text-indent:35px">a. Existing device: BBa_I20260 (J23101-B0032-E0040-B0015) in the pSB3K3 vector.</div> | ||
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<li>In order to present the results of each part, we separated the experimental approach into four sections:</li> | <li>In order to present the results of each part, we separated the experimental approach into four sections:</li> | ||
<div style="text-indent:35px">- PRE-EXPERIMENTAL PREPARATION: | <div style="text-indent:35px">- PRE-EXPERIMENTAL PREPARATION: | ||
| - | We planned to use E.coli BL21 (DE3) strain in order to obtain high amounts of protein yield enabling us to calculate the fluorescence emission. Prior for the cloning process, we prepared competent cells using this protocol. LINK</li> | + | We planned to use E.coli BL21 (DE3) strain in order to obtain high amounts of protein yield enabling us to calculate the fluorescence emission. Prior for the cloning process, we prepared competent cells using this protocol. LINK</li></div> |
<div style="text-indent:35px">- FOR CLONING: BBA_I20260 | <div style="text-indent:35px">- FOR CLONING: BBA_I20260 | ||
| - | We obtain this part from its iGEM kit plate location and transformed into our prepared BL21 (DE3) competent cells. A detailed gene cloning protocol can be found on this link. LINK</li> | + | We obtain this part from its iGEM kit plate location and transformed into our prepared BL21 (DE3) competent cells. A detailed gene cloning protocol can be found on this link. LINK</li></div> |
<div style="text-indent:35px">- FOR CONSTRUCTING: PART BBA_J23101 + BBA_E0240 | <div style="text-indent:35px">- FOR CONSTRUCTING: PART BBA_J23101 + BBA_E0240 | ||
| - | These parts are collected from iGEM kit plates also and the same cloning protocol LINK is performed afterwards. Successfully cloned parts are ligated according to this protocol. LINK</li> | + | These parts are collected from iGEM kit plates also and the same cloning protocol LINK is performed afterwards. Successfully cloned parts are ligated according to this protocol. LINK</li></div> |
<div style="text-indent:35px">- FOR CONSTRUCTING: BBA_J23115 + BBA_E0240 | <div style="text-indent:35px">- FOR CONSTRUCTING: BBA_J23115 + BBA_E0240 | ||
<li>These parts are also collected from iGEM kit plates and the same cloning protocol LINK is performed afterwards. Successfully cloned parts are ligated according to this protocol. LINK</li> | <li>These parts are also collected from iGEM kit plates and the same cloning protocol LINK is performed afterwards. Successfully cloned parts are ligated according to this protocol. LINK</li> | ||
After the cloning phases, the protein consumption of bacteria cultures is obtained and the protein concentrations are measured as follows: | After the cloning phases, the protein consumption of bacteria cultures is obtained and the protein concentrations are measured as follows: | ||
| - | </li> | + | </li></div> |
<div class="withImageCentered"> | <div class="withImageCentered"> | ||
<a href="http://placehold.it/600x600"><img src="https://static.igem.org/mediawiki/2014/thumb/6/67/ATOMS-Interlab_study1.png/800px-ATOMS-Interlab_study1.png"></a> | <a href="http://placehold.it/600x600"><img src="https://static.igem.org/mediawiki/2014/thumb/6/67/ATOMS-Interlab_study1.png/800px-ATOMS-Interlab_study1.png"></a> | ||
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<div class="navLR"> | <div class="navLR"> | ||
| - | <a class="navLinkLeft" href="https://2014.igem.org/Team:ATOMS-Turkiye/ | + | <a class="navLinkLeft" href="https://2014.igem.org/Team:ATOMS-Turkiye/Achievements">Achievements</a> |
| - | <a class="navLinkRight" href ="https://2014.igem.org/Team:ATOMS-Turkiye | + | <a class="navLinkRight" href ="http://parts.igem.org/cgi/partsdb/pgroup.cgi?pgroup=iGEM2014&group=ATOMS-Turkiye">Official Parts Page</a> |
| + | <a class="navLinkDoubleRight" href ="https://2014.igem.org/Team:ATOMS-Turkiye">Go to Home Page</a> | ||
</div> | </div> | ||
</div> | </div> | ||
Latest revision as of 03:57, 18 October 2014
Interlab-Study
- This year, our team was involved in the international scientific experiment study organized by iGEM and declared on the main page of the iGEM website. Considering the promising nature of intensifying international collaboration and its ability to obtain more significant and accurate results, we were delighted to take part in this study and organization.
- It is important to remind ourselves of the interlab measurement study basics and the expectations from each lab before explaining the kind of process we carried out and what we have accomplished by joining this study.
- As it is summarized on the iGEM Measurement Study page, participating team must fulfill these requirements:
1. Designing a wiki page about the contribution and the achievements of study.
2. Constructing the particular BioBricks defined clearly on the page.
(The results are shown below.)
3. Collecting fluorescence data from each of these parts.
(The results are sent to iGEM HQ and also shown below.)
4. Submitting these data through Interlab Study form.
(To check out our form: here )
a. Existing device: BBa_I20260 (J23101-B0032-E0040-B0015) in the pSB3K3 vector.
b. New device to be built by the iGEM team: BBa_J23101 + BBa_E0240 (B0032-E0040-B0015), must be built in the pSB1C3 backbone
c. New device to be built by the iGEM team: BBa_J23115 + BBa_E0240 (B0032-E0040-B0015), must be built in the pSB1C3 backbone
- PRE-EXPERIMENTAL PREPARATION:
We planned to use E.coli BL21 (DE3) strain in order to obtain high amounts of protein yield enabling us to calculate the fluorescence emission. Prior for the cloning process, we prepared competent cells using this protocol. LINK
- FOR CLONING: BBA_I20260
We obtain this part from its iGEM kit plate location and transformed into our prepared BL21 (DE3) competent cells. A detailed gene cloning protocol can be found on this link. LINK
- FOR CONSTRUCTING: PART BBA_J23101 + BBA_E0240
These parts are collected from iGEM kit plates also and the same cloning protocol LINK is performed afterwards. Successfully cloned parts are ligated according to this protocol. LINK
- FOR CONSTRUCTING: BBA_J23115 + BBA_E0240
These parts are also collected from iGEM kit plates and the same cloning protocol LINK is performed afterwards. Successfully cloned parts are ligated according to this protocol. LINK
After the cloning phases, the protein consumption of bacteria cultures is obtained and the protein concentrations are measured as follows:
