Team:Sevilla/Week4

From 2011.igem.org

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<img style="z-index:-5;margin-top:-51px;margin-left:155px;" src="https://static.igem.org/mediawiki/2011/f/f8/Web.png" />
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$("#par2 a:last").css("text-decoration","underline");
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$("#fridayProtocols").hide();
$("#fridayProtocols").hide();
$("#weekendProtocols").hide();  
$("#weekendProtocols").hide();  
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$(".SW").button();
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$("#mondayBP").button();
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$("#tuesdayBP").button();
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$("#wednesdayBP").button();
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$("#thursdayBP").button();
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font-size: 12px ! important;
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<p>
<p>
-
The primers we ordered last week should have come today, but as usual, they haven't (bureaucracy, lazy postmen, maybe a natural catastrophe...). This means we cannot do much today, except for planning our next steps, searching for more information about how to build logic gates or deciphering the intrincate registry of parts. We've realised we have some useful biobricks in our distribution kit we didn't even know about.
+
The primers we ordered last week should have come today, but as usual, they haven't (bureaucracy, lazy postmen, maybe a natural catastrophe...). This means we can't do much today, except plan our next steps and search for more information about how to build logic gates, or decipher the intrincate registry of parts. We've realised we have some useful biobricks in our distribution kit which we didn't even know about.
</p>
</p>
-
<p>Another useful thing to spend time: preparing the videos for the people who gave us money through the crowdfunding platform, in appreciation for their donations.
+
 
 +
<p>Another useful way of spending time: preparing the videos for the people who gave us money through the crowdfunding platform, in appreciation for their donations.
</p>
</p>
<p>
<p>
-
Even more useful: piling the pipette's tips to build a giant ring!
+
Even more useful: joining together pipette tips to build a giant ring!
</p>
</p>
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</div>
</div>
-
<p>In. Mid vel vel elementum, placerat tincidunt, vut lacus purus nunc massa a habitasse? Ac pid elementum aliquam, natoque! Porttitor facilisis amet lacus, ridiculus nascetur! Sociis vel aenean natoque penatibus aliquam in, augue mauris, dictumst, nunc mid platea a! Massa? Vut dis purus. Odio magna nec. Lorem ut turpis adipiscing scelerisque dis, scelerisque. Sed quis, porttitor et pulvinar in. Massa sit, porta urna nunc auctor non elementum! Augue dolor cum sociis, dignissim elementum. Integer. Penatibus. Phasellus et porta nec! Hac in nec porttitor ridiculus rhoncus. Hac natoque mid est nunc platea nisi sed habitasse! Amet nec placerat ultricies egestas.
+
<p>
-
 
+
-
Vel cum diam, lorem integer et montes, nec placerat, turpis lacus nec placerat, rhoncus rhoncus, a porta augue ac! Et aliquet. Porttitor diam egestas, non vut etiam montes, aliquet? Pellentesque. Dolor nascetur amet. Adipiscing sed pulvinar cursus! Urna in, in turpis duis in sit placerat, vut non aliquam? Mattis habitasse augue mus. Pulvinar auctor natoque est lacus porta sagittis! A in massa lundium? In non, lundium nisi magna proin elementum sed porttitor sed amet risus a aliquet mid a? Proin turpis, ac magna, dictumst lorem tincidunt penatibus sociis rhoncus? Duis cursus sit diam amet nisi mattis egestas habitasse diam.
+
</p>
</p>
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<p>
<p>
-
Our primers still don't arrive, but to ease our boredom, the university's cabling decides to short-circuit! Our incubator starts steaming, the fire alarm starts ringing, the fridges don't work, our frozen cultures start to melt, but we don't panic...until we find out the Internet doesn't work either!!!
+
Our primers still haven't arrived, but happily, to ease our boredom the university's cabling
-
 
+
decides to short-circuit! Our incubator starts steaming, the fire alarm starts ringing, the fridges
 +
don't work, our frozen cultures start to melt, but we don't panic...until we find out the Internet
 +
doesn't work either!!!
</p>
</p>
-
 
<img src="https://lh6.googleusercontent.com/-_W5Zw0MToVQ/TjkvzOGMWCI/AAAAAAAAAgI/qEJHcFeSt2Y/s288/IMG_5117.JPG" style=padding-left:160px;"height="192" width="288" />
<img src="https://lh6.googleusercontent.com/-_W5Zw0MToVQ/TjkvzOGMWCI/AAAAAAAAAgI/qEJHcFeSt2Y/s288/IMG_5117.JPG" style=padding-left:160px;"height="192" width="288" />
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</br>
</br>
</div>
</div>
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<p>In. Mid vel vel elementum, placerat tincidunt, vut lacus purus nunc massa a habitasse? Ac pid elementum aliquam, natoque! Porttitor facilisis amet lacus, ridiculus nascetur! Sociis vel aenean natoque penatibus aliquam in, augue mauris, dictumst, nunc mid platea a! Massa? Vut dis purus. Odio magna nec. Lorem ut turpis adipiscing scelerisque dis, scelerisque. Sed quis, porttitor et pulvinar in. Massa sit, porta urna nunc auctor non elementum! Augue dolor cum sociis, dignissim elementum. Integer. Penatibus. Phasellus et porta nec! Hac in nec porttitor ridiculus rhoncus. Hac natoque mid est nunc platea nisi sed habitasse! Amet nec placerat ultricies egestas.
+
<p>
-
 
+
-
Vel cum diam, lorem integer et montes, nec placerat, turpis lacus nec placerat, rhoncus rhoncus, a porta augue ac! Et aliquet. Porttitor diam egestas, non vut etiam montes, aliquet? Pellentesque. Dolor nascetur amet. Adipiscing sed pulvinar cursus! Urna in, in turpis duis in sit placerat, vut non aliquam? Mattis habitasse augue mus. Pulvinar auctor natoque est lacus porta sagittis! A in massa lundium? In non, lundium nisi magna proin elementum sed porttitor sed amet risus a aliquet mid a? Proin turpis, ac magna, dictumst lorem tincidunt penatibus sociis rhoncus? Duis cursus sit diam amet nisi mattis egestas habitasse diam.
+
</p>
</p>
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<p>
<p>
-
 
+
More mini-preps, more transformations, and more competent cells to kill the time while the
-
More mini-preps, transformations, competent cells to kill the time while the primers arrive, but at least we're improving and the results are pretty good! Besides, we're trying a new protocol to purify DNA after digestions. Tomorrow we'll see how it goes.
+
primers arrive, but at least we're improving and the results are pretty good! Besides, we're
-
 
+
trying out a new protocol to purify DNA after digestions. Tomorrow we'll see how it goes.
</p>
</p>
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</br>
</br>
</div>
</div>
-
<p>In. Mid vel vel elementum, placerat tincidunt, vut lacus purus nunc massa a habitasse? Ac pid elementum aliquam, natoque! Porttitor facilisis amet lacus, ridiculus nascetur! Sociis vel aenean natoque penatibus aliquam in, augue mauris, dictumst, nunc mid platea a! Massa? Vut dis purus. Odio magna nec. Lorem ut turpis adipiscing scelerisque dis, scelerisque. Sed quis, porttitor et pulvinar in. Massa sit, porta urna nunc auctor non elementum! Augue dolor cum sociis, dignissim elementum. Integer. Penatibus. Phasellus et porta nec! Hac in nec porttitor ridiculus rhoncus. Hac natoque mid est nunc platea nisi sed habitasse! Amet nec placerat ultricies egestas.
+
<p><p><strong>Ethanol Purification</strong></p>
 +
<p>-MATERIALS</p>
 +
<p>
 +
1. Absolute Ethanol  (100%) at -20ºC.
 +
</p>
 +
<p>
 +
2. Ethanol  95%  at  -20ºC.
 +
</p>
 +
<p>
 +
3. Temperature regulated centrifuge.
 +
</p>
 +
<p>
 +
4. Feezer at -80ºC.
 +
</p>
 +
<p>
 +
5. Milli-Q water
 +
</p>
 +
<p>
 +
6. Sodium Acetate 3M.
 +
</p>
 +
<p>
 +
7. Ice.
 +
</p>
-
Vel cum diam, lorem integer et montes, nec placerat, turpis lacus nec placerat, rhoncus rhoncus, a porta augue ac! Et aliquet. Porttitor diam egestas, non vut etiam montes, aliquet? Pellentesque. Dolor nascetur amet. Adipiscing sed pulvinar cursus! Urna in, in turpis duis in sit placerat, vut non aliquam? Mattis habitasse augue mus. Pulvinar auctor natoque est lacus porta sagittis! A in massa lundium? In non, lundium nisi magna proin elementum sed porttitor sed amet risus a aliquet mid a? Proin turpis, ac magna, dictumst lorem tincidunt penatibus sociis rhoncus? Duis cursus sit diam amet nisi mattis egestas habitasse diam.
+
<p>
 +
PROTOCOL
 +
</p>
 +
<p>
 +
1. Add 2 volumes of very cold absolute etanol (preserved at -20ºC) to the sample (the sample must have 30μL, so you must add  60μL of ethanol). Hacer este paso y el siguiente en hielo.
 +
</p>
 +
<p>
 +
2. Add  10μL of Sodium Acetate (only if the sample´s colume is  90μL,as it must be).
 +
</p>
 +
<p>
 +
3. Incubate for 1h a -80ºC (it can be more time if the DNA fragments are very little). It can also be an overnight incubation).
 +
</p>
 +
<p>
 +
4. Centrifugate for 30 minutes at 0ºC at  máximum speed (>10000g).
 +
</p>
 +
<p>
 +
5. Discart  70μL of supernatant. You may use a pipette without touching the eppendorf bottom.
 +
</p>
 +
<p>
 +
6. Add  800μL of cold etanol 95% and invert the tubes once or twice inmediately. After that, incubate for  1 h at -80ºC.
 +
</p>
 +
<p>
 +
7. Centrifugate at 4ºC for 10 minutes at máximum speed(>10000g).
 +
</p>
 +
<p>
 +
8. Discart  770μL of supernatant. You may use a pipette without touching the eppendorf bottom.
 +
</p>
 +
<p>
 +
9. Let the pellet dry. (It´s very important that the pellet is completely dry)You can use the stove at 37ºC.
 +
</p>
 +
<p>
 +
10. Add  10μL  of Milli-Q wáter to the sample.
 +
<p>
 +
 
 +
 
 +
 
 +
</p>
</p>
</p>
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<p>
<p>
-
After purifications we run an electrophoresis and it turns out to be so beautiful we almost cry! Everything has gone as expected, the digestions are ok, but the NanoDrop results say we've lost too much DNA in the process. </p>
+
After purifications we run an electrophoresis and it turns out so beautifully we almost
-
 
+
cry! Everything has gone as expected, the digestions are ok, but the NanoDrop results
 +
say we've lost too much DNA in the process.</p>
<p>
<p>
-
The primers are here at last! We can start with the pcr reactions to regenerate plasmid backbones and obtain some genes from our donated strains.Let's see how we go...
+
The primers are here at last! We can finally begin the PCR reactions to regenerate
 +
plasmid backbones and obtain some genes from our donated strains. Let's see how we
 +
go...
 +
 
</p>
</p>
 +
<img src="https://lh3.googleusercontent.com/-2IlQLrH-_E8/Tju2g0_kTtI/AAAAAAAAAmk/_K-tv6TOEF8/s288/IMG_5204.JPG" style=padding-left:200px;"height="192" width="288" />
<img src="https://lh3.googleusercontent.com/-2IlQLrH-_E8/Tju2g0_kTtI/AAAAAAAAAmk/_K-tv6TOEF8/s288/IMG_5204.JPG" style=padding-left:200px;"height="192" width="288" />
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</br>
</br>
</div>
</div>
-
<p>In. Mid vel vel elementum, placerat tincidunt, vut lacus purus nunc massa a habitasse? Ac pid elementum aliquam, natoque! Porttitor facilisis amet lacus, ridiculus nascetur! Sociis vel aenean natoque penatibus aliquam in, augue mauris, dictumst, nunc mid platea a! Massa? Vut dis purus. Odio magna nec. Lorem ut turpis adipiscing scelerisque dis, scelerisque. Sed quis, porttitor et pulvinar in. Massa sit, porta urna nunc auctor non elementum! Augue dolor cum sociis, dignissim elementum. Integer. Penatibus. Phasellus et porta nec! Hac in nec porttitor ridiculus rhoncus. Hac natoque mid est nunc platea nisi sed habitasse! Amet nec placerat ultricies egestas.
+
<p> <strong>PCR PROTOCOL</strong></p>
-
 
+
<p>We use the Maxime Premix kit to do our PCR. Maxime PCR PreMix contains:</p>
-
Vel cum diam, lorem integer et montes, nec placerat, turpis lacus nec placerat, rhoncus rhoncus, a porta augue ac! Et aliquet. Porttitor diam egestas, non vut etiam montes, aliquet? Pellentesque. Dolor nascetur amet. Adipiscing sed pulvinar cursus! Urna in, in turpis duis in sit placerat, vut non aliquam? Mattis habitasse augue mus. Pulvinar auctor natoque est lacus porta sagittis! A in massa lundium? In non, lundium nisi magna proin elementum sed porttitor sed amet risus a aliquet mid a? Proin turpis, ac magna, dictumst lorem tincidunt penatibus sociis rhoncus? Duis cursus sit diam amet nisi mattis egestas habitasse diam.
+
<p>
-
 
+
- i-MAX (II)DNA Polymerase.</p>
 +
<p>
 +
- dNTPs.</p>
 +
<p>
 +
- Reaction Buffer
</p>
</p>
 +
<p>
 +
- Gel Loading buffer.</p>
 +
<p> We only have to add 17 μL, 1 μL of DNA sample and 1 μL of each primers (Foward and Reverse)to the premix.<p>
 +
<p> PCR cicle
 +
</p>
 +
<p>
 +
1. 94ºC for 3 minutes.</p>
 +
<p>
 +
2. 94ºC for 30 seconds.</p>
 +
<p>
 +
3. 55ºC for 30 seconds.</p>
 +
<p>
 +
4. 72ºC for 3 minutes.</p>
 +
</p>.
 +
<p>Steps 2 to 4 must be repeated for 30 times</p>
 +
</div>
</div>
</div>
</div>
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<p>
<p>
-
Roberto has brought m&m's, lots of them!!!This is the best day of our lives.
+
Roberto has brought M&M's: lots of them!!!This is the best day of our lives. Besides, the PCR
-
</p>
+
results are really quite good, except for the fact that we've amplified the wrong BioBrick - it
 +
seems working here for so many hours has overheated our brains. We'll have to try again next
 +
week, and make sure we pay more attention.
-
<input type="button" value="Show Friday protocols" id="fridayBP">
+
</p>
-
</div>
 
-
 
-
 
-
<div id="fridayProtocols">
 
-
 
-
<div class="day">
 
-
</br>
 
-
<p>Friday Protocols</p>
 
-
</br>
 
-
</div>
 
-
<p>In. Mid vel vel elementum, placerat tincidunt, vut lacus purus nunc massa a habitasse? Ac pid elementum aliquam, natoque! Porttitor facilisis amet lacus, ridiculus nascetur! Sociis vel aenean natoque penatibus aliquam in, augue mauris, dictumst, nunc mid platea a! Massa? Vut dis purus. Odio magna nec. Lorem ut turpis adipiscing scelerisque dis, scelerisque. Sed quis, porttitor et pulvinar in. Massa sit, porta urna nunc auctor non elementum! Augue dolor cum sociis, dignissim elementum. Integer. Penatibus. Phasellus et porta nec! Hac in nec porttitor ridiculus rhoncus. Hac natoque mid est nunc platea nisi sed habitasse! Amet nec placerat ultricies egestas.
 
-
 
-
Vel cum diam, lorem integer et montes, nec placerat, turpis lacus nec placerat, rhoncus rhoncus, a porta augue ac! Et aliquet. Porttitor diam egestas, non vut etiam montes, aliquet? Pellentesque. Dolor nascetur amet. Adipiscing sed pulvinar cursus! Urna in, in turpis duis in sit placerat, vut non aliquam? Mattis habitasse augue mus. Pulvinar auctor natoque est lacus porta sagittis! A in massa lundium? In non, lundium nisi magna proin elementum sed porttitor sed amet risus a aliquet mid a? Proin turpis, ac magna, dictumst lorem tincidunt penatibus sociis rhoncus? Duis cursus sit diam amet nisi mattis egestas habitasse diam.
 
-
 
-
</p>
 
-
</div>
 
</div>
</div>
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<div class="summary">
<div class="summary">
-
<p>wwwwwwwwwwwwwwwwRhoncus nisi adipiscing, rhoncus. Porttitor urna rhoncus? A placerat scelerisque mattis lectus tristique magna pellentesque ac ac, et? Adipiscing penatibus porta. Turpis ultrices lorem vel vel massa elementum! Lorem vel lectus et integer porttitor magna aenean, quis magnis turpis aliquam? Sed enim? Placerat velit sit turpis penatibus enim. Enim cursus hac massa eu a cum etiam? Amet pid porta non tincidunt cum pellentesque eu a pid nisi ultrices? Lectus augue dictumst purus, velit scelerisque vut. A porttitor turpis, natoque aliquam elementum. Tristique, mauris turpis? Arcu tristique sed massa est nunc purus pellentesque, risus nec rhoncus, scelerisque ac urna porttitor, sit.
+
<p>We have a bit of a do to celebrate Roberto's birthday. Look how elegant we can be on special occasions!
</p>
</p>
-
<input type="button" value="Show weekend protocols" id="weekendBP">
+
<img src="https://lh5.googleusercontent.com/-hPzzVSFmuX4/Tj-sSlBbAqI/AAAAAAAAAvM/wSJLBnTY3jE/s400/IMG_5332.JPG" style=padding-left:200px;"height="267" width="400" />
 +
<p>We also spend the whole Sunday watching a "Game of Thrones" marathon at Marta's while eating pizza. What an awsome series! Highly recommended by Arcanum - you can't miss it!</p>
</div>
</div>
-
 
-
 
-
<div id="weekendProtocols">
 
-
<div class="day">
 
-
</br>
 
-
<p>Weekend Protocols</p>
 
-
</br>
 
-
</div>
 
-
<p>In. Mid vel vel elementum, placerat tincidunt, vut lacus purus nunc massa a habitasse? Ac pid elementum aliquam, natoque! Porttitor facilisis amet lacus, ridiculus nascetur! Sociis vel aenean natoque penatibus aliquam in, augue mauris, dictumst, nunc mid platea a! Massa? Vut dis purus. Odio magna nec. Lorem ut turpis adipiscing scelerisque dis, scelerisque. Sed quis, porttitor et pulvinar in. Massa sit, porta urna nunc auctor non elementum! Augue dolor cum sociis, dignissim elementum. Integer. Penatibus. Phasellus et porta nec! Hac in nec porttitor ridiculus rhoncus. Hac natoque mid est nunc platea nisi sed habitasse! Amet nec placerat ultricies egestas.
 
-
 
-
Vel cum diam, lorem integer et montes, nec placerat, turpis lacus nec placerat, rhoncus rhoncus, a porta augue ac! Et aliquet. Porttitor diam egestas, non vut etiam montes, aliquet? Pellentesque. Dolor nascetur amet. Adipiscing sed pulvinar cursus! Urna in, in turpis duis in sit placerat, vut non aliquam? Mattis habitasse augue mus. Pulvinar auctor natoque est lacus porta sagittis! A in massa lundium? In non, lundium nisi magna proin elementum sed porttitor sed amet risus a aliquet mid a? Proin turpis, ac magna, dictumst lorem tincidunt penatibus sociis rhoncus? Duis cursus sit diam amet nisi mattis egestas habitasse diam.
 
-
 
-
</p>
 
-
</div>
 
-
</div>
 
-
 
-
<input type="button" value="Show Week" class="SW" style="margin-bottom: 10px;z-index:4;">
 
</html>
</html>

Latest revision as of 22:28, 21 September 2011


Monday 1 August


The primers we ordered last week should have come today, but as usual, they haven't (bureaucracy, lazy postmen, maybe a natural catastrophe...). This means we can't do much today, except plan our next steps and search for more information about how to build logic gates, or decipher the intrincate registry of parts. We've realised we have some useful biobricks in our distribution kit which we didn't even know about.

Another useful way of spending time: preparing the videos for the people who gave us money through the crowdfunding platform, in appreciation for their donations.

Even more useful: joining together pipette tips to build a giant ring!


Monday Protocols



Tuesday 2 August


Our primers still haven't arrived, but happily, to ease our boredom the university's cabling decides to short-circuit! Our incubator starts steaming, the fire alarm starts ringing, the fridges don't work, our frozen cultures start to melt, but we don't panic...until we find out the Internet doesn't work either!!!


Tuesday Protocols



Wednesday 3 August


More mini-preps, more transformations, and more competent cells to kill the time while the primers arrive, but at least we're improving and the results are pretty good! Besides, we're trying out a new protocol to purify DNA after digestions. Tomorrow we'll see how it goes.


Wednesday Protocols


Ethanol Purification

-MATERIALS

1. Absolute Ethanol (100%) at -20ºC.

2. Ethanol 95% at -20ºC.

3. Temperature regulated centrifuge.

4. Feezer at -80ºC.

5. Milli-Q water

6. Sodium Acetate 3M.

7. Ice.

PROTOCOL

1. Add 2 volumes of very cold absolute etanol (preserved at -20ºC) to the sample (the sample must have 30μL, so you must add 60μL of ethanol). Hacer este paso y el siguiente en hielo.

2. Add 10μL of Sodium Acetate (only if the sample´s colume is 90μL,as it must be).

3. Incubate for 1h a -80ºC (it can be more time if the DNA fragments are very little). It can also be an overnight incubation).

4. Centrifugate for 30 minutes at 0ºC at máximum speed (>10000g).

5. Discart 70μL of supernatant. You may use a pipette without touching the eppendorf bottom.

6. Add 800μL of cold etanol 95% and invert the tubes once or twice inmediately. After that, incubate for 1 h at -80ºC.

7. Centrifugate at 4ºC for 10 minutes at máximum speed(>10000g).

8. Discart 770μL of supernatant. You may use a pipette without touching the eppendorf bottom.

9. Let the pellet dry. (It´s very important that the pellet is completely dry)You can use the stove at 37ºC.

10. Add 10μL of Milli-Q wáter to the sample.


Thursday 4 August


After purifications we run an electrophoresis and it turns out so beautifully we almost cry! Everything has gone as expected, the digestions are ok, but the NanoDrop results say we've lost too much DNA in the process.

The primers are here at last! We can finally begin the PCR reactions to regenerate plasmid backbones and obtain some genes from our donated strains. Let's see how we go...


Thursday Protocols


PCR PROTOCOL

We use the Maxime Premix kit to do our PCR. Maxime PCR PreMix contains:

- i-MAX (II)DNA Polymerase.

- dNTPs.

- Reaction Buffer

- Gel Loading buffer.

We only have to add 17 μL, 1 μL of DNA sample and 1 μL of each primers (Foward and Reverse)to the premix.

PCR cicle

1. 94ºC for 3 minutes.

2. 94ºC for 30 seconds.

3. 55ºC for 30 seconds.

4. 72ºC for 3 minutes.

.

Steps 2 to 4 must be repeated for 30 times


Friday 5 August


Roberto has brought M&M's: lots of them!!!This is the best day of our lives. Besides, the PCR results are really quite good, except for the fact that we've amplified the wrong BioBrick - it seems working here for so many hours has overheated our brains. We'll have to try again next week, and make sure we pay more attention.


Weekend


We have a bit of a do to celebrate Roberto's birthday. Look how elegant we can be on special occasions!

We also spend the whole Sunday watching a "Game of Thrones" marathon at Marta's while eating pizza. What an awsome series! Highly recommended by Arcanum - you can't miss it!

Retrieved from "http://2011.igem.org/Team:Sevilla/Week4"