Team:UC Chile/Bacto/Notepad

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Revision as of 17:39, 6 June 2012

Cyanolux & SpiderColi - Pontificia Universidad Católica de Chile, iGEM 2012

March

Week 1: 5-9 march

Tu:The whole team met for the first time after the vacations of february. We discussed our scheduling and divided ourselves in two groups: Cyano and Bactomythril. The leaders of each group were elected: Carla (Cyano) and Claudia (Bactomithril).

Cyano: Wetlab: Simon, Seba / Drylab: Carla, Tamara, Isaac

Biomithril: Wetlab: Ulises, Bryon / Drylab: Claudia, Emilia, Max

Carla and Max were chosen to maintain the wiki updated.

Bernardo and Rolando are going to collaborate with both groups.

Also, we scheduled meetings of the whole team every Friday or Tuesday (depending on the availability of the majority of the team), and meetings with the whole team and our advisor, Professor Rodrigo Gutierrez, every other Thursday. Likewise, each group should have their own meetings.

Finally, we decided to work based on delivery dates. Each member should compromise to complete a task in specific time intervals.

Week 2: 12-16 march

Week 3: 19-23 march

Week 4: 26-30 march

April

Week 1: 2-6 april

Week 2: 9-13 april

We: We have lunch-meeting where we decide to change our responsabilities.

Wetlab: Brion y Max

Modelation: Emilia y Ulises

Wiki: Claudia

Our task for next week are:

Wetlab: Work with the new material that arrived, primer and plasmid.

Modelation: Read paper Hayashi 1999, Hypotheses that correlate the sequence, structure, and mechanical properties of spider silk proteins. Learn how to use the software.

Week 3: 16-20 april

We: We have our regular lunch-meeting. Gibson Assembly of Working Plasmid Construct and transformation.

Th: Meeting with Rodrigo Gutierrez We have a colony after the transformation!!! :D

a) Removing the parts that deal to make the construct (Working Plasmid) and transforming them into Colis.

b) Miniprep of all constructs that transform and obtain DNA

c) Constructs were amplified in the thermocycler. We did PCR, but wasn’t in good condition, running buffer was weird was going very slow so we decided to leave it for next week.

Week 4: 23-27 april

Tu: Meeting with Rodrigo

We: We have a stand in Feria Ingenia

Th: We participate in a conversation table in Feria Ingenia. Livestream

a) PCR amplification of the constructs. Of the 7 constructs to amplify, we can only see 5 in gel electrophoresis. Is due in large part because one of them is 42kb (HIV cleavage site) and a 2 kb (vector backbone; psB1K3) and the gel was not as resolute (1%) to observe clearly.

b) The gel was run with the 2 constructs mentioned. This time, add more of them (4UL template in PCR) to ensure that they were present in our tubes.

c) We observed 2 bands for both constructs.

d) We made the decision to leave the Gibson for next week.

May

Week 1: 1-4 may

Week 2: 7-11 may

Week 3: 14-18 may

Week 4: 21-25 may

Week 5: 28 may-1 june

June

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@@ Line 78: / Line 78: @@
 '''Th:''' Meeting with Rodrigo Gutierrez
 We have a colony after the transformation!!! :D
+a) Removing the parts that deal to make the construct (Working Plasmid) and transforming them into Colis.
+b) Miniprep of all constructs that transform and obtain DNA
+c) Constructs were amplified in the thermocycler. We did PCR, but wasn’t in good condition, running buffer was weird was going very slow so we decided to leave it for next week.
@@ Line 87: / Line 93: @@
 '''Th:''' We participate in a conversation table in ''Feria Ingenia''. [http://twitcam.livestream.com/9pslw Livestream]
+a) PCR amplification of the constructs. Of the 7 constructs to amplify, we can only see 5 in gel electrophoresis. Is due in large part because one of them is 42kb (HIV cleavage site) and a 2 kb (vector backbone; psB1K3) and the gel was not as resolute (1%) to observe clearly.
+b) The gel was run with the 2 constructs mentioned. This time, add more of them (4UL template in PCR) to ensure that they were present in our tubes.
+c) We observed 2 bands for both constructs.
+d) We made the decision to leave the Gibson for next week.