Team:UTP-Panama/Week 16

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(Difference between revisions)
(Transformation of Competent Cells)
(Transformation of Competent Cells)
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Positive Control: 50µL competent cells + 2µL BBa_K410000 is resuspended.<br>
Positive Control: 50µL competent cells + 2µL BBa_K410000 is resuspended.<br>
Negative Control: 50µL competent cells  <br>
Negative Control: 50µL competent cells  <br>
 +
 +
1. In 3 eppendorf tubes was added the specified amount in positive control and were resuspended.<br>
 +
2. Tubes in previous step remained settled in ice during 30 minutes.<br>
 +
3. Afterwards, cold shock carried out, the 4 eppendorf are set in water bath for a minute. (T=42°C)<br>
 +
4. Right after the water bath, it remained in ice during 5 minutes.<br>
 +
5. Added 200µL cold SOC to each eppendorf tube, then resuspended<br>
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6. Every petri dish was sealed with parafilm and was appropriately labeled; afterwards they were put in the incubator<br>
==September 20==
==September 20==

Revision as of 22:15, 28 September 2011

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Week 16: September 19 to 24

September 19

WET LAB

I. DIGESTION

For each Eppendorf PCR was added the following:
1. 10µL DNA (residue of mini prep)
2. 32.5 µL water ultra-pure distilled water
3. 5µL buffer (P2)
4. 0.5µL BSA
5. 1µL enzyme 1 (EcoRI)
6. 1µL enzyme 2 (Spel)
____________
Total 50µL

19sep dig.jpg

There was added the 6 components to the small tube of PCR.
Note: Make sure to mix all the components in the centrifuge

7. Two (2)eppendorf tubes were incubated in the thermocycler during 1 hour at 37°C :
a. UPSTREAM (GaTech)
b. DOWNSTREAM (Bristol)
8. Once again, tubes were incubated in the thermocycler during 20 minutes at 80°C
9. We stored at -20°C until it is used for ligation.

Transformation of Competent Cells

A. 4 petri dishes were filled with 5mL of solid LB 3 positive controls and 1 negative control. Calculo 19sept.jpg

Total: 19.36µL para 20µL de LB

'Content of controls:'
Positive Control: 50µL competent cells + 2µL BBa_K410000 is resuspended.
Negative Control: 50µL competent cells

1. In 3 eppendorf tubes was added the specified amount in positive control and were resuspended.
2. Tubes in previous step remained settled in ice during 30 minutes.
3. Afterwards, cold shock carried out, the 4 eppendorf are set in water bath for a minute. (T=42°C)
4. Right after the water bath, it remained in ice during 5 minutes.
5. Added 200µL cold SOC to each eppendorf tube, then resuspended
6. Every petri dish was sealed with parafilm and was appropriately labeled; afterwards they were put in the incubator

September 20

Scientific Comunication Activities

Tree sessions:
Session 1: Civil Engineering Faculty (morning) Session 2: Electrical Engineering Faculty (afternoon) Session 3: Civil Engineering Faculty (afternoon) Presentation (by the students of iGEM UTP-Panama) about the following topics:
What's SynBio?
Applications of SynBio
What's iGEM?
What are we doing? (our project)
Future projects

WET LAB

(Objetives or Title): --ESCRIBIR Y MEJORAR LAB--

September 21

WET LAB

(Objetives or Title): --ESCRIBIR Y MEJORAR LAB--

September 22

WET LAB

(Objetives or Title): --ESCRIBIR Y MEJORAR LAB--

September 23

WET LAB

(Objetives or Title): --ESCRIBIR Y MEJORAR LAB-- DNA Device Submission: Explicar

September 24

GENERAL SESSION

Afternoon: Talikng about WET LAB final activities. Design of the "SB UTP 1.0" and "SB UTP Project 1.0" Discussion about remake the experiments with the Bristol and Gatech Biobricks (experience).

September 25

WET LAB

Sunday extra experiments session