Team:UTP-Panama/Week 9

WEEK 9: AUGUST 1 to 6

August 1

WET LAB

First Wet lab visit of the UTP Panama iGEM Team.
Work Session #27
Place INDICASAT
Advisor at INDICASAT: Ricardo Correa
In this day the students know all the Lab instalation, and some of the basics instruments and rules of the lab.

Work Session #27 (afternoon) Project Design and Modeling
All the team discuss the final Biobrick of our team. In this sense we select to modify and improve the Bristol 2010 Project, the Gatech 2010 Project and the UNAM-Cinvestav 2010 project. We establish the Human Practice project activities schedule.

August 2

Project Discussion & Outlines

Place INDICASAT
Work Session #28 (morning)
Preliminar Project Design of our Project with the help of our Instructor Grimaldo E. Ureña and and our advisors Zeus Capitan and Ricardo Correa, based on the selected Biobricks of the August 1 meetings and conversatory. The Wet Lab advisors establish a schedule of activities to accomplish for the students. The students organizated all the supplies and reagents to the projects first stages.

August 3

WET LAB

Place: INDICASAT (Morning)
Preparation of Buffers, organize supplies and reagents. Advisors: Ricardo, Grimaldo Elías y Lucía.

Work Session #30 (afternoon)
General Meeting, about the porject

August 4

WET LAB

Place: INDICASAT (morning)
Work Session 31
Preparation of Buffers, reagents etc, to create Competent Cells.
--WRITE HERE THE PROTOCOL--. Tomorrow we must see what happen it. Advisor: Ricardo Correa & Grimaldo Ureña.

HUMAN PRACTICE & PROJECT DESIGN

Work Session 32 (afternoon) a). Meeting about final propousal of Human Practice Project. b). Discussion about betters ways of develop our project.

August 5

Work session #33(morning)
Preparation of more reagents for make Competents Cells. Work Session #34 (afternoon)
Discussion of Huma Practice project. We propouse some diferents projects as develop of a model or program to better scientific comunication of SynBio.

OBJECTIVE: Prepare buffer for Dirty Mini Prep (separation of plasmid DNA of the chromosome). 1. To prepare: Buffer P1 (kept at 4 º C) (500mL) • Tris-HCl pH 8.0 50 mM • 10 mM EDTA • RNAse A 100 mg / mL (cold) Buffer P2 (500 ml) • 200mm NaOH • SDS (1%) Buffer P3 (500 ml) • 3M potassium acetate pH5.5

2. After preparing the buffer pH were regulated to get what was needed. 3. We filter the buffer.

5/8/2011 OBJECTIVE: Preparation of culture media. 1. Prepare culture media for the growth of competent cells. 2. Heat the solid LB. 3. Prepare 50mg/ml Ampicillin stock solution

Amp 6.25g sólido/10mL More antibiotic to 10mL water and then filtered. 4. We use a portion of the agar. 5. To this we add a volume agar ampicillin with a lower concentration, so from our stock solution:

C1V1 = c2v2

 = V1

V1 = 0.02mL

6. The previous amount was changed as insufficient. Finally added to the plates 80 of ampicillin solution. 7. These dishes were left ready for the next experience.

August 6

General Session

Work Session #35 (morning) Project Design, Conversatory about ways to implementate a model for our project.