Team:Mexico-UNAM-CINVESTAV/Notebook/Week One

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==''Monday''==
==''Monday''==
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==='''We discussed and concluded that the Igem’s vector  quantity  is not enough.'''===
 
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==='''First step:  Transform using only the vector to get enough material. '''===
 
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==='''We are going to  transform Psb1C3  from plate.  To do  this:'''===
 
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*''' We prepared  stock solutions of Cloramphenicol, Kanamicyn, Ampicilin.'''
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*''' We got plasmid PSB1C3 from the Biobrick plate. '''
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*''' 5 LB agar and 35ug/ml cloramphenicol plates made up . '''
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*''' We prepared stock solutions of Cloramphenicol, Kanamicyn, Ampicilin.'''
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*''' We completed the procedure to make quimio and electro-competent cells.'''
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*''' Some LB agar and 35ug/ml cloramphenicol plates made up . '''
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*''' We al ready made quimio and electro-competent cells for transformation and stored in aliquots in containers vials at -80 degrees..'''
==''Tuesday''==
==''Tuesday''==
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==='''Finished competent cells and stored in aliquots in containers vials at -80 degrees.'''===
 
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==='''We transformed DH5α cells with Psb1C3.'''===
 
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==='''We transformed DH5α cells with PSB1C3.'''===
==''Wednesday''==
==''Wednesday''==
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==='''We have not obtained  transformats cells.'''===
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'''We have not obtained  transformats cells.'''
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==='''We checked out the Cloramphenicol'''===
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==='''dose and attempt again the transformation using Psb1C3.'''===
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'''We checked out Cloramphenicol stock concentration and attempt again the transformation used PSB1C3.'''
==''Thursday''==
==''Thursday''==
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==='''The primers arrived '''===
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'''The primers arrived and we proceed to amplify the modules by PCR.'''
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==='''and we proceed to amplify the modules by PCR.'''===
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[[Image:PCR.gif]]
[[Image:PCR.gif]]
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==='''The amplification was ok and to quantify DNA concentrations'''===
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'''The amplification was ok and we had looking for a nano spectrophotometer.'''
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==='''we had looking for a nano spectrophotometer.'''===
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'''we made quantification of DNA concentrations'''

Latest revision as of 19:55, 27 October 2010



As summer project our experimental work began in August, after intensive brainstorming we finnaly decide

between two options.


*Inmunoresponse using Synthetic Biology.

*Cryobiology applied to plant crops.

After a selection process we chose the Cryobiology Project.

The final design of the expressions modules were as follow:

caption


Next Notebook sheet is our reference for primers and ligations and for modules Assembly:


Primers1.JPG

The AFP (Antifreeze Protein) was synthesized as follow:

Vector001.jpg

Week #1

06th September - 10th September 2010

Monday

  • We got plasmid PSB1C3 from the Biobrick plate.
  • We prepared stock solutions of Cloramphenicol, Kanamicyn, Ampicilin.
  • Some LB agar and 35ug/ml cloramphenicol plates made up .
  • We al ready made quimio and electro-competent cells for transformation and stored in aliquots in containers vials at -80 degrees..

Tuesday

We transformed DH5α cells with PSB1C3.

Wednesday

We have not obtained transformats cells.

We checked out Cloramphenicol stock concentration and attempt again the transformation used PSB1C3.

Thursday

The primers arrived and we proceed to amplify the modules by PCR.

PCR.gif

The amplification was ok and we had looking for a nano spectrophotometer.

we made quantification of DNA concentrations

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