Difference between revisions of "Team:Czech Republic/Parts"

(Basic Part)
Line 22: Line 22:
 
* Pheromone receptor (C. albicans) - [http://parts.igem.org/Part:BBa_K1690004 BBa_K1690004]
 
* Pheromone receptor (C. albicans) - [http://parts.igem.org/Part:BBa_K1690004 BBa_K1690004]
 
* Pheromone receptor (C. parapsilosis) - [http://parts.igem.org/Part:BBa_K1690005 BBa_K1690005]
 
* Pheromone receptor (C. parapsilosis) - [http://parts.igem.org/Part:BBa_K1690005 BBa_K1690005]
 +
 +
The BioBricks above were constructed by Module 2, where you can find [https://2015.igem.org/Team:Czech_Republic/Project/Orthogonal_signals_and_receptors#Construction details of their construction and function].
  
 
Also, 3 different reporters ready to use in Saccharomyces were prepared and sent:
 
Also, 3 different reporters ready to use in Saccharomyces were prepared and sent:
Line 28: Line 30:
 
* pCYC1v3_GFP (Yeast reporter) - [http://parts.igem.org/Part:BBa_K1690007 BBa_K1690007]
 
* pCYC1v3_GFP (Yeast reporter) - [http://parts.igem.org/Part:BBa_K1690007 BBa_K1690007]
 
* pTv3_GFP (Yeast reporter) - [http://parts.igem.org/Part:BBa_K1690008 BBa_K1690008]
 
* pTv3_GFP (Yeast reporter) - [http://parts.igem.org/Part:BBa_K1690008 BBa_K1690008]
 +
 +
These BioBricks were constructed by Module 1, where you can find [https://2015.igem.org/Team:Czech_Republic/Project/Synthetic_haploids#Construction details of their construction and function].
  
 
= Part Collection =
 
= Part Collection =

Revision as of 12:41, 18 September 2015

Parts

Description

Read more...

Basic Part

Several Basic parts were constructed during the summer. We contributed to the Registry with 8 different basic parts, ready to use in Saccharomyces cerevisiae. Function of all these parts was experimentally validated.

We sent 4 different mating pheromones:

  • Mating pheromone (S. cerevisiae) - [http://parts.igem.org/Part:BBa_K1690000 BBa_K1690000]
  • Mating pheromone (C. albicans) - [http://parts.igem.org/Part:BBa_K1690001 BBa_K1690001]
  • Mating pheromone (C. tropicalis) - [http://parts.igem.org/Part:BBa_K1690002 BBa_K1690002]
  • Mating pheromone (L. elongisporus) - [http://parts.igem.org/Part:BBa_K1690003 BBa_K1690003]

And with the sequences of 2 different pheromone receptors:

  • Pheromone receptor (C. albicans) - [http://parts.igem.org/Part:BBa_K1690004 BBa_K1690004]
  • Pheromone receptor (C. parapsilosis) - [http://parts.igem.org/Part:BBa_K1690005 BBa_K1690005]

The BioBricks above were constructed by Module 2, where you can find details of their construction and function.

Also, 3 different reporters ready to use in Saccharomyces were prepared and sent:

  • pADH1_GFP (Yeast reporter) - [http://parts.igem.org/Part:BBa_K1690006 BBa_K1690006]
  • pCYC1v3_GFP (Yeast reporter) - [http://parts.igem.org/Part:BBa_K1690007 BBa_K1690007]
  • pTv3_GFP (Yeast reporter) - [http://parts.igem.org/Part:BBa_K1690008 BBa_K1690008]

These BioBricks were constructed by Module 1, where you can find details of their construction and function.

Part Collection

Our submitted parts can be divided into two separate collections:

Signals & Receptors

  • Mating pheromone (S. cerevisiae) - [http://parts.igem.org/Part:BBa_K1690000 BBa_K1690000]
  • Mating pheromone (C. albicans) - [http://parts.igem.org/Part:BBa_K1690001 BBa_K1690001]
  • Mating pheromone (C. tropicalis) - [http://parts.igem.org/Part:BBa_K1690002 BBa_K1690002]
  • Mating pheromone (L. elongisporus) - [http://parts.igem.org/Part:BBa_K1690003 BBa_K1690003]
  • Pheromone receptor (C. albicans) - [http://parts.igem.org/Part:BBa_K1690004 BBa_K1690004]
  • Pheromone receptor (C. parapsilosis) - [http://parts.igem.org/Part:BBa_K1690005 BBa_K1690005]

Yeast reporters

pADH1_GFP (Yeast reporter) - [http
//parts.igem.org/Part:BBa_K1690006 BBa_K1690006] : GFP under the control of constitutive pADH1 promoter
pCYC1v3_GFP (Yeast reporter) - [http
//parts.igem.org/Part:BBa_K1690007 BBa_K1690007] : GFP under the control of constitutive pCYC1v3 promoter
pTv3_GFP (Yeast reporter) - [http
//parts.igem.org/Part:BBa_K1690008 BBa_K1690008] : GFP under the control of repressible pTet promoter