Team:Paris/Addressing testing

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<center> [[team:Paris/WetLab#WetLab| Main]] - [[Team:Paris/Addressing_testing#top|Addressing]] - [[Team:Paris/Production_testing#top| Production]] - [[Team:Paris/Transduction_testing#top | reception]] - </center>
<center> [[team:Paris/WetLab#WetLab| Main]] - [[Team:Paris/Addressing_testing#top|Addressing]] - [[Team:Paris/Production_testing#top| Production]] - [[Team:Paris/Transduction_testing#top | reception]] - </center>
<center> '''Addressing'''</center>
<center> '''Addressing'''</center>
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<font color=yellow>Ne vous prenez pas trop la tête avec la description des constructions. Il faut surtout faire des liens vers nos parts à la registry</font>
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== Adressing system ==
== Adressing system ==

Revision as of 15:34, 18 October 2009

iGEM > Paris > WetLab > Addressing

Contents

WetLab

Main - Addressing - Production - reception -
Addressing


Ne vous prenez pas trop la tête avec la description des constructions. Il faut surtout faire des liens vers nos parts à la registry

Adressing system

global constructions :


plasmid = PSB3T5


Time required : A lOT !!!!!



Experiments ran :

column 1 column 2 column 3 column 4
PCR :

ClyA Cterm matrix : ? Oligo : TM :

ClyA Nterm matrix : ? Oligo : TM :

mRFP Cterm matrix : ? Oligo : TM :

mRFP Nterm plasmid : ? Oligo : TM :

PCR :

-

PCR :

-

PCR :

-

Verification on gel :

ok

Verification on gel :

-

Verification on gel :

-

Verification on gel :

-

Purification on gel :

ok

Purification on gel :

-

Purification on gel :

-

Purification on gel :

-

digestion:

ClyA Cterm S/P

RFP Nterm X/P

PBAD vector : ? E/S


digestion:

ClyA Cter-RFP Nter vector PSB1A3 E/X

digestion:

-

digestion:

-

verification digestion:

ok

verification digestion:

ok

verification digestion:

-

verification digestion:

-


ligation:

ClyA Cter-RFP Nter vector PSB1A3

ligation:

PBAD E/S ClyA Cter-RFP Nter PSB1A3 E/X (x2) PBAD S/P ClyA Cter-RFP Nter PSB? X/P (x2)

ligation:

-

ligation:

-

PCR colo :

ok

PCR colo :

ok

PCR colo :

-

PCR colo :

-


miniprep:

clone :

miniprep:

clone :

miniprep:

-

miniprep:

-


sequencing :

ok

sequencing :

ok

sequencing :

-

sequencing :

-

stock glycerol:

S? S?

stock glycerol

S?

stock glycerol

-

stock glycerol

-



Functional Testing:

PBAD ClyA RFP was transformed into Top10 bacteria in order to localize the fluorescence, we are supposed to have a superior fluorescence in the membrane.


PBAD ClyA RFP on PSB3T5 was transformed into Delta Tol bacteria , in this case we are supposed to see fluorescent vesicles went the medium contains 1 % arabinose , and to have no fluorescent on 1% glucose.


Export system

We finally thought that it won't be neccesary to overexpress the Tat system, nevertheless we have run a few experiments before starting to focus on others parts of the project.


Time required : A week.



Experiments ran :

column 1 column 2 column 3 column 4


PCR :

TatABCE matrix :

PCR : PCR : PCR :
Verification on gel :

ok

Verification on gel :

-

Verification on gel :

-

Verification on gel :

-

Purification on gel :

ok

Purification on gel :

-

Purification on gel :

-

Purification on gel :

-


digestion:

TatABCE

digestion: digestion: digestion:
verification digestion:

ok

verification digestion:

-

verification digestion:

-

verification digestion:

-


ligation:

TatABCE

ligation: ligation: ligation:
PCR colo :

ok

PCR colo :

-

PCR colo :

-

PCR colo :

-

miniprep:

STOPPED

miniprep:

-

miniprep:

-

miniprep:

-

sequencing :

-

sequencing :

-

sequencing :

-

sequencing :

-


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