Team:ETH Zurich/Data Page

From 2013.igem.org

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<h1>Our Favorite New Parts</h1>
<h1>Our Favorite New Parts</h1>
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<p align= "justify">   
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[http://parts.igem.org/Part:BBa_K1216002 Main Page] - Acetyl esterase (AES), BBa_K1216002 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert 5-Bromo-6-Chloro-3-indoxyl butyrate into an indigo analog precipitate <br>
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1. [http://parts.igem.org/Part:BBa_K1216002 Main Page] - Acetyl esterase (AES), BBa_K1216002 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert 5-Bromo-6-Chloro-3-indoxyl butyrate into an indigo analog precipitate <br>
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[http://parts.igem.org/Part:BBa_K1216005 MainPage] - Alkaline phosphatase with His tag and TEV cleavage site (phoA), BBa_K1216002 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert 5-Bromo-6-Chloro-3-indoxyl butyrate into an indigo analog precipitate <br>
+
2. [http://parts.igem.org/Part:BBa_K1216005 MainPage] - Alkaline phosphatase with His tag and TEV cleavage site (phoA), BBa_K1216002 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert 5-Bromo-6-Chloro-3-indoxyl butyrate into an indigo analog precipitate <br>
-
[http://parts.igem.org/Part:BBa_K1216007 MainPage] - pLuxR1 mutated promoter, BBa_K1216007 : the promoter has an EC<sub>50</sub> of 6.462 nM in liquid culture and 17'814nM on agar plates. This sensitivity is shifted 300'000 fold compared to the original BBa_R0062 pLuxR</p>
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3. [http://parts.igem.org/Part:BBa_K1216007 MainPage] - pLuxR1 mutated promoter, BBa_K1216007 : the promoter has an EC<sub>50</sub> of 6.462 nM in liquid culture and 17'814nM on agar plates. This sensitivity is shifted 300'000 fold compared to the original BBa_R0062 pLuxR</p>
<h1>Characterized Pre-existing Parts :</h1>
<h1>Characterized Pre-existing Parts :</h1>
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1. [http://parts.igem.org/Part:BBa_R0062:Experience Experience] - pLuxR wild type, BBa_R0062 : phoA gene from <i>Citrobacter</i>. We did Michealis-Menten kinetics of the phoA enzyme and also showed the conversion of PNP (para-nitrophenol phosphate) in a yellow analog precipitate.]<br>
1. [http://parts.igem.org/Part:BBa_R0062:Experience Experience] - pLuxR wild type, BBa_R0062 : phoA gene from <i>Citrobacter</i>. We did Michealis-Menten kinetics of the phoA enzyme and also showed the conversion of PNP (para-nitrophenol phosphate) in a yellow analog precipitate.]<br>
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2.[http://parts.igem.org/Part:BBa_J61032:Experience Experience] - Alkaline phosphatase, BBa_J61032 : phoA gene originated from <i>Citrobacter</i>. We did Michealis-Menten kinetics of the phoA enzyme and also showed the conversion of PNP (para-nitrophenol phosphate) in a yellow analog precipitate</p>
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2. [http://parts.igem.org/Part:BBa_J61032:Experience Experience] - Alkaline phosphatase, BBa_J61032 : phoA gene originated from <i>Citrobacter</i>. We did Michealis-Menten kinetics of the phoA enzyme and also showed the conversion of PNP (para-nitrophenol phosphate) in a yellow analog precipitate</p>
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<p align= "justify">  
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[http://parts.igem.org/Part:BBa_K1216000 MainPage] - β-Glucuronidase (gusA), BBa_K1216000 :We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert ______ into an red analog precipitate.<br>
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1. [http://parts.igem.org/Part:BBa_K1216000 MainPage] - β-Glucuronidase (gusA), BBa_K1216000 :We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert ______ into an red analog precipitate.<br>
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[http://parts.igem.org/Part:BBa_K1216003 MainPage] - β-N-Acetylglucosaminidase (nagZ), BBa_K1216003 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert ______ into an red analog precipitate.<br>
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2. [http://parts.igem.org/Part:BBa_K1216003 MainPage] - β-N-Acetylglucosaminidase (nagZ), BBa_K1216003 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert ______ into an red analog precipitate.<br>
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[http://parts.igem.org/Part:BBa_K1216006 Main Page] - Acetyl esterase (AES)with His-Tag and TEV cleavage site, BBa_K1216006 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert 5-Bromo-6-Chloro-3-indoxyl butyrate into an indigo analog precipitate <br> </p>
+
3. [http://parts.igem.org/Part:BBa_K1216006 Main Page] - Acetyl esterase (AES)with His-Tag and TEV cleavage site, BBa_K1216006 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert 5-Bromo-6-Chloro-3-indoxyl butyrate into an indigo analog precipitate <br> </p>
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[http://parts.igem.org/Part:BBa_K1216004 MainPage] - β-Glucuronidase (gusA)with HIS-Tag and TEV cleavage site, BBa_K1216004 :We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert ______ into an red analog precipitate.<br>
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4. [http://parts.igem.org/Part:BBa_K1216004 MainPage] - β-Glucuronidase (gusA)with HIS-Tag and TEV cleavage site, BBa_K1216004 :We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert ______ into an red analog precipitate.<br>
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Revision as of 18:44, 2 October 2013

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80px-Eth igem logo.png


Contents

Gene circuit

Our Favorite New Parts

1. [http://parts.igem.org/Part:BBa_K1216002 Main Page] - Acetyl esterase (AES), BBa_K1216002 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert 5-Bromo-6-Chloro-3-indoxyl butyrate into an indigo analog precipitate
2. [http://parts.igem.org/Part:BBa_K1216005 MainPage] - Alkaline phosphatase with His tag and TEV cleavage site (phoA), BBa_K1216002 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert 5-Bromo-6-Chloro-3-indoxyl butyrate into an indigo analog precipitate
3. [http://parts.igem.org/Part:BBa_K1216007 MainPage] - pLuxR1 mutated promoter, BBa_K1216007 : the promoter has an EC50 of 6.462 nM in liquid culture and 17'814nM on agar plates. This sensitivity is shifted 300'000 fold compared to the original BBa_R0062 pLuxR

Characterized Pre-existing Parts :

1. [http://parts.igem.org/Part:BBa_R0062:Experience Experience] - pLuxR wild type, BBa_R0062 : phoA gene from Citrobacter. We did Michealis-Menten kinetics of the phoA enzyme and also showed the conversion of PNP (para-nitrophenol phosphate) in a yellow analog precipitate.]
2. [http://parts.igem.org/Part:BBa_J61032:Experience Experience] - Alkaline phosphatase, BBa_J61032 : phoA gene originated from Citrobacter. We did Michealis-Menten kinetics of the phoA enzyme and also showed the conversion of PNP (para-nitrophenol phosphate) in a yellow analog precipitate


Characterized New Parts

1. [http://parts.igem.org/Part:BBa_K1216000 MainPage] - β-Glucuronidase (gusA), BBa_K1216000 :We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert ______ into an red analog precipitate.
2. [http://parts.igem.org/Part:BBa_K1216003 MainPage] - β-N-Acetylglucosaminidase (nagZ), BBa_K1216003 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert ______ into an red analog precipitate.
3. [http://parts.igem.org/Part:BBa_K1216006 Main Page] - Acetyl esterase (AES)with His-Tag and TEV cleavage site, BBa_K1216006 : We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert 5-Bromo-6-Chloro-3-indoxyl butyrate into an indigo analog precipitate

4. [http://parts.igem.org/Part:BBa_K1216004 MainPage] - β-Glucuronidase (gusA)with HIS-Tag and TEV cleavage site, BBa_K1216004 :We did Michealis-Menten kinetics with cell free extract and showed that the hydrolase can convert ______ into an red analog precipitate.