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Team:UNAM-Genomics Mexico/Collaboration
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==Locally-hosted documentation== | ==Locally-hosted documentation== | ||
| - | Since it is a requirement, we present here an overview of our collaborations with other iGEM teams. | + | Since it is a requirement, we present here an overview of our collaborations with other iGEM teams, all of them were very useful and enriched our iGEM experience. We appreciate their unvaluable help. |
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===Edinburgh=== | ===Edinburgh=== | ||
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===Cambridge=== | ===Cambridge=== | ||
| - | The Cambridge collaboration was mostly one-way. They've really helped us with parts we were unable to obtain. | + | The Cambridge collaboration was mostly one-way. They've really helped us with parts we were unable to obtain. We contacted them in July and during the next months we were following their progress with the Lux operon from Vibrio fischeri and other luciferases. After we failed trying to obtain the LuxAB genes ligated to a constitutive promoter, we again contacted them at the ends of September and they kindly sent us the following parts: |
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| + | '''Shipment:From Cambridge to Mexico''' | ||
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| + | '''October 2010''' | ||
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| + | 1.enhanced Photinus pyralis luciferase (EPIC) and P. pyralis LRE with no promoter. | ||
| + | 2.enhanced Photinus pyralis luciferase (EPIC) and P. pyralis LRE under pBad promoter. | ||
| + | 3.Luciola cruciata luciferase and L. cruciata LRE with no promoter. | ||
| + | 4.Luciola cruciata luciferase and L. cruciata LRE under pBad promoter. | ||
Revision as of 16:44, 27 October 2010
Locally-hosted documentation
Since it is a requirement, we present here an overview of our collaborations with other iGEM teams, all of them were very useful and enriched our iGEM experience. We appreciate their unvaluable help.
Edinburgh
The Illuminati connection proved to be an effective bridge. Parts, ideas, references and experiences were exchanged. We started the communication in July and since then we were sharing our projects progress by E-mail. In order to improve the success of our projects we interchanged different parts, as is described below.
Shipments:Sharing Parts
From Edinburgh to Mexico
May 2010
The Edinburgh’s advisor, Dr. Chris, kindly sent us LuxAB and LuxCDE PCR products and a plasmid containing the YFP protein:Lumazine.
October 2010
Dr.Chris sent us a second shipment consisting of the following parts:
Plasmids with luxAB genes, lumP gene encoding lumazine protein, luxAB and lumP ligated, luxCDE encoding substrate synthesis system for bacterial luciferase (XbaI site removed by mutation), BBa_K098101 (phycobilin synthesis genes with terminator),BBa_K098010 (phycobilin synthesis genes but with terminator removed), BBa_K191004 (RFP reporter plasmid for LOV-Tap blue light sensor), cph8 red light sensor derived from BBa_M30109.
From Mexico to Edinburgh
September 2010
We share with Edinburh team principally our synthesised parts, we sent them PCR amplified products containing green light photosensor CcaS and CcaR response regulator, blue light photosensor LovTAP and YFP protein from the Mr. Gene plasmids. As well we sent them a plasmid with our blue light reduced inducible promoter, a PCR amplified product containing light emitting luciferase genes LuxAB from Vibrio Fischeri and LovTAP ligated to four constitutive promoters: J23102,J23105, J23114 and J23117.
Cambridge
The Cambridge collaboration was mostly one-way. They've really helped us with parts we were unable to obtain. We contacted them in July and during the next months we were following their progress with the Lux operon from Vibrio fischeri and other luciferases. After we failed trying to obtain the LuxAB genes ligated to a constitutive promoter, we again contacted them at the ends of September and they kindly sent us the following parts:
Shipment:From Cambridge to Mexico
October 2010
1.enhanced Photinus pyralis luciferase (EPIC) and P. pyralis LRE with no promoter. 2.enhanced Photinus pyralis luciferase (EPIC) and P. pyralis LRE under pBad promoter. 3.Luciola cruciata luciferase and L. cruciata LRE with no promoter. 4.Luciola cruciata luciferase and L. cruciata LRE under pBad promoter.
UNAM-Cinvestav
This collaboration with our "brother" team on the main campus consists of Modelling aiding.
Full documentation
The full documentation on each collaboration is documented in other servers.
Edinburgh
Our team has recently established contact with Edinburgh's Illuminati team. Given that both projects are strikingly similar, and the good-natured collaboration between both teams, we decided to work together. Thus BRIDGING with people!
The following [http://openwetware.org/wiki/IGEM:UNAM-Genomics_Mexico/2009/Notebook/Collaborations Collaborations Log] will attempt to document the progress and facilitate communication between these teams.
Cambridge
Likewise, we are also working with the Cambridge team. Since they are interested in maximizing bioluminescent reactions, we are quite interested in their work ;) That collaboration is documented [http://openwetware.org/wiki/IGEM:UNAM-Genomics_Mexico/2009/Notebook/Collaborations.Cambridge here].
UNAM-Cinvestav
Model oriented stuff. Work still in progress...iGEM
iGEM is the International Genetically Engineered Machines Competition, held each year at MIT and organized with support of the Parts Registry. See more here.Synthetic Biology
This is defined as attempting to manipulate living objects as if they were man-made machines, specifically in terms of genetic engineering. See more here.Genomics
We are students on the Genomic Sciences program at the Center for Genomic Sciences of the National Autonomous University of Mexico, campus Morelos. See more here.This site is best viewed with a Webkit based Browser (eg: Google's Chrome, Apple's Safari),
Trident based (Microsoft's Internet Explorer) or Presto based (Opera) are not currently supported. Sorry.
