Team:Heidelberg/Notebook

From 2010.igem.org

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{{:Team:Heidelberg/Pagetop|notebook}}
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= Notebooks =
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This is a template page. READ THESE INSTRUCTIONS.
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You are provided with this team page template with which to start the iGEM season.  You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2008.igem.org/Help:Template/Examples">HERE</a>.
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You <strong>MUST</strong> have a team description page, a project abstract, a complete project description, a lab notebook, and a safety page.  PLEASE keep all of your pages within your teams namespace. 
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Welcome to our notebooks! Here you will find the documentation of our labwork in diary form. '''Just follow the links and look around!'''
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== [https://2010.igem.org/Team:Heidelberg/Notebook/miRNA_Kit Synthetic miRNA Kit] ==
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Dive into the depth of our Synthetic miRNA Kit! Explore the possibilites, retrace the development of its versatile parts, '''feel the creativity and start playing''' with them yourself!
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== [https://2010.igem.org/Team:Heidelberg/Notebook/Capsid_Shuffling Capsid shuffling] ==
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|You can write a background of your team here. Give us a background of your team, the members, etc. Or tell us more about something of your choosing.
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Did you ever get bored by the common viruses that infect randomly, irrational and uncontrolable? Never again! We created a library of synthetic viruses that can be evolved on any cell type of choice and enable you to '''select for your personal favourite virus, custom made!'''
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|[[Image:Heidelberg_logo.png|200px|right|frame]]
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''Tell us more about your project.  Give us background.  Use this is the abstract of your project.  Be descriptive but concise (1-2 paragraphs)''
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|[[Image:Heidelberg_team.png|right|frame|Your team picture]]
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|align="center"|[[Team:Heidelberg | Team Example]]
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<!--- The Mission, Experiments --->
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==== [https://2010.igem.org/Team:Heidelberg/Notebook/Capsid_Shuffling/Homology_Based Homology Based] ====
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This clever approach uses DNAseI '''shuffling of AAV capsid genes''' followed by PCR amplification with primers for homologous regions. Find out how we mastered this approach!
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==== [https://2010.igem.org/Team:Heidelberg/Notebook/Capsid_Shuffling/ViroBytes ViroBytes] ====
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!align="center"|[[Team:Heidelberg|Home]]
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Last year's Alberta BioBytes served as the basis for our '''ViroBytes''' method. We optimized the protocol for production of '''rationally shuffled synthetic viruses'''.
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!align="center"|[[Team:Heidelberg/Team|Team]]
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!align="center"|[https://igem.org/Team.cgi?year=2010&team_name=Heidelberg Official Team Profile]
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!align="center"|[[Team:Heidelberg/Project|Project]]
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!align="center"|[[Team:Heidelberg/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:Heidelberg/Modeling|Modeling]]
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!align="center"|[[Team:Heidelberg/Notebook|Notebook]]
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!align="center"|[[Team:Heidelberg/Safety|Safety]]
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== [https://2010.igem.org/Team:Heidelberg/Notebook/miMeasure miMeasure] ==
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'''THE''' standard for characterization of synthetic miRNA binding sites in mammalian cells!
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== [https://2010.igem.org/Team:Heidelberg/Notebook/Mouse_Infection ''in Vivo'' Study] ==
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Follow how we put our constructs into our viruses, and our viruses into mouse, showing how we can '''tune gene expression in vivo'''!
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==Notebook==
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== [https://2010.igem.org/Team:Heidelberg/Notebook/Material_Methods Materials & Methods] ==
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== [https://2010.igem.org/Team:Heidelberg/Notebook/Biosafety BioSafety] ==
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== [https://2010.igem.org/Team:Heidelberg/Notebook/Modeling Modeling] ==
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You should make use of the calendar feature on the wiki and start a lab notebook.  This may be looked at by the judges to see how your work progressed throughout the summer.  It is a very useful organizational tool as well.
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{{:Team:Heidelberg/Bottom}}

Latest revision as of 03:17, 27 October 2010

Notebooks

Welcome to our notebooks! Here you will find the documentation of our labwork in diary form. Just follow the links and look around!

Synthetic miRNA Kit

Dive into the depth of our Synthetic miRNA Kit! Explore the possibilites, retrace the development of its versatile parts, feel the creativity and start playing with them yourself!

Capsid shuffling

Did you ever get bored by the common viruses that infect randomly, irrational and uncontrolable? Never again! We created a library of synthetic viruses that can be evolved on any cell type of choice and enable you to select for your personal favourite virus, custom made!

Homology Based

This clever approach uses DNAseI shuffling of AAV capsid genes followed by PCR amplification with primers for homologous regions. Find out how we mastered this approach!

ViroBytes

Last year's Alberta BioBytes served as the basis for our ViroBytes method. We optimized the protocol for production of rationally shuffled synthetic viruses.

miMeasure

THE standard for characterization of synthetic miRNA binding sites in mammalian cells!

in Vivo Study

Follow how we put our constructs into our viruses, and our viruses into mouse, showing how we can tune gene expression in vivo!

Materials & Methods

BioSafety

Modeling

Contents