Team:DTU-Denmark/Wet lab

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!align="center" width="14%" style="border-collapse: separate; border-spacing: 0; border-width: 1px; border-style: solid; border-color: white;"|[[Team:DTU-Denmark/Modeling|<span style="color:white;">Modeling</span>]]
!align="center" width="14%" style="border-collapse: separate; border-spacing: 0; border-width: 1px; border-style: solid; border-color: white;"|[[Team:DTU-Denmark/Modeling|<span style="color:white;">Modeling</span>]]
!align="center" width="14%" style="border-collapse: separate; border-spacing: 0; border-width: 1px; border-style: solid; border-color: white;"|[[Team:DTU-Denmark/Wet_lab|Wet Lab]]
!align="center" width="14%" style="border-collapse: separate; border-spacing: 0; border-width: 1px; border-style: solid; border-color: white;"|[[Team:DTU-Denmark/Wet_lab|Wet Lab]]
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!align="center" width="14%" style="border-collapse: separate; border-spacing: 0; border-width: 1px; border-style: solid; border-color: white;"|[[Team:DTU-Denmark/Gallery|<span style="color:white;">Gallery</span]]
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!align="center" width="14%" style="border-collapse: separate; border-spacing: 0; border-width: 1px; border-style: solid; border-color: white;"|[[Team:DTU-Denmark/Gallery|<span style="color:white;">Gallery</span>]]
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= Anti-Terminator experimental setup =
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= Wetlab =
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On this page is described the experiences, procedures and protocols that we have used.
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Further the experimental process is described for the two parallel tracks, the repressor and terminator part, what have we experienced when working with our parts, and the BB standard.
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=== N-protein plasmid ===
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'''Protocols'''
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The N protein were isolated from salmonella genomic DNA with specific designed primers. We used the natural occurring RBS site, as a High expression of N have shown non specific anti-termination effect on a global scale on the genome. [[#References References]]
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For all the methods we have shaped the protocols to the standards and experiences of our lab.
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We have collected the protocols we used in a comprehensive list below where it is possible to read them in full length. They contain our procedure as well as references. Some time this might be weakly documented when given to us by communication with supervisors.
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=== References ===
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== General lab work "Materials and Methods" ==
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* NC Franklin, JH Doelling - Am Soc Microbiol "Overexpression of N antitermination proteins of bacteriophages lambda, 21, and P22: loss of N protein specificity." - Journal of bacteriology, 1989
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=== The Biobrick standard and 3A assemply ===
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== Repressor group ==
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== Terminator group ==
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XXXX here we should write a short abstract XXXX
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=== Work flow ===
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XXXX maybe show pictures of our work plan, or write it simplified - the more pictures the better XXX
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== Protocols ==
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== References and resources ==
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* [ if any]

Latest revision as of 20:35, 2 October 2010

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Home Team Project Parts Submitted to the Registry Modeling Wet Lab Gallery

Contents

Wetlab

On this page is described the experiences, procedures and protocols that we have used. Further the experimental process is described for the two parallel tracks, the repressor and terminator part, what have we experienced when working with our parts, and the BB standard.

Protocols For all the methods we have shaped the protocols to the standards and experiences of our lab. We have collected the protocols we used in a comprehensive list below where it is possible to read them in full length. They contain our procedure as well as references. Some time this might be weakly documented when given to us by communication with supervisors.

General lab work "Materials and Methods"

The Biobrick standard and 3A assemply

Repressor group

Terminator group

XXXX here we should write a short abstract XXXX

Work flow

XXXX maybe show pictures of our work plan, or write it simplified - the more pictures the better XXX

Protocols

References and resources

  • [ if any]