OriC/ter ratio determination: Difference between revisions
(New page: This protocol describes how one can determine the ration of the origin of termination ''oriC'' and the terminus of replication ''ter'' in ''Escherichia coli''. That is for example importan...) |
No edit summary |
||
| Line 1: | Line 1: | ||
==Curators== | |||
'''[[User:Torsten Waldminghaus | Torsten Waldminghaus]]''' | |||
''Anyone should feel free to add themselves as a curator for this consensus protocol. You do not need to be a curator in order to contribute. The OpenWetWare community is currently [[OpenWetWare:Information management/Protocol curators|discussing the idea of protocol curators]]. Please contribute.'' | |||
==Abstract== | |||
This protocol describes how one can determine the ration of the origin of termination ''oriC'' and the terminus of replication ''ter'' in ''Escherichia coli''. That is for example important for [[cell cycle analysis]]. | This protocol describes how one can determine the ration of the origin of termination ''oriC'' and the terminus of replication ''ter'' in ''Escherichia coli''. That is for example important for [[cell cycle analysis]]. | ||
==Materials== | |||
List everything necessary to perform the protocol here. Include all information about suppliers, ordering details, etc. Links to the suppliers' page on that material are also appropriate and encouraged. Please be aware that users of this protocol may not be working in the same country as you. | |||
===Reagents=== | |||
Biological resources e.g. cell lines, buffers (link to a method for making them), enzymes, chemicals, kits, etc. | |||
===Equipment=== | |||
Any equipment used to perform the protocol (link to a method for using them). | |||
==Procedure== | |||
A step by step guide to the experimental procedure. | |||
If you find it helpfull you could use the following icons to highlight important parts: | |||
[[Image:Difficult step.png]] icon to highlight difficult steps | |||
[[Image:Critical step.png]] warn about critical steps | |||
[[Image:Time required.png]] help people plan how long steps will take | |||
[[Image:Pause point.png]] where protocol can be interrupted | |||
[[Image:Optional step.png]] steps that can be omitted or included | |||
==Critical steps== | |||
Referenced from the main protocol, a more thorough explanation of particularly important steps in the protocol. | |||
==Notes== | |||
Referenced from the main protocol, any comments about the protocol should be made here; i.e. how it was developed. Any comments added should be signed (by adding <nowiki>*'''~~~~''':</nowiki> in front) and explained. Links to FAQs/tips provided by other sources such as the manufacturer or other websites would be best made here.<br> | |||
Anecdotal observations that might be of use to others can also be posted here; e.g. 'my cells were still floating'.<br> | |||
==Discussion== | |||
You can [[Talk:{{PAGENAME}}|discuss this protocol]]. | |||
Tag this page with categories to allow easier indexing and searching. See [[Categories]] for information on existing categories. | |||
Revision as of 09:31, 26 February 2009
Curators
Anyone should feel free to add themselves as a curator for this consensus protocol. You do not need to be a curator in order to contribute. The OpenWetWare community is currently discussing the idea of protocol curators. Please contribute.
Abstract
This protocol describes how one can determine the ration of the origin of termination oriC and the terminus of replication ter in Escherichia coli. That is for example important for cell cycle analysis.
Materials
List everything necessary to perform the protocol here. Include all information about suppliers, ordering details, etc. Links to the suppliers' page on that material are also appropriate and encouraged. Please be aware that users of this protocol may not be working in the same country as you.
Reagents
Biological resources e.g. cell lines, buffers (link to a method for making them), enzymes, chemicals, kits, etc.
Equipment
Any equipment used to perform the protocol (link to a method for using them).
Procedure
A step by step guide to the experimental procedure.
If you find it helpfull you could use the following icons to highlight important parts:
icon to highlight difficult steps
warn about critical steps
help people plan how long steps will take
where protocol can be interrupted
steps that can be omitted or included
Critical steps
Referenced from the main protocol, a more thorough explanation of particularly important steps in the protocol.
Notes
Referenced from the main protocol, any comments about the protocol should be made here; i.e. how it was developed. Any comments added should be signed (by adding *'''~~~~''': in front) and explained. Links to FAQs/tips provided by other sources such as the manufacturer or other websites would be best made here.
Anecdotal observations that might be of use to others can also be posted here; e.g. 'my cells were still floating'.
Discussion
You can discuss this protocol.
Tag this page with categories to allow easier indexing and searching. See Categories for information on existing categories.
