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* [[References]]
 
* [[References]]
  
We are currently preparing a methods paper describing the Tol2kit.
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We are currently preparing a methods paper describing the Tol2kit. If you have questions or comments, please post them on the
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[http://tol2kit.blogspot.com Tol2kit blog].
  
 
== Links ==
 
== Links ==

Revision as of 13:05, 2 February 2007

The Tol2kit

Tol2kit v1.0, released February 2007

Generating stable transgenic zebrafish lines has historically been laborious, for three reasons:

  • Building transgenesis constructs by conventional subcloning can be difficult, especially when using long coding or regulatory sequences
  • Injecting plasmid DNA yields mosaic transient expression and low germline transgenesis rates
  • When screening for stable integrations, transgenes that express fluorescent proteins (e.g. GFP) are easy to detect, but other transgenes are not.

The Tol2kit uses site-specific recombination-based cloning (multisite Gateway technology) to allow quick, modular assembly of promoter-coding sequence-3' tag constructs in a Tol2 transposon backbone.

It includes a variety of widely-useful entry clones, including hsp70 and beta-actin promoters; cytoplasmic, nuclear, and membrane-localized fluorescent proteins; and IRES-driven GFP cassettes for bicistronic expression. It includes two Tol2-based destination vector, one with a cmlc2:egfp transgenesis marker.

About this site

This wiki provides the documentation for the Tol2kit; it is maintained by the Chien lab. Please bear with us; it went live on 28 January and there are still many sections that are under construction.

We are currently preparing a methods paper describing the Tol2kit. If you have questions or comments, please post them on the Tol2kit blog.

Links

Wiki help

Consult the User's Guide for information on using the wiki software.