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('''The Tol2kit''')
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* [[Basic Gateway principles]]
 
* [[Basic Gateway principles]]
 
* [[List of entry and destination vectors]]
 
* [[List of entry and destination vectors]]
 +
* [[Protocols]]
 
* [[Components used for the Tol2kit]]
 
* [[Components used for the Tol2kit]]
 
* [[Sample results with the Tol2kit]]
 
* [[Sample results with the Tol2kit]]

Revision as of 00:17, 2 February 2007

The Tol2kit

Tol2kit v1.0, released January 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.

We are currently preparing a methods paper describing the Tol2kit.

Links

Wiki help

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