I am thinking about making gateway vectors as well, and saw that
Terry Murphy at the Carnegie institute has made a few that will be
available to the community soon. Did you get any input on this note
you posted last october on flybase?
ref: news.indiana.edu bionet.drosophila:148
We're wondering if there is any experience using p element
transformation vectors (for example pUAST) made by gateway cloning
(invitrogen). Is there any difference in expression or mobilization
from a p-element having the 20-odd basepair recombination site
internally in the polylinker? We are making p-element transformation
plasmids this way, but would like to know if we are getting ourselves
Thanks for lettling me know!
University of Utah
20 N. 1900 East, Rm. 211
Salt Lake City , UT 84132-3201
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