Plant transformation vector with 9 myc tag.

[Hai Li]

Dear Colleagues:

We are pleased to announce the release of this plant transformation 
vector, pKYLX-myc9-loxP, to the ABRC at Ohio State University.

The vector, used in recent paper from our lab (Guo, H., and Ecker, 
J.R. (2003). Plant responses to ethylene gas are mediated by 
SCF(EBF1/EBF2)-dependent proteolysis of EIN3 transcription factor. 
Cell 115, 667-677.) can be recombined  in vitro to rapidly create 
myc fusions  to any of the 12000 SSP ORFs (http:/signal.salk.edu), by 
using Cre Recombinase.

A variety of other vectors for 2-hyb,  GST- and His-tag in E.  coli, 
as well as HA, Flag tag etc. are  available from Dr. Steve Elledge 
Lab (selledge at genetics.med.harvard.edu) with no MTA need.  In 
addition, a GST-CRE plasmid  is also  available to  make a life time 
supply of the Cre Recombinase enzyme in a 1 step purification method.

Please contact ABRC at Ohio State University for the pKYLX-myc9-loxp 
plasmid and its map.

Hai Li, Ph.D.
Joseph R. Ecker Lab
Plant Biology Laboratory
Salk Institute for Biological Studies
10010 North Torrey Pines Road
La Jolla, CA 92037