I guess the first question would be how are you planning on assaying the
promoter activity? LacZ, GFP, nutritional marker....
If you already have an integrated reporter you might want to consider
recombining your promoter directly. Alternatively you could integrate a
reporter directly behind your promoter.
I would argue that promoters should always be assayed in a chromosomal
context, preferably in their native positions.
On 9/18/03 20:00, "Sreihani at aol.com" <Sreihani at aol.com> wrote:
>> I am in search of a promoter less yeast vector for my research. The purpose
> is to put the promoter of my interest in a yeast vector and look at the
> for my promoter activity. We were supposed to get a promoter less yeast
> vector by the name of pAS 201, but the company in charge was not able to
> the vector to us as promised. I have contacted the SGD at Stanford, and Dr.
> has suggested that I post my request on your site for possible response.
>> Thank you in advance.
YEAST bionet newsgroup see: http://www.bio.net/hypermail/YEAST/
YEAST e-mail: messages sent to yeast at net.bio.net
subscribe: mailto:biosci-server at net.bio.net and say: subscribe yeast
unsubscribe: mailto:biosci-server at net.bio.net and say: unsubscribe yeast
YEAST on the WWW: http://www.yeastgenome.org/VL-yeast.html
Newsgroup Moderator SGD Curators: yeast-biosci-moderator at yeastgenome.org