aligning promoter regions to find a binding site - (Oct/16/2008 )
Hi everyone,
I have purified a transcription factor and have observed a band shift with a promoter region for a gene in Staphylococcus as well as its homologue in a different species. Is there a way that I could align the 2 probes to attempt to identify the binding site?
Any ideas much appreciated
-bench buddy-
hello bench buddy,
after you have sequenced your bands you can perform a blast2seq from ncbi. just go to this page and paste your sequences
http://blast.ncbi.nlm.nih.gov/bl2seq/wblast2.cgi
cheers.
-toejam-
Thanks toejam,
will give that a go.
Much appreciated.
QUOTE (toejam @ Oct 16 2008, 05:26 AM)
hello bench buddy,
after you have sequenced your bands you can perform a blast2seq from ncbi. just go to this page and paste your sequences
http://blast.ncbi.nlm.nih.gov/bl2seq/wblast2.cgi
cheers.
after you have sequenced your bands you can perform a blast2seq from ncbi. just go to this page and paste your sequences
http://blast.ncbi.nlm.nih.gov/bl2seq/wblast2.cgi
cheers.
-bench buddy-