Design and order your oligos according to
Oligonucleotide ordering tips: Standard de-salted oligos (usually the most inexpensive synthesis) are sufficient for cloning. If not already resuspended, dilute each oligo to 100 μM in DNAse-free water. Important: Don't order oligo synthesis in TE buffer, the buffer will interfere with the cloning process!
The shRNA oligos are annealed and cloned to TRC library vector
New! We have added a
The clones can be submitted directly to
If you use a clone from the GBU in your publication, please acknowledge us in the following way:
“shRNA constructs were generated by the Genome Biology Unit supported by HiLIFE, Faculty of Biological and Environmental Sciences, University of Helsinki, and Biocenter Finland"
Please also cite the creators of the vector backbone of your construct: