Figure 4From: A new method to identify flanking sequence tags in chlamydomonas using 3’-RACEVerification of selected insertions using genomic PCR (HotStart Phusion). The DNA and primer pair used in each amplification are indicated at the top of the figure. The 100 bp ladder is loaded in the center and outermost lanes; the size of some of its bands is indicated on the left.Back to article page