|
Resolution: standard / high Figure 4.
Experimental validation of 48 common bean 454-sequencing derived unigenes by RT-PCR. Lanes with 50 bp ladder are lanes 1, 20, 21, 40, 41, and 60; Confirmation of absence
of DNA contamination is shown in lanes 2-5 where RT-PCR amplification was carried
out with primers designed from contig11286 in lanes with genomic DNA, leaf cDNA, leaf
cDNA control (no reverse transcriptase added to reaction), and water as template to
check DNA contamination. In lanes 6-19, 22-39, and 42-56, 58 and 59 RT-PCR products
derived by amplification from an additional 47 common bean unigenes using leaf cDNA
as a template are shown (complete list of contigs shown in Table 4). Lane 57 is amplification
by the cons7 primers.
Kalavacharla et al. BMC Plant Biology 2011 11:135 doi:10.1186/1471-2229-11-135 |