(Submitter supplied) The unique cDNAs were PCR-amplified using Taq polymerase (Minotech, Heraklion, Greece) with the primers (pDNR-F, 2: 5'-CCGCATAACTTCGTATAGC–3' and pDNR-R, 2: 5'-CATGTTCACTTACCTACTGG-3') positioned by the polylinker site. The PCR products were purified using Nucleofast 96 columns (Macherey-Nagel, Duren, Germany). Approximately 3 μg of purified PCR product was placed in 384-well printing plates (Genetix, Hampshire, UK), dried in room temperature and resuspended in printing buffer containing 450 mM NaCl, 45 mM phosphate pH 7.0, 5% [v/v] formamide and 0.01% [v/v] maltoside at a final concentration of 200 μg/μl.
more...- Organism:
- Olea europaea
- 3 Series
- 76 Samples
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