febs12140-sup-0001-TableS1-S5-DocS1-FigS1-S2.zipZip archive718K

Table S1. Spot reports obtained from the analysis of the two-dimensional maps of seed exudates.

Table S2. List of the identified proteins by LC-ESI-MS/MS and bioinformatcs analyses.

Table S3. Chitinase activities of exudates following incubation at 20 °C for 24 h.

Doc. S1. Quantitative PCR set-up and the results of the assessment of experimental conditions.

Table S4. Nucleotide sequences and specifications of primers probes used in quantitative RT-PCR for amplification of analyzed transcripts.

Table S5. Coefficients of the regression lines for each primer pairs according to the formula y = mx + q.

Fig. S1. Post-amplification melting curves of the amplicons obtained using the selected primer pairs in RT-PCR.

Fig. S2. Standard curves of dilution series of lupin genomic DNA amplified with the selected primer pairs.

Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.