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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.

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