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ppl12148-sup-0001-TableS1.docWord document31KTable S1: Primers and probes used for qRT-PCR analyses of target genes.
ppl12148-sup-0002-FigureS1.docWord document194KFig. S1: cDNA and deduced amino acid sequence of isolated rice Osr9-LOX1 gene. Region used for antisense transformation is underlined.
ppl12148-sup-0003-FigureS2.docWord document647KFig. S2: Rice transformation vector pCAMBIA-as-r9LOX (13.4 kb) with hgh and gus as plant selectable marker genes (A) and transformation vector pr9LOX1-GFP (B) used to determine subcellular localization of Osr9-LOX1.
ppl12148-sup-0004-FigureS3.docWord document44KFig. S3: DNA gel-blot analysis of as-r9lox1 T2 lines (L54, L182 and L219) and one WT plant. Genomic DNA was digested with XbaI and EcoRI. Blots were hybridized with a probe specific for the gus reporter gene. All three as-r9lox1 lines, L54, L182 and L219, have a single T-DNA insertion.
ppl12148-sup-0005-FigureS4.docWord document35KFig. S4: Growth phenotypes of as-r9lox1 lines and WT plants (5-day-old seedlings).

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