<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Junya Mizoi</submitter><study_type>transcription profiling by array</study_type><organism>Solanum lycopersicum</organism><species>Solanum lycopersicum</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16411</full_dataset_link><description>To investigate gene expression changes in tomato under low-phosphate conditions, plants were grown hydroponically using either a standard nutrient solution containing normal phosphate levels or a modified solution in which phosphate concentration was reduced to 1% of the control. Leaves were harvested two weeks after transplantation, and total RNA was extracted for microarray-based comparison of gene expression between the two phosphate regimes.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sample Collection - Leaf blades were cut from the plants, and the samples were frozen in liquid nitrogen.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was isolated from the frozen samples using RNA iso plus (TaKaRa). Three seedlings were pooled to prepare an RNA sample.</sample_protocol><sample_protocol>Growth Protocol - Tomato seedlings were transplanted at the age of 4 w old and grown for 2 w hydroponically with different concentrations of nutrients. The phosphate concentration in the control solution (P100%) and low phosphate solution (P1%) were 100% and 1%, respectively.</sample_protocol><sample_protocol>Hybridization - Two sets of samples (biological repeats) were analyzed using a Cy3 and Cy5 dye swap (technical repeats).</sample_protocol><sample_protocol>Labeling - Total RNA (250 ng) was labeled with a Low RNA Input Linear Amplification/Labeling Kit (Agilent Technologies) according to the manufacturer's instructions.</sample_protocol><sample_protocol>Scaning - Microarray slides were scanned (scanner model G2505C with scan control software, version A.8.4; Agilent Technologies) and the data were analyzed using Feature Extraction software, version 11.5.1.1 (Agilent technologies) using the default settings.</sample_protocol><figure_sub>MIAME Score</figure_sub><figure_sub>Raw Data</figure_sub><figure_sub>Organization</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><figure_sub>Array Designs</figure_sub><pubmed_authors>Junya Mizoi</pubmed_authors><data_protocol>Data Transformation - Data was processed using the Subio Platform software. Normalization was done by selecting LOWESS Normalization. One representative probe was selected for each locus.</data_protocol></additional><is_claimable>false</is_claimable><name>Microarray analysis of tomato leaves grown hydroponically under low-phosphate condition</name><description>To investigate gene expression changes in tomato under low-phosphate conditions, plants were grown hydroponically using either a standard nutrient solution containing normal phosphate levels or a modified solution in which phosphate concentration was reduced to 1% of the control. Leaves were harvested two weeks after transplantation, and total RNA was extracted for microarray-based comparison of gene expression between the two phosphate regimes.</description><dates><release>2026-01-06T00:00:00Z</release><modification>2026-05-27T16:14:22.784Z</modification><creation>2025-12-18T11:30:05.064Z</creation></dates><accession>E-MTAB-16411</accession><cross_references><Biostudies>E-MTAB-16410</Biostudies><EFO>EFO_0002768</EFO><EFO>EFO_0002944</EFO><EFO>EFO_0003814</EFO><EFO>EFO_0003813</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003815</EFO></cross_references></HashMap>