<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Nora Doleschall</submitter><organism>Homo sapiens</organism><software>Agilent Feature Extraction</software><software>None</software><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14718</full_dataset_link><description>This experiment was used to compare the miRNA expression profiles of paired healthy blood serum, blood plasma, blood-derived cellular components and their conditioned media.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Growth Protocol - Blood cellular components were collected from EDTA-anticoagulated whole blood after removing the plasma by centrifugation. These were washed twice with PBS then incubated in RPMI-1640 without FBS for 6 hours. WBCs as well as conditioned media were stored at – 80°C until RNA extraction.</sample_protocol><sample_protocol>Hybridization - Hybridisation was performed over 20 hours at 55 degrees C, rotating 20rpm in Agilent hybridisation oven</sample_protocol><sample_protocol>Sample Collection - Blood samples were taken via venepuncture, and were immediately transferred to the processing laboratory, where the cells and the supernatant – serum and EDTA-anticoagulated plasma – were separated by centrifugation. Serum and plasma aliquots were prepared, immediately frozen and stored at − 80 °C until the measurements were performed.</sample_protocol><sample_protocol>Labeling - Cy3-pCp labelling was performed according to Agilent recommendations</sample_protocol><sample_protocol>Scaning - Agilent Microarray Scanner (G2505C) was used for array scanning and Agilent Feature Extraction software used for image processing.</sample_protocol><sample_protocol>Nucleic Acid Extraction - smallRNA enriched RNA extraction was performed using Qiagen miRNeasy kit</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><data_protocol>Data Transformation - Agilent Feature Extraction software was used to assign probes to genes and to perform background correction and error evaluation for individual probes</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><instrument_platform>Agilent Microarray Scanner G2505C</instrument_platform><instrument_platform>Tabletop microfuge, Nanodrop</instrument_platform><instrument_platform>PC</instrument_platform><instrument_platform>Agilent Hybridisation Oven G2545A</instrument_platform><instrument_platform>Tabletop centrifuge</instrument_platform><instrument_platform>None</instrument_platform><study_type>microRNA profiling by array</study_type><species>Homo sapiens</species><pubmed_authors>László Cervenak</pubmed_authors><pubmed_authors>Nora Doleschall</pubmed_authors></additional><is_claimable>false</is_claimable><name>miRNA microarray experiment elucidating the contribution of intra-and extracellular leukocyte-derived miRNAs to paired blood serum and plasma samples</name><description>This experiment was used to compare the miRNA expression profiles of paired healthy blood serum, blood plasma, blood-derived cellular components and their conditioned media.</description><dates><release>2025-06-30T00:00:00Z</release><modification>2024-12-19T22:13:46.341Z</modification><creation>2024-12-19T22:13:46.341Z</creation></dates><accession>E-MTAB-14718</accession><cross_references><Biostudies>E-MTAB-14717</Biostudies><Biostudies>E-MTAB-14672</Biostudies><EFO>EFO_0002944</EFO><EFO>EFO_0003814</EFO><EFO>EFO_0000753</EFO><EFO>EFO_0003813</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003815</EFO></cross_references></HashMap>