<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Daniel Eriksson</submitter><study_type>proteomic profiling by array</study_type><organism>Homo sapiens</organism><species>Homo sapiens</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-14920</full_dataset_link><description>Paraneoplastic pemphigus is an autoimmune mucocutaneous blistering disease. It is caused by an autoimmune reaction in patients with a malignant neoplasms. We here used proteome arrays to perform a comprehensive study of autoimmune targets in paraneoplastic pemphigus, anti-p200 pemphigoid (Ap200P), and healthy controls. Solid phase protein arrays featuring more than 9000 full-length human proteins (ProtoArray v5.1, PAH05251020, ThermoFisher, Waltham, Mass) were screened with diluted 1:2000 sera from patients affected by paraneoplastic pemphigus, Ap200P, and healthy controls. Formed immunocomplexes were detected with a secondary antibody fluorescent signal (Alexa Fluor 647 goat anti-human IgG, A21445, ThermoFisher). Manufacturer’s protocol was followed using recommended reagents: ProtoArray Blocking Buffer Kit (PA055, ThermoFisher), Dylight 550 goat anti-GST (#DY550011-13-001), Cayman chemicals, Ann Arbor, Mich). Microarrays were scanned using the LuxScan HT24 (BioCapital) scanner.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Hybridization - -</sample_protocol><sample_protocol>Scaning - Microarrays were scanned using the LuxScan HT24 (BioCapital) scanner.</sample_protocol><sample_protocol>Labeling - -</sample_protocol><sample_protocol>Nucleic Acid Extraction - -</sample_protocol><sample_protocol>Sample Collection - Blood sampling. Serum extraction.</sample_protocol><sample_protocol>Growth Protocol - -</sample_protocol><sample_protocol>Sample Treatment - -</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>MAGE-TAB Files</figure_sub><figure_sub>Array Designs</figure_sub><pubmed_authors>Daniel Eriksson</pubmed_authors><data_protocol>Data Transformation - -</data_protocol></additional><is_claimable>false</is_claimable><name>PNP and ALG1 vs. healthy controls</name><description>Paraneoplastic pemphigus is an autoimmune mucocutaneous blistering disease. It is caused by an autoimmune reaction in patients with a malignant neoplasms. We here used proteome arrays to perform a comprehensive study of autoimmune targets in paraneoplastic pemphigus, anti-p200 pemphigoid (Ap200P), and healthy controls. Solid phase protein arrays featuring more than 9000 full-length human proteins (ProtoArray v5.1, PAH05251020, ThermoFisher, Waltham, Mass) were screened with diluted 1:2000 sera from patients affected by paraneoplastic pemphigus, Ap200P, and healthy controls. Formed immunocomplexes were detected with a secondary antibody fluorescent signal (Alexa Fluor 647 goat anti-human IgG, A21445, ThermoFisher). Manufacturer’s protocol was followed using recommended reagents: ProtoArray Blocking Buffer Kit (PA055, ThermoFisher), Dylight 550 goat anti-GST (#DY550011-13-001), Cayman chemicals, Ann Arbor, Mich). Microarrays were scanned using the LuxScan HT24 (BioCapital) scanner.</description><dates><release>2025-12-07T00:00:00Z</release><modification>2025-12-07T12:04:21.562Z</modification><creation>2025-03-07T17:56:15.139Z</creation></dates><accession>E-MTAB-14920</accession><cross_references><EFO>EFO_0002944</EFO><EFO>EFO_0003814</EFO><EFO>EFO_0003813</EFO><EFO>EFO_0003789</EFO><EFO>EFO_0002765</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0003815</EFO><EFO>EFO_0003969</EFO></cross_references></HashMap>