<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pandey R</submitter><funding>Advancing a Healthier Wisconsin Endowment</funding><funding>NHLBI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>102036</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11098693</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>104(5)</volume><pubmed_abstract>Arterioles are key determinants of the total peripheral vascular resistance, which, in turn, is a key determinant of arterial blood pressure. However, the amount of protein available from one isolated human arteriole may be less than 5 μg, making proteomic analysis challenging. In addition, obtaining human arterioles requires manual dissection of unfrozen clinical specimens. This limits its feasibility, especially for powerful multicenter clinical studies in which clinical specimens need to be shipped overnight to a research laboratory for arteriole isolation. We performed a study to address low-input, test overnight tissue storage and develop a reference human arteriolar proteomic profile. In tandem mass tag proteomics, use of a booster channel consisting of human induced pluripotent stem</pubmed_abstract><journal>Laboratory investigation; a journal of technical methods and pathology</journal><pubmed_title>Proteomic Profiles of Human Arterioles Isolated From Fresh Adipose Tissue or Following Overnight Storage.</pubmed_title><pmcid>PMC11098693</pmcid><funding_grant_id>HL149620</funding_grant_id><funding_grant_id>R38 HL167238</funding_grant_id><funding_grant_id>HL144098</funding_grant_id><funding_grant_id>K24 HL152143</funding_grant_id><funding_grant_id>K24152143</funding_grant_id><funding_grant_id>P01 HL149620</funding_grant_id><funding_grant_id>HL121233</funding_grant_id><funding_grant_id>R38 HL143561</funding_grant_id><funding_grant_id>R01 HL144098</funding_grant_id><funding_grant_id>R01 HL121233</funding_grant_id><pubmed_authors>Pereckas M</pubmed_authors><pubmed_authors>Roberts ML</pubmed_authors><pubmed_authors>Jensen D</pubmed_authors><pubmed_authors>Liang M</pubmed_authors><pubmed_authors>Greene AS</pubmed_authors><pubmed_authors>Pandey R</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Widlansky ME</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proteomic Profiles of Human Arterioles Isolated From Fresh Adipose Tissue or Following Overnight Storage.</name><description>Arterioles are key determinants of the total peripheral vascular resistance, which, in turn, is a key determinant of arterial blood pressure. However, the amount of protein available from one isolated human arteriole may be less than 5 μg, making proteomic analysis challenging. In addition, obtaining human arterioles requires manual dissection of unfrozen clinical specimens. This limits its feasibility, especially for powerful multicenter clinical studies in which clinical specimens need to be shipped overnight to a research laboratory for arteriole isolation. We performed a study to address low-input, test overnight tissue storage and develop a reference human arteriolar proteomic profile. In tandem mass tag proteomics, use of a booster channel consisting of human induced pluripotent stem</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2025-07-03T03:04:55.369Z</modification><creation>2025-07-03T03:04:55.369Z</creation></dates><accession>S-EPMC11098693</accession><cross_references><pubmed>38408704</pubmed><doi>10.1016/j.labinv.2024.102036</doi></cross_references></HashMap>