<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22</volume><submitter>Costa ADT</submitter><funding>Banco Nacional de Desenvolvimento Econômico e Social</funding><pubmed_abstract>Foodborne outbreaks caused by parasites have long been a public health issue. Among the available contamination detection methods, qPCR is one of the most sensitive and specific. However, it can be cumbersome and error-prone, if used by unexperienced users. Moreover, qPCR reagents usually require freezer temperatures for transportation and storage. We present a gelified reaction format that allows the reagents to be stored at 2-8 °C for up to 90 days without losing performance. The gelification process eliminates most operator mistakes during reaction setup, and renders the qPCR plates ready-to-use. The new reaction makeup was evaluated using artificially contaminated samples of distinct food matrices for sensitivity, specificity, repeatability, reproducibility, and stability. Samples cons</pubmed_abstract><journal>Food and waterborne parasitology</journal><pagination>e00111</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7930119</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ready-to-use qPCR for detection of &lt;i>Cyclospora cayetanensis&lt;/i> or &lt;i>Trypanosoma cruzi&lt;/i> in food matrices.</pubmed_title><pmcid>PMC7930119</pmcid><pubmed_authors>Pereira-Chioccola VL</pubmed_authors><pubmed_authors>Costa ADT</pubmed_authors><pubmed_authors>da Silva AJ</pubmed_authors><pubmed_authors>Rampazzo RCP</pubmed_authors><pubmed_authors>Pinto RS</pubmed_authors><pubmed_authors>Murphy HR</pubmed_authors><pubmed_authors>Krieger MA</pubmed_authors><pubmed_authors>Tassi W</pubmed_authors><pubmed_authors>Farias AB</pubmed_authors><pubmed_authors>Mattos EC</pubmed_authors><pubmed_authors>Jacomasso T</pubmed_authors><pubmed_authors>Marciano MAM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ready-to-use qPCR for detection of &lt;i>Cyclospora cayetanensis&lt;/i> or &lt;i>Trypanosoma cruzi&lt;/i> in food matrices.</name><description>Foodborne outbreaks caused by parasites have long been a public health issue. Among the available contamination detection methods, qPCR is one of the most sensitive and specific. However, it can be cumbersome and error-prone, if used by unexperienced users. Moreover, qPCR reagents usually require freezer temperatures for transportation and storage. We present a gelified reaction format that allows the reagents to be stored at 2-8 °C for up to 90 days without losing performance. The gelification process eliminates most operator mistakes during reaction setup, and renders the qPCR plates ready-to-use. The new reaction makeup was evaluated using artificially contaminated samples of distinct food matrices for sensitivity, specificity, repeatability, reproducibility, and stability. Samples cons</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2026-04-07T23:27:13.681Z</modification><creation>2021-03-09T08:18:11Z</creation></dates><accession>S-EPMC7930119</accession><cross_references><pubmed>33681489</pubmed><doi>10.1016/j.fawpar.2021.e00111</doi></cross_references></HashMap>