<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(3)</volume><submitter>Attanayake H</submitter><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Efficient real-time PCR kits are commercially available for the detection of &lt;i>Chlamydia trachomatis&lt;/i> (CT) genetic material, but at a price. As a result, cost-effective, sensitive and specific CT diagnostic tests are essential for resource limited countries. This study aims to describe the optimization of a loop mediated isothermal amplification (LAMP) assay for the detection of CT &lt;i>ompA&lt;/i> DNA in urine.&lt;h4>Methods&lt;/h4>Cost-saving modifications included using &lt;i>Bsm&lt;/i> polymerase and a nucleic acid gel stain. Crude DNA extraction (method-1) involved centrifuging urine at 14,000 g for 30 min, heating the deposit at 95 °C for 5 min, and centrifuging again at 17,000 &lt;i>g&lt;/i> for 1 min. To boost sensitivity, urinary inhibitors were diluted with phosphate-buffered sal</pubmed_abstract><journal>Advances in laboratory medicine</journal><pagination>314-319</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12446907</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Detection of &amp;lt;i&amp;gt;Chlamydia trachomatis ompA&amp;lt;/i&amp;gt; DNA in urine by loop-mediated isothermal amplification (LAMP) assay.</pubmed_title><pmcid>PMC12446907</pmcid><pubmed_authors>Elvitigala J</pubmed_authors><pubmed_authors>Abeygunasekera N</pubmed_authors><pubmed_authors>Goonasekara C</pubmed_authors><pubmed_authors>Gunasekera KM</pubmed_authors><pubmed_authors>Attanayake H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Detection of &amp;lt;i&amp;gt;Chlamydia trachomatis ompA&amp;lt;/i&amp;gt; DNA in urine by loop-mediated isothermal amplification (LAMP) assay.</name><description>&lt;h4>Objectives&lt;/h4>Efficient real-time PCR kits are commercially available for the detection of &lt;i>Chlamydia trachomatis&lt;/i> (CT) genetic material, but at a price. As a result, cost-effective, sensitive and specific CT diagnostic tests are essential for resource limited countries. This study aims to describe the optimization of a loop mediated isothermal amplification (LAMP) assay for the detection of CT &lt;i>ompA&lt;/i> DNA in urine.&lt;h4>Methods&lt;/h4>Cost-saving modifications included using &lt;i>Bsm&lt;/i> polymerase and a nucleic acid gel stain. Crude DNA extraction (method-1) involved centrifuging urine at 14,000 g for 30 min, heating the deposit at 95 °C for 5 min, and centrifuging again at 17,000 &lt;i>g&lt;/i> for 1 min. To boost sensitivity, urinary inhibitors were diluted with phosphate-buffered sal</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T17:01:35.038Z</modification><creation>2026-05-30T03:06:15.153Z</creation></dates><accession>S-EPMC12446907</accession><cross_references><pubmed>40977814</pubmed><doi>10.1515/almed-2024-0117</doi></cross_references></HashMap>