<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang X</submitter><funding>Shanghai Science&amp; Technology Innovation Action Program</funding><funding>Shanghai Public Health Clinical Center hospital-level scientific research project</funding><pagination>1530</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10177487</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(9)</volume><pubmed_abstract>Loop-mediated isothermal amplification (LAMP), as the rank one alternative to a polymerase chain reaction (PCR), has been widely applied in point-of-care testing (POCT) due to its rapid, simple, and cost-effective characteristics. However, it is difficult to achieve real-time monitoring and multiplex detection with the traditional LAMP method. In addition, these approaches that use turbidimetry, sequence-independent intercalating dyes, or pH-sensitive indicators to indirectly reflect amplification can result in false-positive results if non-specific amplification occurs. To fulfill the needs of specific target detection and one-pot multiplex detection, a variety of probe-based LAMP assays have been developed. This review focuses on the principles of these assays, summarizes their applicati</pubmed_abstract><journal>Diagnostics (Basel, Switzerland)</journal><pubmed_title>Evolution of the Probe-Based Loop-Mediated Isothermal Amplification (LAMP) Assays in Pathogen Detection.</pubmed_title><pmcid>PMC10177487</pmcid><funding_grant_id>KY -GW-2023-32</funding_grant_id><funding_grant_id>21Y11900500</funding_grant_id><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Zeng Y</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evolution of the Probe-Based Loop-Mediated Isothermal Amplification (LAMP) Assays in Pathogen Detection.</name><description>Loop-mediated isothermal amplification (LAMP), as the rank one alternative to a polymerase chain reaction (PCR), has been widely applied in point-of-care testing (POCT) due to its rapid, simple, and cost-effective characteristics. However, it is difficult to achieve real-time monitoring and multiplex detection with the traditional LAMP method. In addition, these approaches that use turbidimetry, sequence-independent intercalating dyes, or pH-sensitive indicators to indirectly reflect amplification can result in false-positive results if non-specific amplification occurs. To fulfill the needs of specific target detection and one-pot multiplex detection, a variety of probe-based LAMP assays have been developed. This review focuses on the principles of these assays, summarizes their applicati</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-22T00:33:23.392Z</modification><creation>2025-04-05T19:35:12.246Z</creation></dates><accession>S-EPMC10177487</accession><cross_references><pubmed>37174922</pubmed><doi>10.3390/diagnostics13091530</doi></cross_references></HashMap>