<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Thevendran R</submitter><funding>Technology Development Fund 1 grant of Ministry of Science, Technology and Innovation</funding><pagination>722</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10215423</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(5)</volume><pubmed_abstract>Dengue infection, caused by the dengue virus, is a global threat which requires immediate attention and appropriate disease management. The current diagnosis of dengue infection is largely based on viral isolation, RT-PCR and serology-based detection, which are time-consuming and expensive, and require trained personnel. For early diagnosis of dengue, the direct detection of a dengue antigenic target is efficacious, and one such target is NS1. NS1-based detection is primarily antibody-centric and is beset by drawbacks pertaining to antibodies such as the high cost of synthesis and large batch-to-batch variation. Aptamers are potential surrogates of antibodies and are much cheaper, without exhibiting batch-to-batch variation. Given these advantages, we sought to isolate RNA aptamers against</pubmed_abstract><journal>Biology</journal><pubmed_title>The Diagnostic Potential of RNA Aptamers against the NS1 Protein of Dengue Virus Serotype 2.</pubmed_title><pmcid>PMC10215423</pmcid><funding_grant_id>TDF03211027</funding_grant_id><pubmed_authors>Leighton G</pubmed_authors><pubmed_authors>Tang TH</pubmed_authors><pubmed_authors>Citartan M</pubmed_authors><pubmed_authors>Mutombwera A</pubmed_authors><pubmed_authors>Thevendran R</pubmed_authors><pubmed_authors>Rogini S</pubmed_authors><pubmed_authors>Shigdar S</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Diagnostic Potential of RNA Aptamers against the NS1 Protein of Dengue Virus Serotype 2.</name><description>Dengue infection, caused by the dengue virus, is a global threat which requires immediate attention and appropriate disease management. The current diagnosis of dengue infection is largely based on viral isolation, RT-PCR and serology-based detection, which are time-consuming and expensive, and require trained personnel. For early diagnosis of dengue, the direct detection of a dengue antigenic target is efficacious, and one such target is NS1. NS1-based detection is primarily antibody-centric and is beset by drawbacks pertaining to antibodies such as the high cost of synthesis and large batch-to-batch variation. Aptamers are potential surrogates of antibodies and are much cheaper, without exhibiting batch-to-batch variation. Given these advantages, we sought to isolate RNA aptamers against</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-04T19:29:47.684Z</modification><creation>2025-04-04T19:29:47.684Z</creation></dates><accession>S-EPMC10215423</accession><cross_references><pubmed>37237536</pubmed><doi>10.3390/biology12050722</doi></cross_references></HashMap>