<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mariotti S</submitter><funding>North Atlantic Treaty Organization</funding><funding>Istituto Superiore di Sanità</funding><funding>Italian Ministry of Defense</funding><pagination>610</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9953266</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(2)</volume><pubmed_abstract>The emergence of the new pathogen SARS-CoV-2 determined a rapid need for monoclonal antibodies (mAbs) to detect the virus in biological fluids as a rapid tool to identify infected individuals to be treated or quarantined. The majority of commercially available antigenic tests for SARS-CoV-2 rely on the detection of N antigen in biologic fluid using anti-N antibodies, and their capacity to specifically identify subjects infected by SARS-CoV-2 is questionable due to several structural analogies among the N proteins of different coronaviruses. In order to produce new specific antibodies, BALB/c mice were immunized three times at 20-day intervals with a recombinant spike (S) protein. The procedure used was highly efficient, and 40 different specific mAbs were isolated, purified and characteriz</pubmed_abstract><journal>Biomedicines</journal><pubmed_title>New Monoclonal Antibodies Specific for Different Epitopes of the Spike Protein of SARS-CoV-2 and Its Major Variants: Additional Tools for a More Specific COVID-19 Diagnosis.</pubmed_title><pmcid>PMC9953266</pmcid><funding_grant_id>intramural funds</funding_grant_id><funding_grant_id>Emerging Security Challenges Division Science for Peace and Security Programme 2020: NO-COVID: New and validated tools for the diagnosis and follow-up of SARS-CoV-2 infected indi-viduals grant # G5817</funding_grant_id><funding_grant_id>Real-Biodefense, grant# a2018.92</funding_grant_id><pubmed_authors>Michelini Z</pubmed_authors><pubmed_authors>Mariotti S</pubmed_authors><pubmed_authors>Marchi A</pubmed_authors><pubmed_authors>Bucci P</pubmed_authors><pubmed_authors>Capocefalo A</pubmed_authors><pubmed_authors>Gioacchini S</pubmed_authors><pubmed_authors>Negri D</pubmed_authors><pubmed_authors>Chiantore MV</pubmed_authors><pubmed_authors>Cara A</pubmed_authors><pubmed_authors>Di Bonito P</pubmed_authors><pubmed_authors>Iacobino A</pubmed_authors><pubmed_authors>D'Amelio R</pubmed_authors><pubmed_authors>Teloni R</pubmed_authors><pubmed_authors>Magurano F</pubmed_authors><pubmed_authors>Brouwer PJM</pubmed_authors><pubmed_authors>Grasso F</pubmed_authors><pubmed_authors>Borghi M</pubmed_authors><pubmed_authors>Baggieri M</pubmed_authors><pubmed_authors>Di Virgilio A</pubmed_authors><pubmed_authors>Sandini S</pubmed_authors><pubmed_authors>Nisini R</pubmed_authors><pubmed_authors>Acchioni C</pubmed_authors><pubmed_authors>Sgarbanti M</pubmed_authors></additional><is_claimable>false</is_claimable><name>New Monoclonal Antibodies Specific for Different Epitopes of the Spike Protein of SARS-CoV-2 and Its Major Variants: Additional Tools for a More Specific COVID-19 Diagnosis.</name><description>The emergence of the new pathogen SARS-CoV-2 determined a rapid need for monoclonal antibodies (mAbs) to detect the virus in biological fluids as a rapid tool to identify infected individuals to be treated or quarantined. The majority of commercially available antigenic tests for SARS-CoV-2 rely on the detection of N antigen in biologic fluid using anti-N antibodies, and their capacity to specifically identify subjects infected by SARS-CoV-2 is questionable due to several structural analogies among the N proteins of different coronaviruses. In order to produce new specific antibodies, BALB/c mice were immunized three times at 20-day intervals with a recombinant spike (S) protein. The procedure used was highly efficient, and 40 different specific mAbs were isolated, purified and characteriz</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-04-08T14:36:39.682Z</modification><creation>2024-11-20T08:07:05.729Z</creation></dates><accession>S-EPMC9953266</accession><cross_references><pubmed>36831149</pubmed><doi>10.3390/biomedicines11020610</doi></cross_references></HashMap>