<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Falco M</submitter><funding>Instituto de Salud Carlos III</funding><pagination>107-118</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9544867</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>100(2)</volume><pubmed_abstract>Killer immunoglobulin-like receptor (KIR) genes code for a family of inhibitory and activating receptors, finely tuning NK cell function. Numerous studies reported the relevance of KIR allelic polymorphism on KIR expression, ligand affinity, and strength in signal transduction. Although KIR variability, including gene copy number and allelic polymorphism, in combination with HLA class I polymorphism, impacts both KIR expression and NK cell education, only a precise phenotypic analysis can define the size of the different KIR&lt;sup>pos&lt;/sup> NK cell subsets. In this context, reagents recognizing a limited number of KIRs is essential. In this study, we have characterized the specificity of an anti-KIR mAb termed HP-DM1. Testing its binding to HEK-293T cells transfected with plasmids coding for</pubmed_abstract><journal>HLA</journal><pubmed_title>Epitope characterization of a monoclonal antibody that selectively recognizes KIR2DL1 allotypes.</pubmed_title><pmcid>PMC9544867</pmcid><funding_grant_id>AIRC 5 × 1000 2018 id. 21147</funding_grant_id><funding_grant_id>FIS00/0181</funding_grant_id><funding_grant_id>H2020‐MSCA‐ITN‐2017‐765104‐MATURE‐NK</funding_grant_id><pubmed_authors>Falco M</pubmed_authors><pubmed_authors>Muntasell A</pubmed_authors><pubmed_authors>Lopez-Botet M</pubmed_authors><pubmed_authors>Alicata C</pubmed_authors><pubmed_authors>Bottino C</pubmed_authors><pubmed_authors>Pende D</pubmed_authors><pubmed_authors>Moretta L</pubmed_authors><pubmed_authors>Meazza R</pubmed_authors><pubmed_authors>Canevali P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Epitope characterization of a monoclonal antibody that selectively recognizes KIR2DL1 allotypes.</name><description>Killer immunoglobulin-like receptor (KIR) genes code for a family of inhibitory and activating receptors, finely tuning NK cell function. Numerous studies reported the relevance of KIR allelic polymorphism on KIR expression, ligand affinity, and strength in signal transduction. Although KIR variability, including gene copy number and allelic polymorphism, in combination with HLA class I polymorphism, impacts both KIR expression and NK cell education, only a precise phenotypic analysis can define the size of the different KIR&lt;sup>pos&lt;/sup> NK cell subsets. In this context, reagents recognizing a limited number of KIRs is essential. In this study, we have characterized the specificity of an anti-KIR mAb termed HP-DM1. Testing its binding to HEK-293T cells transfected with plasmids coding for</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2026-05-31T16:08:28.166Z</modification><creation>2025-02-19T01:28:08.78Z</creation></dates><accession>S-EPMC9544867</accession><cross_references><pubmed>35411634</pubmed><doi>10.1111/tan.14630</doi></cross_references></HashMap>