{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["15"],"submitter":["Zhang Z"],"pubmed_abstract":["<h4>Background</h4>Orf, also known as contagious ecthyma (CE), is an acute, contagious zoonotic disease caused by the orf virus (ORFV). The F1L protein is a major immunodominant protein on the surface of ORFV and can induce the production of neutralizing antibodies.<h4>Methods</h4>The prokaryotic expression system was used to produce the recombinant F1L protein of ORFV, which was subsequently purified and used to immunize mice. Positive hybridoma clones were screened using an indirect enzyme-linked immunosorbent assay (ELISA). The reactivity and specificity of the monoclonal antibody (mAb) were verified through Western blot and indirect immunofluorescence (IFA). The linear antigenic epitope specific to the mAb was identified through Western blot, using truncated F1L proteins expressed in e"],"journal":["Frontiers in microbiology"],"pagination":["1373687"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11224485"],"repository":["biostudies-literature"],"pubmed_title":["Screening and characterization of a novel linear B-cell epitope on orf virus F1L protein."],"pmcid":["PMC11224485"],"pubmed_authors":["Yang Z","Zhang Z","Feng K","Zhang X","Zhang H","Li P","Yang T","Gong J","Ba S","Sun Z"],"additional_accession":[]},"is_claimable":false,"name":"Screening and characterization of a novel linear B-cell epitope on orf virus F1L protein.","description":"<h4>Background</h4>Orf, also known as contagious ecthyma (CE), is an acute, contagious zoonotic disease caused by the orf virus (ORFV). The F1L protein is a major immunodominant protein on the surface of ORFV and can induce the production of neutralizing antibodies.<h4>Methods</h4>The prokaryotic expression system was used to produce the recombinant F1L protein of ORFV, which was subsequently purified and used to immunize mice. Positive hybridoma clones were screened using an indirect enzyme-linked immunosorbent assay (ELISA). The reactivity and specificity of the monoclonal antibody (mAb) were verified through Western blot and indirect immunofluorescence (IFA). The linear antigenic epitope specific to the mAb was identified through Western blot, using truncated F1L proteins expressed in e","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024","modification":"2026-04-08T19:42:12.289Z","creation":"2026-04-08T14:07:11.274Z"},"accession":"S-EPMC11224485","cross_references":{"pubmed":["38974027"],"doi":["10.3389/fmicb.2024.1373687"]}}