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Viramed Biotech ce marked igm immunoblot assays
Ce Marked Igm Immunoblot Assays, supplied by Viramed Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ce+mark/anti+assays+ce+igm+immunoblot+marked/pmc13170342-147-5-9
Average 86 stars, based on 1 article reviews
ce marked igm immunoblot assays - by Bioz Stars, 2026-10
86/100 stars

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Related Articles

Enzyme-linked Immunosorbent Assay:

Article Title: Evaluation of standard and modified two-tiered testing algorithms using well-characterized early Lyme disease samples
Article Snippet: .. Serologic testing was performed using (i) a VlsE/pepC10 IgM/IgG ELISA (Zeus Scientific, Raritan, NJ), followed by IgM and IgG ViraStripe immunoblots (Viramed; Biotech AG, Germany) at Mayo Clinic (MC, Rochester, MN); and (ii) a C6 peptide ELISA (Oxford Immunotec, Marlborough, MA) performed at Stony Brook University (SB, Stony Brook, NY). ..

Article Title: Diagnostic potential for IgM antibody detection by the DPP Syphilis TnT assay in neonates at risk for congenital syphilis
Article Snippet: .. There are commercial IgM immunoblot and enzyme-linked immunosorbent assay (ELISA) assays used in Europe (e.g., ViraMed and Euroimmun, Germany), all of which are Conformité Européenne (CE) marked and therefore meet regulatory standards for in vitro diagnostics in the European market. .. Published data show that these CE-marked IgM immunoblot assays (ViraMed, Euroimmun) demonstrate strong diagnostic accuracy, with reported sensitivities ranging from 90.0% to 94.4% and specificities between 97.1% and 99.2% when evaluated against composite or reference standards in infants and neonates with suspected CS ( , ).

Western Blot:

Article Title: Evaluation of standard and modified two-tiered testing algorithms using well-characterized early Lyme disease samples
Article Snippet: .. Serologic testing was performed using (i) a VlsE/pepC10 IgM/IgG ELISA (Zeus Scientific, Raritan, NJ), followed by IgM and IgG ViraStripe immunoblots (Viramed; Biotech AG, Germany) at Mayo Clinic (MC, Rochester, MN); and (ii) a C6 peptide ELISA (Oxford Immunotec, Marlborough, MA) performed at Stony Brook University (SB, Stony Brook, NY). ..

Article Title: Diagnostic potential for IgM antibody detection by the DPP Syphilis TnT assay in neonates at risk for congenital syphilis
Article Snippet: There are commercial IgM immunoblot and enzyme-linked immunosorbent assay (ELISA) assays used in Europe (e.g., ViraMed and Euroimmun, Germany), all of which are Conformité Européenne (CE) marked and therefore meet regulatory standards for in vitro diagnostics in the European market. .. Published data show that these CE-marked IgM immunoblot assays (ViraMed, Euroimmun) demonstrate strong diagnostic accuracy, with reported sensitivities ranging from 90.0% to 94.4% and specificities between 97.1% and 99.2% when evaluated against composite or reference standards in infants and neonates with suspected CS ( , ). .. In contrast, the CE-marked Euroimmun IgM ELISA typically shows more modest sensitivity (≈60%) despite specificity approaching 100%.

Article Title: Diagnostic potential for IgM antibody detection by the DPP Syphilis TnT assay in neonates at risk for congenital syphilis
Article Snippet: .. There are commercial IgM immunoblot and enzyme-linked immunosorbent assay (ELISA) assays used in Europe (e.g., ViraMed and Euroimmun, Germany), all of which are Conformité Européenne (CE) marked and therefore meet regulatory standards for in vitro diagnostics in the European market. .. Published data show that these CE-marked IgM immunoblot assays (ViraMed, Euroimmun) demonstrate strong diagnostic accuracy, with reported sensitivities ranging from 90.0% to 94.4% and specificities between 97.1% and 99.2% when evaluated against composite or reference standards in infants and neonates with suspected CS ( , ).

Peptide ELISA:

Article Title: Evaluation of standard and modified two-tiered testing algorithms using well-characterized early Lyme disease samples
Article Snippet: .. Serologic testing was performed using (i) a VlsE/pepC10 IgM/IgG ELISA (Zeus Scientific, Raritan, NJ), followed by IgM and IgG ViraStripe immunoblots (Viramed; Biotech AG, Germany) at Mayo Clinic (MC, Rochester, MN); and (ii) a C6 peptide ELISA (Oxford Immunotec, Marlborough, MA) performed at Stony Brook University (SB, Stony Brook, NY). ..

Diagnostic Assay:

Article Title: Diagnostic potential for IgM antibody detection by the DPP Syphilis TnT assay in neonates at risk for congenital syphilis
Article Snippet: There are commercial IgM immunoblot and enzyme-linked immunosorbent assay (ELISA) assays used in Europe (e.g., ViraMed and Euroimmun, Germany), all of which are Conformité Européenne (CE) marked and therefore meet regulatory standards for in vitro diagnostics in the European market. .. Published data show that these CE-marked IgM immunoblot assays (ViraMed, Euroimmun) demonstrate strong diagnostic accuracy, with reported sensitivities ranging from 90.0% to 94.4% and specificities between 97.1% and 99.2% when evaluated against composite or reference standards in infants and neonates with suspected CS ( , ). .. In contrast, the CE-marked Euroimmun IgM ELISA typically shows more modest sensitivity (≈60%) despite specificity approaching 100%.

In Vitro:

Article Title: Diagnostic potential for IgM antibody detection by the DPP Syphilis TnT assay in neonates at risk for congenital syphilis
Article Snippet: .. There are commercial IgM immunoblot and enzyme-linked immunosorbent assay (ELISA) assays used in Europe (e.g., ViraMed and Euroimmun, Germany), all of which are Conformité Européenne (CE) marked and therefore meet regulatory standards for in vitro diagnostics in the European market. .. Published data show that these CE-marked IgM immunoblot assays (ViraMed, Euroimmun) demonstrate strong diagnostic accuracy, with reported sensitivities ranging from 90.0% to 94.4% and specificities between 97.1% and 99.2% when evaluated against composite or reference standards in infants and neonates with suspected CS ( , ).



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