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Chembio Diagnostics chagas stat pak
Serological and molecular characterization of plasma samples. Individual plasma samples reactivity with Wiener Chagatest ELISA ( A ), Hemagen <t>Chagas</t> ELISA ( B ) and parasite burden measured by qPCR ( C ). Samples were classified as negative (Neg), positive (Pos), or discordant (Disc) based on serological and molecular assays and are color-coded based on country of origin. There was no significant difference in parasite burden between positive and discordant samples ( t = 1.09; P = 0.29). The dotted line in A and B indicates the cut-off for reactive samples
Chagas Stat Pak, supplied by Chembio Diagnostics, 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/chagas+stat+pak/pmc13197337-79-6-10?v=Chembio+Diagnostics
Average 86 stars, based on 1 article reviews
chagas stat pak - by Bioz Stars, 2026-07
86/100 stars

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1) Product Images from "Epitope mapping and conservation of antigens from the Multi-Cruzi immunoassay platform"

Article Title: Epitope mapping and conservation of antigens from the Multi-Cruzi immunoassay platform

Journal: Medical Microbiology and Immunology

doi: 10.1007/s00430-026-00877-z

Serological and molecular characterization of plasma samples. Individual plasma samples reactivity with Wiener Chagatest ELISA ( A ), Hemagen Chagas ELISA ( B ) and parasite burden measured by qPCR ( C ). Samples were classified as negative (Neg), positive (Pos), or discordant (Disc) based on serological and molecular assays and are color-coded based on country of origin. There was no significant difference in parasite burden between positive and discordant samples ( t = 1.09; P = 0.29). The dotted line in A and B indicates the cut-off for reactive samples
Figure Legend Snippet: Serological and molecular characterization of plasma samples. Individual plasma samples reactivity with Wiener Chagatest ELISA ( A ), Hemagen Chagas ELISA ( B ) and parasite burden measured by qPCR ( C ). Samples were classified as negative (Neg), positive (Pos), or discordant (Disc) based on serological and molecular assays and are color-coded based on country of origin. There was no significant difference in parasite burden between positive and discordant samples ( t = 1.09; P = 0.29). The dotted line in A and B indicates the cut-off for reactive samples

Techniques Used: Clinical Proteomics, Enzyme-linked Immunosorbent Assay



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Serological and molecular characterization of plasma samples. Individual plasma samples reactivity with Wiener Chagatest ELISA ( A ), Hemagen Chagas ELISA ( B ) and parasite burden measured by qPCR ( C ). Samples were classified as negative (Neg), positive (Pos), or discordant (Disc) based on serological and molecular assays and are color-coded based on country of origin. There was no significant difference in parasite burden between positive and discordant samples ( t = 1.09; P = 0.29). The dotted line in A and B indicates the cut-off for reactive samples

Journal: Medical Microbiology and Immunology

Article Title: Epitope mapping and conservation of antigens from the Multi-Cruzi immunoassay platform

doi: 10.1007/s00430-026-00877-z

Figure Lengend Snippet: Serological and molecular characterization of plasma samples. Individual plasma samples reactivity with Wiener Chagatest ELISA ( A ), Hemagen Chagas ELISA ( B ) and parasite burden measured by qPCR ( C ). Samples were classified as negative (Neg), positive (Pos), or discordant (Disc) based on serological and molecular assays and are color-coded based on country of origin. There was no significant difference in parasite burden between positive and discordant samples ( t = 1.09; P = 0.29). The dotted line in A and B indicates the cut-off for reactive samples

Article Snippet: These samples had been tested with Chagas STAT PAK ® (Chembio Diagnostic, Inc.), Trypanosoma DetectTM (InBios), Chagatest ELISA recombinant v.3.0 (Wiener), and Hemagen ® Chagas’ Kit (Hemagen) as well as by quantitative real time PCR and two end-point PCR assays, one targeting nuclear satellite DNA (primers TcZ1-TcZ2) [ ], and one targeting minicircle DNA (primers 121–122) [ ], with extensive quality control and cross-validation among participating laboratories [ , ].

Techniques: Clinical Proteomics, Enzyme-linked Immunosorbent Assay