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A. cantonensis infection was diagnosed by immunoblot testing at the Department of Helminthology, Faculty of Tropical Medicine, Mahidol University, Bangkok.
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The antibody specificity was preliminarily assayed by immunoblot tests.
Similarly, samples in the HCV seroconversion panel, which showed early detection as tested using the Hi3-1 asuggestedgesthe the result of isolated reactivity for anti-Core by immunoblot test.
The serological response was monitored by immunoblotting test and with both P48- and TA- ELISA kits.
Diagnosis for 6 of these patients was confirmed by using immunoblot tests (Dengue IgM Blot and Dengue IgG Blot, Genelabs Diagnostics, Singapore).
Sensitivity and specificity of A116k mAb was evaluated on immunoblot by testing following controls.
All had been previously diagnosed using an anti-HIV antibody screening test (Vironostika, Organon Tednika, The Netherlands) which was confirmed by immunoblot-based testing (Gene Lab Diagnostics, Singapore).
Antibody to P. insidiosum was detected in a serum sample by immunoblot and immunochromatography tests (ICT).
Cas9 expression was tested by immunoblot using 4 12% Bis-Tris SDS polyacrylamide gels (used for all immunoblot applications in this work).
When tested by immunoblot analysis, sera from AncC and ConC env immunized guinea pigs recognized a greater number of primary subtype C envelope glycoproteins than sera from guinea pigs immunized with a contemporary subtype C env control.
Betaglycan transfection efficiency was tested by immunoblot using monoclonal anti-c-myc antibody.
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