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| Company | IBL-America | IBL-America | IBL-America | IBL-America | IBL-America |
| Item | Chlamydia IgG (Trachomatis) ELISA | Bordetella pertussis IgM ELISA | CMV IgG ELISA Assay | Coxiella burnetii (Q-Fever) Phase 1 IgG ELISA Assay | Treponema pallidum (Syphilis) IgG ELISA Assay |
| Citations | | | | | |
| Catalog Number | IB19202 | IB79851 | IB19205 | IB79833 | IB79832 |
| Price | Supplier Page | Supplier Page | Supplier Page | Supplier Page | Supplier Page |
| Description | Enzyme linked immunosorbent assay (ELISA) for the detection of IgG antibody to Chlamydia Trachomatis in human serum or plasma. For research use only, not for use in diagnostic procedures. | The Bordetella pertussis IgM ELISA is intended for the determination of IgM class antibodies against Bordetella pertussis in human serum or plasma (citrate, heparin). For research use only - not for use in diagnostic procedures. | Enzyme linked immunosorbent assay (ELISA) for the determination of IgG antibody to Cytomegalovirus (CMV) in human serum or plasma. For research use only, not for use in diagnostic procedures. | Enzyme immunoassay (ELISA) for the determination of IgG class antibodies against Coxiella burnetii phase 1 in the early stages of infection in human serum. For research use only, not for use in diagnostic procedures. | Enzyme-linked immunosorbent assay (ELISA) for the determination of IgG-class antibodies to Treponema pallidum in serum. For research use only, not for use in diagnostic procedures. |
| Detection Target | Chlamydia IgG (Trachomatis) | Serotonin | Deamidated Gliadin IgG | Coxiella burnetii (Q-Fever) Phase 1 IgG | Estriol |
| Sample Type | Human serum or plasma. | Multiple | Serum | Serum | Serum |
| Method | Enzyme-Linked Immunosorbent Assay (ELISA) | Enzyme-Linked Immunosorbent Assay (ELISA) | Enzyme-Linked Immunosorbent Assay (ELISA) | Enzyme-Linked Immunosorbent Assay (ELISA) | Enzyme-Linked Immunosorbent Assay (ELISA) |
| Detection Range | Cut-off value (calculated from the OD of the calibrator) used to interpret results of unknowns. | A cut-off control is used for the interpretation of results. | Inquire | Inquire | Inquire |
| Sensitivity | Inquire | 0.005 ng/mL x Correction Factor based upon volume of sample used. | 0.706 | 88% | 0.075 ng/mL |
| Assay Time | 20 min.incubation (RT) + 20 min. (RT) + 10 min. (RT) + 50 min. total incubation time. | 1 hr 45 mins (incubation) | 50 mins (incubation) | 1 hr 45 mins (incubation) | 1 hr 45 mins (incubation) |
| Get Quote | Supplier Page | Supplier Page | Supplier Page | Supplier Page | Supplier Page |