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| Company | IBL-America | IBL-America | IBL-America | IBL-America | IBL-America |
| Item | Parvovirus B19 IgG ELISA | Androstenedione ELISA Assay | Anti-Cetuximab (Erbitux®) ELISA | Bordetella pertussis IgM ELISA | Deamidated Gliadin IgG ELISA Assay |
| Catalog Number | IB05001 | IB79119 | TM09027 | IB79851 | KAPDTDGLG02 |
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| Description | Enzyme immunoassay (ELISA) for the determination of human IgG antibodies directed against Parvovirus B19 in serum or plasma (EDTA, citrate, heparin). For research use only, not for use in diagnostic procedures. | Solid phase competitive enzyme-linked immunosorbent assay (ELISA) for the determination of Androstenedione in serum and EDTA plasma. FDA exempt, can be used for in-vitro diagnostics. | Enzyme immunoassay (ELISA) test kit for the determination of free antibodies directed against the drug Cetuximab (Erbitux®) in serum and 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. | Solid phase enzyme immunoassay (ELISA) for the detection of IgG antibodies to deamidated gliadin in human serum. For research use only, not for use in diagnostic procedures. |
| Detection Target | Parvovirus B19 IgG | 1,3,5(10)-estratriene-3,17ß-diol; 17ß-estradiol; E2. | sAPP Alpha | Serotonin | Intact Proinsulin |
| Sample Type | Serum or plasma (EDTA, citrate, heparin). | Human serum or plasma (EDTA, lithium heparin, or citrate plasma). | Serum, Blood Plasma, CSF, Cell Culture Supernatant | Multiple | Serum, EDTA-plasma, and cell culture supernatant. |
| 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 | A calculated cut-off value is used to interpret results of unknowns. | 0.1 to 10.0 ng/mL | 0 / 1 - 30 ng/mL | A cut-off control is used for the interpretation of results. | 25 to 400 U/mL |
| Sensitivity | >99% | 10.6 pg/mL | 0.09 ng/mL | 0.005 ng/mL x Correction Factor based upon volume of sample used. | 6.83 pg/mL |
| Assay Time | 1 hour (37°C) + 30 min. (37°C) + 30 min. (37°C) = 2 hours total incubation time. | 1 hr 30 mins (incubation) | 2 hours, 15 min. total incubation time. | 1 hr 45 mins (incubation) | 1 hr 10 mins (incubation) |
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