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| Company | IBL-America | IBL-America | IBL-America | IBL-America | IBL-America |
| Item | Chlamydia IgG (Pneumonia) ELISA | Adenovirus IgG ELISA | Anti-Cetuximab (Erbitux®) ELISA | Complement System Classical Pathway ELISA Assay | IGF-1 ELISA Assay |
| Catalog Number | IB19216 | IB79844 | TM09027 | COMPL CP310 RUO | E20 |
| Price | Supplier Page | Supplier Page | Supplier Page | Supplier Page | Supplier Page |
| Description | Enzyme linked immunosorbent assay (ELISA) for the determination of IgG antibody to C. Pneumoniae in human serum or plasma. For research use only, not for use in diagnostic procedures. | The Adenovirus IgG ELISA is intended for the qualitative determination of IgG class antibodies against Adenovirus in human serum or plasma (citrate, heparin). 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 Wieslab® COMPL CP310 is an enzyme immunoassay (ELISA) for the determination of functional classical complement pathway in human serum. For research use only, not for use in diagnostic procedures. | Enzyme immunoassay (ELISA) for the determination of levels of IGF-I in serum or plasma. For research use only, not for use in diagnostic procedures. |
| Detection Target | Chlamydia IgG (Pneumonia) | Adenovirus IgG | sAPP Alpha | Human Phopsho Tau (217P) | Alpha-Klotho (Soluble) |
| Sample Type | Human serum or plasma. | Serum, Blood Plasma | Serum, Blood Plasma, CSF, Cell Culture Supernatant | Cerebrospinal fluids | Serum, plasma (EDTA, Heparin, Citrate), urine 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 | 1 calibrator used to calculate Antibody Index value (see 'Results' section of protocol). | A cut-off control is used for the interpretation of results. | 0 / 1 - 30 ng/mL | Inquire | 2 to 50 ng/mL |
| Sensitivity | Inquire | 100% (95% confidence interval: 95.2% - 100%) | 0.09 ng/mL | 8.07 pg/mL | 6.15 pg/mL |
| Assay Time | 20 min. incubation (RT) + 20 min. (RT) + 10 min. = 50 min. total incubation time. | 1 hr 45 mins (incubation) | 2 hours, 15 min. total incubation time. | 2 hrs (incubation) | 1 hr 45 mins (incubation) |
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