|  |  |  |  |  |
| Company | IBL-America | IBL-America | IBL-America | IBL-America | IBL-America |
| Item | Strongyloides IgG / IgM ELISA | Angiotensinogen Total ELISA Assay | Epstein-Barr Virus (EBNA-1) IgM ELISA | sAPPß-sw (highly sensitive) ELISA Assay | Varicella-Zoster Virus (VZV) IgG ELISA |
| Citations | | | | | |
| Catalog Number | IB79344 | 27412 | IB79860 | 27733 | IB79889 |
| Price | Supplier Page | Supplier Page | Supplier Page | Supplier Page | Supplier Page |
| Description | The Strongyloides ELISA test is an enzyme immunoassay for the detection of antibodies to Strongyloides, in human serum or plasma (citrate or heparin). For research use only, not for use in diagnostic procedures. | Solid phase sandwich ELISA for the determination of human Angiotensinogen ELISA in serum, EDTA-plasma, urine, or cell culture media. For research use only, not for use in diagnostic procedures. | Enzyme immunoassay for the determination of IgM-class antibodies to Epstein-Barr virus nuclear-1 antigen (EBV-EBNA-1) in human serum or plasma. For research use only - not for use in diagnostic procedures. | Solid phase sandwich ELISA for the determination human sAPP_x0001_-sw in EDTA plasma of the Tg2576 transgenic mouse and cell culture supernatant. For research use only, not for use in diagnostic procedures. | The Varicella-Zoster Virus (VZV) IgG ELISA is intended for the determination of IgG class antibodies against Varicella-Zoster Virus (VZV) in human serum or plasma (citrate, heparin). For research use only - not for use in diagnostic procedures. |
| Detection Target | T3 (Free) | Anti-Bevacizumab (Avastin®) | Schistosoma mansoni IgG | Histamine | Strongyloides IgG / IgM |
| Sample Type | Serum | Serum and plasma. | Serum, Blood Plasma | Multiple | Serum, Blood Plasma |
| 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. | 0.31 to 20.00 ng/mL | A cut-off control is used for the interpretation of results. | 0.39 to 25.00 ng/mL | A cut-off control is used for the interpretation of results. |
| Sensitivity | Inquire | 40 ng/mL | 93.75% (95% confidence interval: 82.8% - 98.69%) | 0.2 ng/mL | 0.879 |
| Assay Time | 1 hr 45 mins (incubation) | 2 hrs (incubation) | 1 hr 45 mins (incubation) | Overnight + 1 hr (incubation) | 1 hr 45 mins (incubation) |
| Get Quote | Supplier Page | Supplier Page | Supplier Page | Supplier Page | Supplier Page |