Shikari® (S-ATG) Anti-Golimumab ELISA
GOL-QLS-SIM
Enzyme immunoassay for the qualitative determination of specific antibodies to Golimumab (Simponi®) in human serum and plasma.
This kit has been especially developed for the qualitative determination of golimumab in serum and plasma samples.
This kit has been especially developed for the qualitative determination of golimumab in serum and plasma samples.
The Matriks Biotek Antibody to Golimumab ELISA Kit can be efficiently used for monitoring anti-Golimumab antibodies during therapy and offers the clinician a tool for decision on possible preventive measures such as possible addition of immunosuppressive drug to reduce anti-Golimumab antibodies. Measurement of biological drug trough levels and antibody to biological drug gained high importance during the course of treatment. These measurements enable dose adjustments and switch to another class of biological drug when necessary.
All SHIKARI® ELISA kits are suitable for biosimilar work.
All SHIKARI® ELISA kits are produced under ISO 13485 quality system and have CE IVD mark.
For technical inquiry, IFU and other relevant documents please contact techsupport@matriksbiotek.com
| Required Volume (µl) | 20 |
| Total Time (min) | 140 |
| Sample | Serum, plasma |
| Sample Number | 96 |
| Detection Limit (ng/mL) | +/- |
| Spike Recovery (%) | - |
| Shelf Life (year) | 1 |
| Assay type | Qualitative |
| Species Reactivity | Human |
| Storage conditions | Store at +4°C. Please refer to protocols. |
| Shipping conditions | At room temperature |
| # | File | Action |
|---|---|---|
| Safety Data Sheet (SDS) | Download |
Publications with this drug
| # | File | Action |
|---|---|---|
| Tawa, Hideki, et al. "Therapeutic drug monitoring of golimumab for the prediction of long-term clinical remission in patients with ulcerative colitis." Digestion 103.5 (2022): 329-338. | Visit Link |
