| Field | Specification |
|---|---|
| Assay Time | |
| Detection Method | |
| Detection Range | |
| Product Type | |
| Reactivity | |
| Sample Type(s) | Serum, Plasma, Other Biological Fluids |
| Sensitivity | |
| Storage |
Assay Principle
This Human IL17 CLIA Kit employs a solid-phase chemiluminescent immunoassay for quantitative determination of Interleukin 17 in Serum, Plasma, Other Biological Fluids. Capture antibodies pre-coated in microplate wells bind the target analyte. Following incubation and wash steps, an HRP-conjugated detection antibody is applied. A chemiluminescent substrate generates a light signal read by luminometer and analyte concentration is interpolated from a standard curve.
Scientific Background
Cytokines and chemokines are secreted signaling proteins that coordinate immune cell recruitment, activation, and inflammatory responses. These pleiotropic mediators act through cognate receptors on target cells, activating JAK-STAT, NF-κB, and MAPK pathways. Dysregulated cytokine expression underlies autoimmune, infectious, and inflammatory pathologies.
Kit Performance Data
| Detection Range | 12.5~800pg/mL |
|---|---|
| Sensitivity (LLOQ) | 7.5pg/mL |
| Detection Method | Chemiluminescence |
| Assay Duration | 3.5 hours |
| Compatible Sample Types | Serum, Plasma, Other Biological Fluids |
| Species Reactivity | Human |
Specificity
This kit recognizes Human IL-17 in samples. No significant cross-reactivity or interference between Human IL-17 and analogues was observed.
Safety & Handling
For Research Use Only (RUO). Not intended for diagnostic use. Handle all biological samples as potentially infectious per institutional biosafety protocols. Review the Safety Data Sheet (SDS) before use.
This Human IL17 CLIA Kit has been validated for use with Serum, Plasma, Other Biological Fluids. Samples should be freshly collected, properly anticoagulated where applicable, and clarified by centrifugation before assay. Avoid repeated freeze-thaw cycles. Non-validated sample types may require independent validation before results can be interpreted with confidence.
The sensitivity (lowest limit of quantification, LLOQ) is 7.5pg/mL. Samples expected to contain concentrations below this value should be considered below the limit of detection (BLD) and reported accordingly. Measurements near the LLOQ may show increased variability and should be interpreted cautiously or confirmed by replicate analysis.
The total assay duration is approximately 3.5 hours, including all incubation, wash, and detection steps. This estimate does not include sample preparation time. Ensure luminometer availability in advance and allow all kit reagents to equilibrate to the recommended assay temperature before starting.
This kit uses chemiluminescent detection and requires a luminometer — or a multimode plate reader with luminescence capability — that can read standard 96-well microplates. Conventional absorbance-based plate readers are not compatible with this assay format. Calibrate your instrument according to the manufacturer's specifications before use.
No. This kit is strictly for Research Use Only (RUO) and is not intended, validated, or approved for clinical diagnostic applications. Results must not be used to guide patient management or clinical decisions. For in vitro diagnostic purposes, use only CE-marked or FDA-cleared assays validated for the intended clinical use.
BioHippo partners with leading life science suppliers to offer flexible purchasing and support options. Contact our team to discuss the following add-on services.
- Bulk & Volume Pricing: Reduced per-unit pricing for multi-unit or project-scale orders. Submit a quote request for a customized offer.
- Expedited Fulfillment: Priority order handling may be available for time-sensitive projects. Confirm availability before ordering.
- Technical Consultation: Our scientific team provides protocol guidance and troubleshooting at no additional charge.
- Custom Configurations: Alternative formulations, pack sizes, or kit configurations may be available upon request.
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