TNF-related apoptosis-inducing ligand (TRAIL), also known as Apo-2 ligand and TNFSF10, is a type II transmembrane protein with a carboxy-terminal extracellular domain that exhibits homology to other TNF superfamily members. Among TNF superfamily members, TRAIL is the most homologous to Fas Ligand, sharing 28% amino acid sequence identity in their extracellular domains. Human TRAIL shares 65% amino acid sequence identity with mouse TRAIL and is active on mouse cells.
Human TRAIL/TNFSF10 Quantikine ELISA Kit
R&D Systems | Catalog # DTRL00
Key Product Details
Assay Length
Sample Type & Volume Required Per Well
Sensitivity
Assay Range
Product Summary for Human TRAIL/TNFSF10 Quantikine ELISA Kit
Product Specifications
Assay Type
Format
Measurement
Detection Method
Conjugate
Species
Specificity
Cross-reactivity
Interference
精度
Intra-Assay Precision (Precision within an assay) Three samples of known concentration were tested on one plate to assess intra-assay precision.
Inter-Assay Precision (Precision between assays) Three samples of known concentration were tested in separate assays to assess inter-assay precision.
Cell Culture Supernates, Cell Lysates, Saliva
| Intra-Assay Precision | Inter-Assay Precision | |||||
|---|---|---|---|---|---|---|
| Sample | 1 | 2 | 3 | 1 | 2 | 3 |
| n | 20 | 20 | 20 | 40 | 40 | 40 |
| Mean (pg/mL) | 95.0 | 193 | 391 | 96.0 | 191 | 388 |
| Standard Deviation | 4.26 | 8.81 | 24.3 | 8.30 | 14.8 | 22.2 |
| CV% | 4.5 | 4.6 | 6.2 | 8.6 | 7.7 | 5.7 |
EDTA Plasma, Heparin Plasma, Serum
| Intra-Assay Precision | Inter-Assay Precision | |||||
|---|---|---|---|---|---|---|
| Sample | 1 | 2 | 3 | 1 | 2 | 3 |
| n | 20 | 20 | 20 | 40 | 40 | 40 |
| Mean (pg/mL) | 102 | 203 | 408 | 102 | 202 | 407 |
| Standard Deviation | 3.45 | 5.73 | 23.0 | 7.59 | 12.2 | 17.8 |
| CV% | 3.4 | 2.8 | 5.6 | 7.5 | 6.1 | 4.4 |
Recovery for Human TRAIL/TNFSF10 Quantikine ELISA Kit
The recovery of TRAIL spiked to levels throughout the range of the assay in various matrices was evaluated.
| Sample Type | Average % Recovery | Range % |
|---|---|---|
| Cell Culture Media (n=4) | 101 | 92-105 |
| EDTA Plasma (n=4) | 103 | 96-112 |
| Heparin Plasma (n=4) | 103 | 98-115 |
| Serum (n=4) | 96 | 91-102 |
Linearity
To assess the linearity of the assay, samples containing or spiked with high concentrations of TRAIL were serially diluted with the appropriate Calibrator Diluent to produce samples with values within the dynamic range of the assay.
Scientific Data Images for Human TRAIL/TNFSF10 Quantikine ELISA Kit
Human TRAIL/TNFSF10 ELISA Cell Culture Supernate/Cell Lysate/Saliva Standard Curve
Human TRAIL/TNFSF10 ELISA Serum/Plasma Standard Curve
Preparation and Storage
Shipping
Stability & Storage
Background: TRAIL/TNFSF10
Long Name
Alternate Names
Gene Symbol
Additional TRAIL/TNFSF10 Products
Product Documents for Human TRAIL/TNFSF10 Quantikine ELISA Kit
Product Specific Notices for Human TRAIL/TNFSF10 Quantikine ELISA Kit
For research use only
⚠ WARNING: This product can expose you to chemicals including N,N-Dimethylforamide, which is known to the State of California to cause cancer. For more information, go to www.P65Warnings.ca.gov.Citations for Human TRAIL/TNFSF10 Quantikine ELISA Kit
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Sample Tested: SerumVerified Customer | Posted 11/15/2022
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Sample Tested: Cell Culture SupernatesVerified Customer | Posted 10/04/2017
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Protocols
View specific protocols for Human TRAIL/TNFSF10 Quantikine ELISA Kit (DTRL00):
- Prepare all reagents, standard dilutions, and samples as directed in the product insert.
- Remove excess microplate strips from the plate frame, return them to the foil pouch containing the desiccant pack, and reseal.
- Add 100 µL of Assay Diluent to each well.
- Add 50 µL of Standard, control, or sample to each well. Cover with a plate sealer, and incubate at room temperature for 2 hours on a horizontal orbital microplate shaker.
- Aspirate each well and wash, repeating the process 3 times for a total of 4 washes.
- Add 200 µL of Conjugate to each well. Cover with a new plate sealer, and incubate at room temperature for 2 hours on the shaker.
- Aspirate and wash 4 times.
- Add 200 µL Substrate Solution to each well. Incubate at room temperature for 30 minutes on the benchtop. PROTECT FROM LIGHT.
- Add 50 µL of Stop Solution to each well. Read at 450 nm within 30 minutes. Set wavelength correction to 540 nm or 570 nm.





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