Monkey β-CTx(Beta Crosslaps) ELISA Kit
SKU: E-EL-MK2116
Monkey β-CTx(Beta Crosslaps) ELISA Kit
Detection Range | 125.00-8000 pg/mL |
Sensitivity | 75.00 pg/mL |
Product Details
Properties
Assay type | Competitive-ELISA |
Format | 96T |
Assay time | 2.5h |
Detection range | 125.00-8000 pg/mL |
Sensitivity | 75.00 pg/mL |
Sample type &Sample volume | ; 50μL |
Specificity | This kit recognizes β-CTx in samples. No significant cross-reactivity or interference between β-CTx and analogues was observed. |
Reproducibility | Both intra-CV and inter-CV are < 10%. |
Application | This ELISA kit applies to the in vitro quantitative determination of β-CTx concentrations in . |
Test Principle
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with β-CTx. During the reaction, β-CTx in the sample or standard competes with a fixed amount of β-CTx on the solid phase supporter for sites on the Biotinylated Detection Ab specific to β-CTx. Excess conjugate and unbound sample or standard are washed away, and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns from blue to yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of β-CTx in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Kit Components and Storage
An unopened kit can be stored at 2-8℃ for 1 month. If the kit is not supposed to be used within 1 month, store the components separately according to the following conditions once the kit is received.
Item | Specifications | Storage |
---|---|---|
Micro ELISA Plate(Dismountable) | 96T: 8 wells ×12 strips 48T: 8 wells ×6 strips |
-20℃, 6 months |
Reference Standard | 96T: 2 vials 48T: 1 vial |
|
Concentrated Biotinylated Detection Ab (100×) | 96T: 1 vial, 120 μL 48T: 1 vial, 60 μL |
|
Concentrated HRP Conjugate (100×) | 96T: 1 vial, 120 μL 48T: 1 vial, 60 μL |
-20℃(Protect from light), 6 months |
Reference Standard & Sample Diluent | 1 vial, 20 mL | 2-8°C, 6 months |
Biotinylated Detection Ab Diluent | 1 vial, 14 mL | |
HRP Conjugate Diluent | 1 vial, 14 mL | |
Concentrated Wash Buffer (25×) | 1 vial, 30 mL | |
Substrate Reagent | 1 vial, 10 mL | 2-8℃(Protect from light) |
Stop Solution | 1 vial, 10 mL | 2-8℃ |
Plate Sealer | 5 pieces | |
Manual | 1 copy | |
Certificate of Analysis | 1 copy |
Technical Data:
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level β-CTx were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level β-CTx were tested on 3 different plates, 20 replicates in each plate.
Intra-assay Precision | Inter-assay Precision | |||||
---|---|---|---|---|---|---|
Sample | 1 | 2 | 3 | 1 | 2 | 3 |
n | 20 | 20 | 20 | 20 | 20 | 20 |
Mean (pg/mL) | 441.29 | 936.13 | 2891.85 | 477.86 | 968.26 | 2650.94 |
Standard deviation | 23.12 | 37.73 | 155.58 | 31.83 | 54.61 | 139.17 |
CV (%) | 5.24 | 4.03 | 5.38 | 6.66 | 5.64 | 5.25 |
Recovery
The recovery of β-CTx spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.
Sample Type | Range (%) | Average Recovery (%) |
---|---|---|
Serum(n=8) | 91-103 | 96 |
EDTA plasma(n=8) | 92-108 | 100 |
Cell culture media(n=8) | 93-109 | 100 |
Target Information
Database Links | SwissProt: F7BJV7(1207-1214aa) |
Synonyms | b-CTx;bCTXI;bCTX-I;B-Cr;BCL;Type I Collagen C-Telopeptide-Related Fraction |
Research Area | Signal transduction,Metabolism |
Assay Procedures
1. Add 50μL standard or sample to the wells, immediately add 50μL Biotinylated Detection Ab working solution to each well. Incubate for 45 min at 37°C |
|
2. Aspirate and wash the plate for 3 times |
|
3. Add 100μL HRP conjugate working solution. Incubate for 30 min at 37°C. Aspirate and wash the plate for 5 times |
|
4. Add 90μL Substrate Reagent. Incubate for 15 min at 37°C |
|
5. Add 50μL Stop Solution |
|
6. Read the plate at 450nm immediately. Calculation of the results |