Monkey OC/BGP(Osteocalcin) ELISA Kit
Item No:
E-EL-MK1801c
Chinese Name:
Alias:
BGLAP, BGP, OC, OCN, bone gamma-carboxyglutamate protein, Osteocalcin
Keywords:
Classification:
Retail Price
¥ 3500
Market Price
¥ 3500
-
Spec
- 48T
- 96T
- 96T*5
Inventory surplus
2997
隐藏域元素占位
- Product Comparison
Describe
Use
This kit is used for the in vitro quantification of OC/BGP in Monkey serum, plasma or other biological fluids
Detection principle
This kit adopts double antibody sandwich ELISA method. Anti-Monkey OC/BGP antibody is used to coat the ELISA plate. Monkey OC/BGP in the sample or standard will bind to the coating antibody during the experiment, and the free components are washed away. Biotinylated anti-monkey OC/BGP antibody and horseradish peroxidase-labeled affinity are added sequentially. The anti-monkey OC/BGP antibody binds to the monkey OC/BGP bound to the encapsulated antibody, and the biotin binds specifically to the affin to form an immune complex, and the free components are washed away. The chromogenic substrate (TMB) was added, and TMB appeared blue catalyzed by horseradish peroxidase and turned yellow after the addition of termination solution. The concentration of OC/BGP in the sample was calculated by plotting the standard curve.
| Reaction Type | Sandwich method |
| Specification | 96T |
| Reaction time | 3.5h |
| Reactivity | Monkey |
| Detection method | Colormetric |
| Detection range | 0.78—50 ng/mL |
| Sensitivity | 0.47 ng/mL |
| Sample volume | 100μL |
| Sample type | Serum, plasma or other biological fluids |
Specificity
It can detect monkey OC/BGP in the sample without significant cross-reactivity with other related proteins.
Repeatability
Within the plates, the coefficients of variation between the plates were <10%.
Typical Data
The OD values of the standard curves may vary due to different experimental operating conditions (e.g. operator, pipetting technique, plate washing technique and stabilization conditions, etc.). The following data and curves are for reference only. Experimenters need to establish standard curves according to their own experiments.
| (ng/mL) | O.D | Average | Corrected |
|---|---|---|---|
| 50 | 2.435 2.477 |
2.456 | 2.39 |
| 25 | 1.705 1.719 |
1.712 | 1.646 |
| 12.5 | 0.953 0.935 |
0.944 | 0.878 |
| 6.25 | 0.424 0.458 |
0.441 | 0.375 |
| 3.13 | 0.294 0.27 |
0.282 | 0.216 |
| 1.57 | 0.171 0.169 |
0.17 | 0.104 |
| 0.78 | 0.112 0.126 |
0.119 | 0.053 |
| 0 | 0.058 0.074 |
0.066 | -- |

Precision
Intra-plate precision: 20 times on 1 plate for low, medium and high concentration samples.
Intra-plate precision: 20 times on 3 plates for low, medium and high concentrations.
| Intra-assay Precision | Inter-assay Precision | |||||
|---|---|---|---|---|---|---|
| Sample | 1 | 2 | 3 | 1 | 2 | 3 |
| n | 20 | 20 | 20 | 20 | 20 | 20 |
| Mean (ng/mL) |
2.70 | 6.48 | 21.99 | 2.85 | 7.09 | 22.11 |
| Standard deviation |
0.14 | 0.30 | 0.93 | 0.15 | 0.34 | 0.82 |
| C V (%) | 5.19 | 4.63 | 4.23 | 5.26 | 4.80 | 3.71 |
Recovery rate
Recovery experiments were performed by adding known concentrations of the target protein to five different samples, and the recovery range and average recovery were obtained.
| Sample Type | Range (%) | Average Recovery (%) |
|---|---|---|
| Serum (n=8) | 95-106 | 100 |
| EDTA plasma (n=8) | 97-112 | 102 |
| Cell culture media (n=8) | 86-100 | 92 |
Linearity
Five samples were spiked with known concentrations of target proteins, and the recovery experiments were performed to obtain the range of recovery rates and average recovery rates. Five samples were diluted 2, 4, 8 and 16 times for recovery experiments, and the range of recovery rates and average recovery rates were obtained.
| Serum (n=5) | EDTA plasma (n=5) | Cell culture media (n=5) | ||
|---|---|---|---|---|
| 1:2 | Range (%) | 86-100 | 86-96 | 95-109 |
| Average (%) | 91 | 91 | 101 | |
| 1:4 | Range (%) | 93-107 | 80-89 | 89-101 |
| Average (%) | 99 | 85 | 94 | |
| 1:8 | Range (%) | 93-104 | 82-96 | 87-100 |
| Average (%) | 98 | 87 | 93 | |
| 1:16 | Range (%) | 92-108 | 83-98 | 86-101 |
| Average (%) | 99 | 90 | 92 |
Reagent kit composition and storage
Unopened kits can be stored at 2-8°C for one week; if the kit is used after one week, please unpack the kit and store each component separately according to the conditions in the table below.
| Chinese name | English Name | Specification | Storage conditions |
|---|---|---|---|
| ELISA enzyme standard plate (detachable) | Micro ELISA Plate(Dismountable) | 8 holes×12 strips | -20℃, can be stored for 6 months |
| Lyophilized standards | Reference Standard | 2 sticks | |
| Concentrated biotinylated antibody(100×) | Concentrated Biotinylated Detection Ab | 1 x 120 μL | |
| Concentrated HRP enzyme conjugate(100×) | Concentrated HRP Conjugate | 1 x 120 μL | -20℃(keep away from light), can be stored for 6 months |
| Standard & Sample Diluent | Reference Standard & Sample Diluent | 1 bottle of 20 mL | 2-8℃. Can be stored for 6 months |
| Biotinylated antibody diluent | Biotinylated Detection Ab Diluent | 1 bottle 14 mL | |
| Enzyme Conjugate Diluent | HRP Conjugate Diluent | 1 bottle 14 mL | |
| Concentrated Washing Solution(25×) | Concentrated Wash Buffer (25×) | 1 bottle 30 mL | |
| Substrate solution (TMB) | Substrate Reagent | 1 bottle 10 mL | 2-8℃(keep away from light) |
| Reaction termination solution | Stop Solution | 1 bottle 10 mL | 2-8℃ |
| Plate lamination | Plate Sealer | 5 sheets | |
| Product manual | Product Description | 1 copy | |
| Quality inspection report | Certificate of Analysis | 1 copy |
Note: All reagent bottles must be tightly capped to prevent evaporation and microbial contamination.
The volume of reagents is subject to the actual shipping instructions. The relevant reagents will be slightly more than the volume indicated on the label when dispensing, please measure rather than pour directly when using.
Self-provided items required for the test
1. ELISA (450 nm wavelength filter)
2. High-precision pipettes, EP tubes and disposable tips: 0.5-10 μL, 2-20 μL, 20-200 μL, 200-1000 μL
3. 37°C thermostat, double-distilled water or deionized water
4. absorbent paper
操作步骤
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1. Add 100 μL of standard working solution or sample to the corresponding plate wells and incubate at 37°C for 90 minutes |
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2. After discarding the liquid in the plate, add 100 μL of biotinylated antibody working solution and incubate at 37°C for 60 minutes. |
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3. Discard the liquid in the plate and wash the plate 3 times |
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4. Add 100μL of HRP enzyme conjugate working solution to each well, incubate at 37℃ for 30 minutes, discard the liquid in the plate, and wash the plate 5 times |
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5. Add 90μL of substrate solution to each well and incubate at 37℃ for 15 minutes |
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6. Add 50μL of termination solution to each well |
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7. Read immediately at 450 nm and process the data |
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