VD(Vitamin D) ELISA Kit (E-EL-0012)
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For research use only.
Product Summary
| Sensitivity | 3.75 ng/mL |
| Detection Range | 6.25-400 ng/mL |
| Sample Volume | 50 μL |
| Total Assay Time | 2 h 30 min |
| Reactivity | Universal |
| Specificity | This kit recognizes Universal VD in samples.No significant cross-reactivity or interference between Universal VD and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, plasma and other biological fluids |
| Detection Method | Colorimetric method, ELISA, Competitive |
| Assay Type | Competitive-ELISA |
| Size | 96T / 48T / 24T / 96T*5 / 96T*10 |
| Storage | 2-8℃ |
| Expiration Date | 12 months |
Performance
| Typical data |
The following data was generated by the Quality Control Department, under controlled laboratory conditions (ambient temperature: 18-25 °C, relative humidity: 35-75%) using standardized procedures (TMB reaction at 37 °C in the dark for 15 minutes, followed by termination and OD measurement). These values are provided for reference only.
Actual results may vary due to differences in laboratory conditions, operator technique, and equipment. Users are required to generate a standard curve using their own experimental data.
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| Precision |
Intra-assay Precision (Within-run Precision): Three samples representing low, mid, and high concentrations of Human IL-6 were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Human IL-6 were tested on three separate plates, with 20 replicates per plate, to assess variability among assays.
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| Recovery |
The recovery of Universal VD was evaluated by spiking samples at low, mid, and high concentrations across the assay range in various sample matrices.
The assay performance was assessed by comparing the measured concentrations to the expected spiked amounts to determine the percent recovery.
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| Linearity |
Linearity of the assay was evaluated by spiking samples with high concentrations of Universal VD and performing serial dilutions using Standard & Sample Diluent to produce concentrations spanning the assay's dynamic range.
The measured values were then compared to the expected concentrations to assess the linearity of response.
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| Stability |
Each kit batch is subjected to accelerated stability testing and real-time stability monitoring. Sample performance is evaluated after storage at 37 °C for 10 days to assess the impact of elevated temperature on assay reliability and reagent integrity.
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Test Principle
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with Universal VD. During the reaction, Universal VD in the sample or standard competes with a fixed amount of Universal VD on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Universal VD. 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 Universal VD in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Background
Vitamin D is a fat-soluble vitamin made mainly from 7-dehydrocholesterol in the human body and ergosterol in plants or yeast by ultraviolet irradiation. Like vitamins A, E, and K, it is a fat-soluble vitamin that dissolves in fat and is best absorbed when taken at the same time as some fats. Vitamin D deficiency is common around the world and causes the body to absorb less calcium and phosphate to maintain healthy bones.
The way the body supplements vitamin D is mainly through sun exposure and diet. Sun exposure can ensure the synthesis of vitamin D within the body, which can significantly treat the improvement of calcium deficiency caused by insufficient vitamin D. Therefore, as for the "vitamin D" mentioned in the question, according to the information I have searched, it can be concluded that vitamin D is a fat-soluble vitamin that is essential for human health, and its excessive intake will accumulate in fat tissue and produce toxicity, and the average adult is not deficient in vitamin D due to frequent exposure to sunlight. At the same time, vitamin D deficiency is common worldwide, and its deficiency can lead to reduced absorption of calcium and phosphate, affecting bone health. In addition, the main way the body supplements vitamin D is through sun exposure and diet.
| Research Area | Metabolism |
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