Rabbit IgG(Immunoglobulin G) ELISA Kit (E-EL-RB2288)
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For research use only.
Product Summary
| Sensitivity | 0.38 μg/mL |
| Detection Range | 0.63-40 μg/mL |
| Sample Volume | 50 μL |
| Total Assay Time | 2 h 30 min |
| Reactivity | Rabbit |
| Specificity | This kit recognizes Rabbit IgG in samples.No significant cross-reactivity or interference between Rabbit IgG 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 Rabbit IgG 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 Rabbit IgG 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 Rabbit IgG. During the reaction, Rabbit IgG in the sample or standard competes with a fixed amount of Rabbit IgG on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Rabbit IgG. 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 Rabbit IgG in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Background
Immunoglobulin G is the main component of serum immunoglobulin, accounting for about 75% of the total content of serum immunoglobulin, and the normal value is 9.5~12.5mg无ml. Of these, 40-50% are distributed in the serum, and the rest are distributed in the tissue. The molecular weight is about 150,000 Daltons.
Because IgG can cross the placenta, the IgG acquired by the newborn from the mother plays an important role in fighting infection. IgG synthesis begins 2 to 4 weeks after birth, and serum IgG can reach adult levels after 8 years of age. Because IgG is more easily diffused into the space outside blood vessels than other Ig, it plays an important role in binding complement, enhancing the ability of immune cells to phagocytic pathogenic microorganisms and neutralizing bacterial toxins, and can effectively fight infection, which is a favorable side for human body. However, in some autoimmune diseases, such as autoimmune hemolytic anemia, thrombocytopenic purpura, lupus erythematosus and rheumatoid disease, the autoantibodies are IgG. Once it binds to the corresponding own cells, it instead enhances the tissue damage effect.
| Research Area | CellBiology |
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