Human IgG(Immunoglobulin G) ELISA Kit (E-EL-H0169)
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For research use only.
Product Summary
| Sensitivity | 0.94 ng/mL |
| Detection Range | 1.56-100 ng/mL |
| Sample Volume | 100 μL |
| Total Assay Time | 3 h 30 min |
| Reactivity | Human |
| Specificity | This kit recognizes Human IgG in samples. No significant cross-reactivity or interference between Human IgG and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, EDTA plasma, heparinized plasma, Saliva, breast milk, Urine, Semen, Stool and Cell culture supernatant |
| Detection Method | Colorimetric method, ELISA, Sandwich |
| Assay Type | Sandwich-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 IgG were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Human IgG were tested on three separate plates, with 20 replicates per plate, to assess variability among assays.
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| Recovery |
The recovery of Human 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 Human 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 Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human IgG. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Human IgG and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Human IgG, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human IgG. You can calculate the concentration of Human IgG in the samples by comparing the OD of the samples to the standard curve.
Background
Immunoglobulin G (IgG) is the most abundant immunoglobulin in human serum and the principal mediator of humoral immunity. Each molecule consists of two heavy chains and two light chains, with the heavy-chain constant region defining the class and each antigen-binding site formed by the variable domains of one heavy and one light chain, giving two binding sites per molecule. Four subclasses exist, differing in effector functions such as complement activation and Fc receptor binding.
During immune recognition, membrane-bound immunoglobulin serves as the B-cell antigen receptor, and antigen binding triggers clonal expansion and differentiation into plasma cells. Secreted IgG clears antigen by neutralization, opsonization and complement activation. Diversity and affinity maturation arise from V-(D)-J rearrangement and somatic hypermutation of the variable regions, generating high-affinity, long-lived protective antibodies that underpin immunological memory and vaccination.
Because IgG constitutes the bulk of serum antibodies and confers long-term protection, its measurement is fundamental to assessing humoral immunity. This ELISA kit enables quantitative determination of total IgG in serum, supporting investigation of primary and secondary immunodeficiency, chronic infection and monoclonal gammopathy, while subclass analysis aids evaluation of vaccine responses in clinical immunology and immune-competence monitoring.
| Gene ID | 7083 |
| Uniport ID | P01860 |
| Research Area | Immunology |
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