Human CRP(C-Reactive Protein) ELISA Kit (E-EL-H0043)
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For research use only.
Product Summary
| Sensitivity | 0.23 ng/mL |
| Detection Range | 0.39-25 ng/mL |
| Sample Volume | 100 μL |
| Total Assay Time | 3 h 30 min |
| Reactivity | Human |
| Specificity | This kit recognizes Human CRP in samples. No significant cross-reactivity or interference between Human CRP and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, EDTA plasma, heparinized plasma, Saliva, breast milk, Urine, 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 CRP were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Human CRP 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 CRP 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 CRP 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 CRP. 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 CRP 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 CRP, 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 CRP. You can calculate the concentration of Human CRP in the samples by comparing the OD of the samples to the standard curve.
Background
C-reactive protein (CRP), also designated pentraxin 1, is a non-glycosylated member of the pentraxin family. It is synthesized mainly by hepatocytes and assembled as a cyclic pentamer of about 110-120 kDa. In humans CRP is a major acute-phase protein whose circulating concentration rises sharply during inflammation, where it acts as a sensor and activator of innate immunity. Transcription is driven mainly by interleukin-6 (IL-6), whereas in mice pentraxin 2 compensates, illustrating species differences.
Through the ligand-binding face of its pentamer, CRP recognizes damaged self structures and microbial targets. It binds and opsonizes apoptotic cells and bacteria such as Streptococcus pneumoniae to enhance phagocytosis, and engages complement components including C1q, C4b-binding protein and factor H, promoting classical-pathway activation while limiting terminal lysis. Engagement of Fc gamma receptors links this humoral recognition to cellular effector functions.
Because of its IL-6-driven dynamic response, CRP is the most widely used marker of inflammation and infection. Concentrations increase in bacterial infection, postoperative complications, active autoimmune disease and elevated cardiovascular risk, and serial measurement allows therapeutic response to be assessed. CRP therefore remains a first-line laboratory indicator of systemic inflammatory activity.
| Gene ID | 1401 |
| Uniport ID | P02741 |
| Research Area | Cancer , Cardiovascular , EpigeneticsandNuclearSignaling , Immunology , Metabolism |
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