Rat PTGS2/COX-2(Prostaglandin Endoperoxide Synthase 2) ELISA Kit (E-EL-R0792)
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For research use only.
Product Summary
| Sensitivity | 75 pg/mL |
| Detection Range | 125-8000 pg/mL |
| Sample Volume | 100 μL |
| Total Assay Time | 3 h 30 min |
| Reactivity | Rat |
| Specificity | This kit recognizes Rat PTGS2/COX-2 in samples. No significant cross-reactivity or interference between Rat PTGS2/COX-2 and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, EDTA plasma, Urine, Tissue homogenate and Cell lysate |
| 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 Rat PTGS2 were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Rat PTGS2 were tested on three separate plates, with 20 replicates per plate, to assess variability among assays.
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| Recovery |
The recovery of Rat PTGS2 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 Rat PTGS2 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 Rat PTGS2/COX-2. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Rat PTGS2/COX-2 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 Rat PTGS2/COX-2, 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 Rat PTGS2/COX-2. You can calculate the concentration of Rat PTGS2/COX-2 in the samples by comparing the OD of the samples to the standard curve.
Background
Prostaglandin-endoperoxide synthase 2 (PTGS2), also known as cyclooxygenase 2 (COX-2), is a bifunctional membrane-bound enzyme that catalyzes a key rate-limiting step in prostaglandin synthesis. It displays both cyclooxygenase and peroxidase activities, converting arachidonic acid into prostaglandin H2 (PGH2), the common precursor of active prostanoids including prostaglandin E2 (PGE2) and prostacyclin. COX-2 is an inducible isoform that is weakly expressed in most normal tissues and rapidly upregulated by inflammatory cytokines, endotoxin, growth factors and tissue injury.
Unlike the constitutively expressed COX-1, COX-2 mediates the burst synthesis of prostaglandins during inflammation, pain and fever, generating large amounts of PGE2 that sensitize nociceptors, promote vasodilation and edema and raise the hypothalamic temperature set point. COX-2-derived prostanoids also contribute to physiological processes such as ovulation, implantation, renal blood flow regulation and vascular homeostasis.
COX-2 is a major target of non-steroidal anti-inflammatory drugs (NSAIDs), and selective COX-2 inhibitors were developed to reduce gastrointestinal toxicity; its overexpression is also associated with colorectal and other tumors. This ELISA kit enables quantitative determination of rat COX-2 in cell and tissue lysates, and is applied in studies of inflammation, nociception and carcinogenesis.
| Gene ID | 29527 |
| Uniport ID | P35355 |
| Research Area | Cancer , Cardiovascular , Metabolism , SignalTransduction |
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