Human Ang-Ⅱ(Angiotensin Ⅱ) ELISA Kit (E-EL-H0326)
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For research use only.
Product Summary
| Sensitivity | 18.75 pg/mL |
| Detection Range | 31.25-2000 pg/mL |
| Sample Volume | 50 μL |
| Total Assay Time | 2 h 30 min |
| Reactivity | Human |
| Specificity | This kit recognizes Human Ang-Ⅱ in samples.No significant cross-reactivity or interference between Human Ang-Ⅱ and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, EDTA plasma, heparinized plasma, breast milk, Urine and Cell culture supernatant |
| 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 Ang-Ⅱ were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Human Ang-Ⅱ 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 Ang-Ⅱ 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 Ang-Ⅱ 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 Human Ang-Ⅱ. During the reaction, Human Ang-Ⅱ in the sample or standard competes with a fixed amount of Human Ang-Ⅱ on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Human Ang-Ⅱ. 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 Human Ang-Ⅱ in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Background
Angiotensin II (Ang-II) is the principal effector peptide of the renin-angiotensin system. This octapeptide is generated from liver-derived angiotensinogen by the sequential action of renin, which releases the decapeptide angiotensin I, and angiotensin-converting enzyme, which acts mainly in the lung and vascular endothelium. Ang-II is degraded rapidly and functions both as a circulating hormone and as a locally produced tissue peptide, becoming activated when renal perfusion falls.
Ang-II acts chiefly through the AT1 receptor, with a lesser contribution from AT2, and is a potent vasoconstrictor that also increases myocardial contractility, renal sodium retention, aldosterone secretion, sympathetic outflow, inflammation, fibrosis and oxidative stress. In the adrenal cortex it stimulates aldosterone release, and in the kidney it constricts efferent arterioles and enhances sodium reabsorption. The AT2 receptor and the Ang-(1-7)/Mas axis partly antagonize these effects, and their balance determines the net outcome.
Excessive Ang-II activity contributes to hypertension, heart failure, chronic kidney disease and atherosclerosis, and its quantification assesses renin-angiotensin system activity. As the target of angiotensin-converting enzyme inhibitors and angiotensin receptor blockers, accurate measurement supports hypertension research and monitoring of renin-system-directed therapy that has transformed cardiorenal management, and assists individualized treatment.
| Gene ID | 183 |
| Uniport ID | P01019 |
| Research Area | Cancer , Cardiovascular , Metabolism , SignalTransduction |
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