Rat BNP(Brain Natriuretic Peptide) ELISA Kit (E-EL-R0126)
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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 | Rat |
| Specificity | This kit recognizes Rat BNP in samples.No significant cross-reactivity or interference between Rat BNP and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, EDTA plasma, Urine, Tissue homogenate 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 Rat BNP were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Rat BNP 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 BNP 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 BNP 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 Rat BNP. During the reaction, Rat BNP in the sample or standard competes with a fixed amount of Rat BNP on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Rat BNP. 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 Rat BNP in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Background
B-type natriuretic peptide (BNP), also known as brain natriuretic peptide, is a nonglycosylated peptide hormone of the natriuretic peptide family, characterized by a conserved intramolecular disulfide ring, and is produced predominantly by ventricular cardiomyocytes although it was first identified in porcine brain. Transcription and release rise markedly when myocardial wall stress increases with pressure overload or volume expansion, and the precursor preproBNP is cleaved to yield the inactive amino-terminal fragment NT-proBNP together with biologically active BNP.
BNP serves to unload the volume-overloaded or failing heart. Binding to the guanylyl cyclase-coupled receptor NPR1 raises intracellular cGMP, producing vasodilation and natriuresis that lower cardiac preload and afterload, while antagonizing the renin-angiotensin-aldosterone system, sympathetic outflow and maladaptive hypertrophy and fibrosis. The N-terminal fragment NT-proBNP lacks biological activity but is cleared more slowly and is therefore a more stable circulating analyte.
Plasma BNP and NT-proBNP are established biomarkers in cardiovascular medicine, used for heart failure diagnosis, risk stratification and treatment monitoring. This ELISA kit enables quantitative determination of rat BNP in serum and plasma, supporting evaluation of cardiac loading, ventricular remodeling and responses to pathological stress or cardiovascular therapy.
| Gene ID | 25105 |
| Uniport ID | P13205 |
| Research Area | Cancer , Cardiovascular , Neuroscience |
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