Rat ANP(Atrial Natriuretic Peptide) ELISA Kit (E-EL-R0017)
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For research use only.
Product Summary
| Sensitivity | 9.38 pg/mL |
| Detection Range | 15.63-1000 pg/mL |
| Sample Volume | 50 μL |
| Total Assay Time | 2 h 30 min |
| Reactivity | Rat |
| Specificity | This kit recognizes Rat ANP in samples.No significant cross-reactivity or interference between Rat ANP 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 ANP were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Rat ANP 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 ANP 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 ANP 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 ANP. During the reaction, Rat ANP in the sample or standard competes with a fixed amount of Rat ANP on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Rat ANP. 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 ANP in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Background
Microalbuminuria (MAU) denotes a slight but abnormal increase in urinary albumin excretion that remains below the detection threshold of conventional dipstick tests. Albumin is synthesized by hepatocytes, maintains plasma colloid osmotic pressure and serves as a transport vehicle for fatty acids, bilirubin, hormones and many drugs. Because of its relatively small size and net negative charge, only trace quantities cross the glomerular filtration barrier under physiological conditions, and nearly all filtered albumin is reclaimed by receptor-mediated endocytosis in the proximal tubule.
Functionally albumin is a multifunctional carrier and the principal determinant of plasma oncotic pressure, and tubular reclamation prevents urinary protein loss. When diabetes, hypertension or primary glomerular disease damages the filtration barrier, altering its size- and charge-selective properties, filtered albumin exceeds tubular reabsorptive capacity and urinary excretion rises. Microalbuminuria therefore occupies the intermediate zone between normal excretion and overt proteinuria and reflects early, potentially reversible glomerular injury.
Microalbuminuria is an early and sensitive marker of glomerular damage that predicts progression of diabetic nephropathy and cardiovascular risk and additionally signals widespread endothelial dysfunction. This ELISA kit enables quantitative determination of rat albumin in urine, serum and plasma for the assessment of microalbuminuria, supporting studies of diabetic, hypertensive and nephrotoxic kidney injury and renoprotective interventions.
| Gene ID | 24602 |
| Uniport ID | P01161 |
| Research Area | Cancer , Cardiovascular , SignalTransduction |
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