EPI(Epinephrine/Adrenaline) ELISA Kit (E-EL-0045)
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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 | Universal |
| Specificity | This kit recognizes Universal EPI in samples.No significant cross-reactivity or interference between Universal EPI and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Human: Serum, EDTA plasma, heparinized plasma, Saliva, Urine, Semen and Stool; Mouse: Serum, EDTA plasma, Urine and Tissue homogenate; Rat: Serum, EDTA plasma, Urine and Tissue homogenate; Cell lysate, 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 Universal EPI were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Universal EPI were tested on three separate plates, with 20 replicates per plate, to assess variability among assays.
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| Recovery |
The recovery of Universal EPI 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 Universal EPI 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 Universal EPI. During the reaction, Universal EPI in the sample or standard competes with a fixed amount of Universal EPI on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Universal EPI. 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 Universal EPI in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Background
Epinephrine, also called adrenaline, is a catecholamine of formula C9H13NO3 secreted by the chromaffin cells of the adrenal medulla and also acting as a neurotransmitter at some central and peripheral synapses. Within the medulla it is synthesized from norepinephrine by phenylethanolamine N-methyltransferase, stored in chromaffin granules and released into the blood upon sympathetic stimulation.
It is the principal hormonal mediator of the fight-or-flight response and is secreted in large amounts during fear, exercise, hypoglycemia or danger. Acting through alpha- and beta-adrenergic receptors it increases heart rate and cardiac output, raises blood pressure, dilates bronchi and mobilizes energy substrates by stimulating glycogenolysis and lipolysis while redistributing regional blood flow toward skeletal muscle, dilating the pupils and reducing gastrointestinal motility.
Measurement of epinephrine in plasma or urine is important for assessing sympathoadrenal activity, and markedly elevated values are associated with pheochromocytoma and other catecholamine-secreting tumors that cause hypertension. Because the catecholamine is rapidly metabolized and fluctuates with posture and stress, standardized collection and prompt stabilization of samples are essential for reliable determination.
| Research Area | Cancer , Cardiovascular , CellBiology , Metabolism , Neuroscience , SignalTransduction |
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