ACH(Acetylcholine) ELISA Kit (E-EL-0081)
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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 | Universal |
| Specificity | This kit recognizes Universal ACH in samples.No significant cross-reactivity or interference between Universal ACH and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, plasma and other biological fluids |
| 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 IL-6 were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Human IL-6 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 ACH 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 ACH 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 ACH. During the reaction, Universal ACH in the sample or standard competes with a fixed amount of Universal ACH on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Universal ACH. 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 ACH in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Background
Acetylcholine is a neurochemical that has a wide variety of functions in the brain and other organ systems of the body. Specifically, it is a neurotransmitter that acts as a chemical message that is released by neurons and allows them to communicate with one another and other specialized cells such as myocytes and cells found in glandular tissues. The name "acetylcholine" is derived from its chemical structure, as it is an ester of acetic acid and choline. Tissues of the body that use this chemical messenger or are responsive to it are referred to as cholinergic. There is a class of chemicals called anticholinergics that interfere with acetylcholine's action on tissues as well. While ACh operates as a neurotransmitter in many parts of the body, it is most commonly associated with the neuromuscular junction. The neuromuscular junction is where motor neurons located in the ventral spinal cord synapse with muscles in the body to activate them. Acetylcholine also functions as a neurotransmitter in the autonomic nervous system, acting both as the neurotransmitter between preganglionic and postganglionic neurons as well as being the final release product from parasympathetic postganglionic neurons.
| Research Area | Neuroscience , Signal Transduction , Immunology |
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