Human GHRL(Ghrelin) ELISA Kit (E-EL-H1919)
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For research use only.
Product Summary
| Sensitivity | 0.1 ng/mL |
| Detection Range | 0.16-10 ng/mL |
| Sample Volume | 50 μL |
| Total Assay Time | 2 h 30 min |
| Reactivity | Human |
| Specificity | This kit recognizes Human GHRL in samples.No significant cross-reactivity or interference between Human GHRL 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 GHRL were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Human GHRL 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 GHRL 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 GHRL 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 GHRL. During the reaction, Human GHRL in the sample or standard competes with a fixed amount of Human GHRL on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Human GHRL. 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 GHRL in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Background
Somatostatin, also known as growth hormone-inhibiting hormone (GHIH), is a peptide hormone that inhibits the release of numerous hormones through G protein-coupled receptors. It is processed from a larger precursor into two bioactive forms, a 14-amino-acid and a 28-amino-acid peptide, is widely distributed in the central and peripheral nervous system, the gastrointestinal tract and the endocrine pancreas where delta cells are the main source, and is stored in secretory granules for stimulus-dependent release.
Somatostatin acts through a family of five receptors, SSTR1 to SSTR5, that couple to Gi to inhibit adenylyl cyclase, reduce calcium influx and modulate potassium channels. In the anterior pituitary it suppresses growth hormone, thyroid-stimulating hormone and prolactin secretion, and in the gastrointestinal system it inhibits gut and pancreatic hormones including gastrin and cholecystokinin, slows gastric emptying, reduces intestinal motility, secretion and splanchnic blood flow, and inhibits insulin and glucagon release as an intraislet paracrine regulator.
Because of these broad inhibitory actions, somatostatin serves as a brake on endocrine and exocrine secretion and on cell proliferation, and long-acting synthetic analogs such as octreotide and lanreotide are used to treat acromegaly and hormone-secreting neuroendocrine tumors. Measurement of somatostatin supports studies of neuroendocrine regulation, gastrointestinal physiology, control of growth hormone, insulin and glucagon secretion, and evaluation of neuroendocrine tumors.
| Gene ID | 51738 |
| Uniport ID | Q9UBU3 |
| Research Area | Cancer , Cardiovascular , Metabolism , Neuroscience , SignalTransduction |
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