SP(Substance P) ELISA Kit (E-EL-0067)
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For research use only.
Product Summary
| Sensitivity | 46.88 pg/mL |
| Detection Range | 78.13-5000 pg/mL |
| Sample Volume | 50 μL |
| Total Assay Time | 2 h 30 min |
| Reactivity | Universal |
| Specificity | This kit recognizes Universal SP in samples.No significant cross-reactivity or interference between Universal SP 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 SP were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Universal SP 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 SP 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 SP 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 SP. During the reaction, Universal SP in the sample or standard competes with a fixed amount of Universal SP on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Universal SP. 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 SP in tested samples can be calculated by comparing the OD of the samples to the standard curve.
Background
Substance P (SP) is an eleven-amino-acid peptide of the tachykinin family generated by proteolytic processing of the product of the TAC1 gene and closely related to neurokinin A. It is distributed in the central and peripheral nervous systems, particularly in unmyelinated sensory C-fiber terminals, in the spinal dorsal horn, in enteric neurons and in the intestinal mucosa, where it acts as a neurotransmitter and a local mediator of neurogenic responses.
As the preferred ligand of the neurokinin-1 receptor (NK1R), substance P activates phospholipase C and mobilizes intracellular calcium, thereby transmitting and amplifying nociceptive signals in the spinal dorsal horn. As a mediator of neurogenic inflammation it promotes vasodilation and plasma extravasation, activates mast cells, recruits immune cells and sensitizes nociceptors.
Measurement of substance P supports research on pain, itch and inflammation. The pathway is a therapeutic target in chemotherapy-induced nausea and vomiting, where NK1R antagonists are used, and levels rise in arthritis, asthma, inflammatory bowel disease and migraine. Quantitation in serum, plasma, tissue and cerebrospinal fluid helps evaluate NK1R-directed interventions and neuroimmune activity.
| Uniport ID | H:P20366 M:P41539 R:P06767 |
| Research Area | Cardiovascular , Neuroscience |
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