Mouse MMP-13(Matrix Metalloproteinase 13) ELISA Kit (E-EL-M0076)
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For research use only.
Product Summary
| Sensitivity | 46.88 pg/mL |
| Detection Range | 78.13-5000 pg/mL |
| Sample Volume | 100 μL |
| Total Assay Time | 3 h 30 min |
| Reactivity | Mouse |
| Specificity | This kit recognizes Mouse MMP-13 in samples. No significant cross-reactivity or interference between Mouse MMP-13 and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, EDTA plasma, Urine, Tissue homogenate and Cell culture supernatant |
| Detection Method | Colorimetric method, ELISA, Sandwich |
| Assay Type | Sandwich-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 Mouse MMP-13 were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Mouse MMP-13 were tested on three separate plates, with 20 replicates per plate, to assess variability among assays.
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| Recovery |
The recovery of Mouse MMP-13 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 Mouse MMP-13 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 Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Mouse MMP-13. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Mouse MMP-13 and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Mouse MMP-13, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Mouse MMP-13. You can calculate the concentration of Mouse MMP-13 in the samples by comparing the OD of the samples to the standard curve.
Background
Mouse adrenocorticotropic hormone (ACTH), also called corticotropin, is a 39-amino-acid polypeptide derived by proteolytic processing of pro-opiomelanocortin (POMC). It is produced mainly by corticotroph cells of the anterior pituitary, with smaller amounts generated in the hypothalamus, skin, and immune cells. Secretion is stimulated by hypothalamic corticotropin-releasing hormone and vasopressin, follows a pronounced circadian rhythm, and is suppressed by glucocorticoid negative feedback.
ACTH acts principally through the melanocortin 2 receptor (MC2R) on adrenal cortical cells to stimulate glucocorticoid synthesis and secretion and to maintain adrenal cortical growth and steroidogenic capacity. Receptor binding activates the cyclic AMP-protein kinase A pathway and upregulates steroidogenic enzymes and cholesterol mobilization, positioning ACTH as the central effector of the hypothalamic-pituitary-adrenal axis during stress. Additional melanocortin receptors mediate effects on pigmentation and lipid metabolism.
Circulating ACTH is used to evaluate integrity of the hypothalamic-pituitary-adrenal axis, to distinguish primary from secondary adrenal insufficiency, and to investigate Cushing disease; paired measurement with cortisol helps localize the lesion. This ELISA kit enables quantitative determination of mouse ACTH in serum, plasma, and cell culture supernatant, supporting dynamic endocrine testing, stress neuroendocrine research, and studies of pituitary-adrenal regulation.
| Uniport ID | P33435 |
| Research Area | Cancer , Cardiovascular , CellBiology , SignalTransduction |
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