Rat CKMB(Creatine Kinase MB Isoenzyme) ELISA Kit (E-EL-R1327)
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For research use only.
Product Summary
| Sensitivity | 18.75 pg/mL |
| Detection Range | 31.25-2000 pg/mL |
| Sample Volume | 100 μL |
| Total Assay Time | 3 h 30 min |
| Reactivity | Rat |
| Specificity | This kit recognizes Rat CKMB in samples. No significant cross-reactivity or interference between Rat CKMB and analogues was observed |
| Recovery | 80%-120% |
| Sample Type | Serum, EDTA plasma, Urine, Tissue homogenate and Cell lysate |
| 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 Rat CKMB were tested 20 times on a single plate.
Inter-assay Precision (Between-run Precision): Three samples representing low, mid, and high concentrations of Rat CKMB were tested on three separate plates, with 20 replicates per plate, to assess variability among assays.
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| Recovery |
The recovery of Rat CKMB 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 Rat CKMB 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 Rat CKMB. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Rat CKMB 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 Rat CKMB, 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 Rat CKMB. You can calculate the concentration of Rat CKMB in the samples by comparing the OD of the samples to the standard curve.
Background
Creatine kinase MB isoenzyme (CK-MB) is a cytosolic enzyme formed as a heterodimer of muscle (M) and brain (B) subunits. It catalyzes the reversible transfer of phosphate between ATP and creatine to generate phosphocreatine, thereby providing a rapidly mobilizable high-energy phosphate reserve for tissues with high and fluctuating energy demand such as the myocardium, where it accounts for roughly 15-30% of total creatine kinase activity.
Physiologically, CK-MB regenerates ATP from phosphocreatine when energy demand rises, sustaining myocardial contraction and ion pump function. When cardiomyocytes are injured and membrane integrity is lost, cytosolic CK-MB escapes into the circulation in proportion to the extent of necrosis; after acute myocardial infarction its level rises within a few hours, peaks at about one day and returns to baseline within two to three days.
CK-MB was long a cornerstone of myocardial infarction diagnosis and remains useful for detecting reinfarction, and it is also elevated in myocarditis, after cardiac surgery and in severe skeletal muscle injury. This ELISA kit enables quantitative determination of rat CK-MB in serum and plasma, and it is used in myocardial injury and ischemia-reperfusion studies as a classic indicator of myocardial necrosis.
| Gene ID | 24264, 24265 |
| Uniport ID | P00564 P07335 |
| Research Area | Cardiovascular , Metabolism , SignalTransduction |
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