General Notes | 1. After removing the kit from the refrigerator, allow it to equilibrate at room temperature for 1 hour before use. If the enzyme-coated plate is opened and not completely used, store it in a sealed bag. 2. Crystals may form in the concentrated wash buffer. Warming in a water bath can aid dissolution during dilution. This will not affect the results. 3. Use a pipette for each sample addition step and frequently calibrate its accuracy to avoid experimental error. The time for each addition should ideally be within 5 minutes. For large numbers of samples, using a dispenser is recommended. 4. Develop a standard curve with each measurement, preferably with replicates. If the analyte content in the sample is too high (the sample OD value is greater than the OD value of the first standard well), dilute the sample a certain number of times (n times) with sample diluent before measurement. When calculating the final dilution, multiply by the total dilution factor (×n×5). 5. The sealing film is for single use only to avoid cross contamination. 6. Please store the substrate in a dark place. 7. Strictly follow the instructions for operation. The test results must be determined based on the readings of the microplate reader. 8. All samples, washing solutions and various wastes should be treated as infectious materials. 9. Components of different batches of this reagent must not be mixed. |