96-well plate DNA/RNA extraction kit

Here are some ways to ensure the effectiveness of the 96-well plate DNA/RNA extraction kit:
Strictly follow the instructions: Make sure that the conditions and timing of each step are accurate.
Use high-quality samples: The quality of the samples has a great influence on the extraction effect, try to use fresh, high-quality biological samples.
Control the experimental environment: Keep the experimental environment clean to avoid cross-contamination.
Adjust the experimental parameters appropriately: according to the characteristics of the samples, it may be necessary to adjust the lysis time, temperature and other parameters appropriately.
Perform adequate washing: remove impurities thoroughly to improve the purity of nucleic acids.
Avoid nuclease contamination: Use nuclease-free consumables and reagents, and pay attention to prevent nuclease contamination during operation.
Perform quality testing: Perform quality testing of nucleic acids after extraction, such as concentration, purity, etc., to ensure that it meets the requirements of subsequent experiments.

The following are general directions for use of the 96-well plate DNA/RNA Extraction Kit:
Preparation: Remove the reagents and consumables from the kit and equilibrate to room temperature.
Sample treatment: Add the biological samples to be extracted (e.g., cells, tissues, etc.) into the corresponding wells, and carry out lysis and other treatments according to the requirements of the kit.
Nucleic acid adsorption: according to the instructions of the kit, mix the processed sample with the extraction reagent to bind nucleic acids to the adsorption medium.
Wash step: several washes are performed to remove impurities.
Nucleic acid elution: Add elution solution to elute the adsorbed nucleic acids.
Collection of nucleic acids: the eluted nucleic acid solution is collected and can be used for subsequent experiments or preservation.