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Product Description
Plasmid DNA Extraction Mini Kit (100prep) (sample size:1~3 ml culture) is available at Gentaur for next week delivery.Store RNase A at -20 °C upon recipit of kit.
Store RNase A at -20 °C upon recipit of kit.
Add 0.5 ml of PD1 Buffer to a RNase A tube, Dissolve the RNase A by vortexing. Briefly spin the tube and transfer the total RNase A mixture back to the PD1 bottle, mix well by vortexing and store the PD1 buffer at 4 °C.
If precipitates have formed in PD2 Buffer, warm the buffer in 37°C waterbath to dissolve precipitates.
Preparation of PDW Buffer and Wash Buffer by adding 96 ~100% ethanol (not provided) for first use.
Centrifugation steps are done by a microcentrifuge capable of the speed at 11,000 ~1,8000 x g.Add 0.5 ml of PD1 Buffer to a RNase A tube, Dissolve the RNase A by vortexing. Briefly spin the tube and transfer the total RNase A mixture back to the PD1 bottle, mix well by vortexing and store the PD1 buffer at 4 °C.
If precipitates have formed in PD2 Buffer, warm the buffer in 37°C waterbath to dissolve precipitates.
Preparation of PDW Buffer and Wash Buffer by adding 96 ~100% ethanol (not provided) for first use.
Centrifugation steps are done by a microcentrifuge capable of the speed at 11,000 ~1,8000 x g.
