Product Number: RNK5301
Shipping and Storage
Components
Component | Storage | RNK5301 50Preps |
Buffer CLB | RT | 50 ml |
Buffer RLT Plus | RT | 25 ml |
Buffer RW1 | RT | 40 ml |
Buffer RW | RT | 10 ml |
RNase-free H2O | RT | 10 ml |
Genomic DNA clearance column and collection tube | RT | 50 |
RNase free adsorption column RA and collection tube | RT | 50 |
Description
On the basis of our company's exclusive introduction of EASYspin phenol free and chloroform based rapid RNA extraction technology, we have also independently developed the genome DNA clearance column technology, which can effectively remove gDNA residues. The obtained RNA generally does not require DNase digestion and can be used for reverse transcription PCR, fluorescence quantitative PCR and other experiments. The unique Buffer CLB and Buffer RLT Plus rapidly lyse cells and inactivate cell RNA enzymes. Centrifuge precipitation is used to remove polysaccharides, polyphenols, and secondary metabolites. Then, the mixture is lysed and ethanol is used to regulate RNA binding and adsorption onto the genomic DNA clearance column. RNA is selectively washed and filtered, and the residual DNA adsorbed on the genomic DNA clearance column cannot be washed off. The column is discarded together to remove DNA. After adjusting the binding conditions with ethanol, the filtered RNA selectively adsorbs onto the silica matrix membrane in a highly dissociated salt state. Through a series of rapid rinsing centrifugation steps, Buffer RW1 and Buffer RW remove impurities such as cell metabolites and proteins. Finally, low salt RNase free H2O washes the pure RNA off the silica matrix membrane.
Features
Application
Suitable for rapid extraction of total RNA from plant tissue cells, unique genomic DNA clearance column technology can effectively remove visible gDNA residues on electrophoresis. RNA can be used for reverse transcription PCR, fluorescence quantitative PCR, etc.