Description
RNA Extraction is designed to isolate total RNA from a variety of sample types for molecular biology applications such as isothermal amplification, real-time PCR, and reverse transcription PCR (RT-PCR).
The principle of this method relies on the lysis buffer activity to denature and lyse cells for RNA extraction, and the RNA binds to the silica gel membrane in the spin column. The unique buffer chemistry enables selective nucleic acid binding of RNA. All buffer components are quality control checked for RNase contamination.
Features