Details

The Total RNA Mini Kit (Plant) provides an efficient method for purifying total RNA from plant tissue and cells. Samples are ground in liquid nitrogen and then filtered to remove cell debris. In the presence of a binding buffer and chaotropic salt, total RNA in the lysate binds to the glass fiber matrix of the spin column (1). Optional DNase treatments can be followed to remove unwanted DNA residue. Once any contaminants have been removed using the Wash Buffer (containing ethanol), the purified total RNA is eluted by RNase-Free Water. The procedure does not require phenol extraction or alcohol precipitation and can be completed within 1 hour. The purified total RNA is ready for use in RT, RT-PCR, Real-time PCR and Northern Blotting.

Quality Control

The quality of the Total RNA Mini Kit (Plant) is tested on a lot-to-lot basis by isolating total RNA from a 25 mg young leaf sample. The Purified RNA is quantified with a spectrophotometer and checked by electrophoresis.