Learn more about RNA extraction technology for getting purified RNA easily!


RNA is an intermediate product of gene expression and exists in the cytoplasm and nucleus. RNA extraction is the basis of molecular biology research. High-quality, high-purity and high-integrity of is required for downstream molecular biology experiments such as cDNA library construction, in vitro reverse transcription, real-time fluorescence quantitative PCR, and Northern hybridization analysis. However, RNA is very “delicate”, and it will fail to be extracted if not carefully enough.

1. Introduction to RNA

RNA is the abbreviation of RiboNucleicAcid, which is a genetic information carrier existing in biological cells and some viruses and viroids. RNA is a long chain molecule formed by the condensation of ribonucleotides through phosphodiester bonds. Unlike DNA, RNA is generally a single-stranded long molecule. Using one DNA strand as a template and the principle of base complementary pairing, a single strand is formed by transcription. Its main function is to realize the expression of genetic information on proteins, and it is a bridge in the process of transforming genetic information to phenotype. Some organisms, such as SARS-CoV-2, also directly use RNA as a carrier of genetic information.

2. Principles of RNA extraction

The essence of total RNA extraction from different tissues is to lyse cells, release RNA, and remove impurities such as polysaccharides, phenols, proteins, and DNA in different ways, and finally obtain high-purity RNA products through a series of extraction, washing and precipitation. There are four main principles for RNA extraction: 1. Ensure the integrity of the primary structure of RNA; 2. There should be no organic solvents that inhibit the enzyme and high concentrations of metal ions in the extracted RNA samples; 3. The contamination of other biological macromolecules such as proteins, polysaccharides and lipid molecules should be minimized; 4. The contamination of other nucleic acid molecules (DNA) should be excluded.

3. The evolution of RNA extraction technology

With the in-depth research and wide application of RNA, RNA extraction technology has also been greatly developed, from the widely used traditional manual RNA extraction to automated RNA extraction by nucleic acid extractors.


( 1 ) Traditional manual RNA extraction technology

Early RNA extraction techniques

The early RNA extraction technology was guanidine isothiocyanate cesium chloride ultracentrifugation, the principle of which was to use the protein denaturing agent guanidine isothiocyanate to effectively inhibit the activity of RNase. Density gradient ultracentrifugation in cesium chloride medium precipitates RNA at the bottom of the tube. However, this extraction method is complicated in operation, long in process, limited in the number of samples extracted at one time, and requires high experimental equipment. Later, in order to solve the problem of lack of scientific research equipment such as ultracentrifugation, scientists proposed the guanidine hydrochloride-organic solvent method, which uses guanidine salts to inhibit RNase, homogenize cells to lyse, extract proteins with organic solvents, and remove DNA by selectively precipitating RNA molecules. , Although this method solves the problem of no ultracentrifuge, the whole operation process is still complicated and time-consuming.

RNA extraction technology by Trizol method

With the development of science and technology, there have been many techniques for manually extracting and purifying RNA, the most classic of which is the Trizol method. The main components of Trizol reagent are phenol and guanidine isothiocyanate. The main function of phenol is to lyse cells, so that the protein and nucleic acid substances in the cells are depolymerized and released. Although phenol can effectively denature proteins, it cannot completely inhibit RNase activity. Guanidine isothiocyanate is a powerful protein denaturing agent, which can not only dissolve proteins rapidly, resulting in the fragmentation of cell structures, and the rapid separation of nucleoproteins from nucleic acids due to the destruction and disappearance of their secondary structures, but also has a strong denaturing effect on RNases. When chloroform is added, it can extract the acidic phenol, which can promote the RNA into the aqueous phase, and after centrifugation can form the aqueous and organic layers, so that the RNA is separated from the protein and DNA remaining in the organic phase. The aqueous layer (colorless) is mainly RNA, and the organic layer (yellow) is mainly DNA and protein. Trizol reagent can be used not only for small samples, but also for a large number of samples. It is suitable for animal, plant, bacteria, blood extraction, and can process a large number of different samples at the same time.