Cryolys Evolution

Obtaining high-quality, high-yield DNA from a sample requires an optimal homogenization process. Below, our team of scientists share helpful tips to choose the right homogenization protocol for your DNA extraction

RNA isolation can often be challenging, particularly when working with complex samples. Common difficulties included low yield, low purity, RNA degradation, and DNA contamination. Below, Bertin’s team of scientists have shared best practices for homogenization protocols that allow for successful isolation of high-quality RNA.

Protein extraction is a key step for analytical methods such as Western Blot and enzymatic assays. Below, Bertin’s top scientists have shared best practices to improve your homogenization protocol for a wide range of tissues, including tips to preserve the integrity of the proteins in your samples and achieve optimal yield.

The disruption of samples is the first step in the process of isolation and/or quantification of nucleic acids, proteins, and analytes. For this reason, choosing the right homogenization protocol will have a great impact on the quality and reliability of results for most biological analytical workflows.

PCR is a vital analytical tool for modern biologists. The success of PCR workflows is highly dependent on the quantity, purity, and degree of fragmentation of the DNA. Here, Bertin’s top scientists have presented examples of optimized homogenization protocols to obtain high quality nucleic acids and guarantee the success of your PCR workflow.