The analysis of mineral and additional trace metal screening of medicinal and recreational cannabis, as well as related products, provides key labeling information. The analysis can be carried out at all stages of production to ensure product quality control and products that are free of toxic metals.

Setting up live cell experiments can be challenging, as temperature, CO2 and evaporation need to be carefully controlled to ensure optimal cell growth conditions.

The synthesis of active pharmaceutical ingredients (API) may require multiple reaction steps that produce undesirable reaction byproducts or utilize various solvents that have to be removed from the finished product.

The purity of oligonucleotide preparations produced by solid-phase synthesis can be very high. However, purification is often required to remove incomplete or erroneous sequences.

Whether you’re investing in your first digital imaging system for gel and membrane imaging, upgrading existing equipment, or just going with what’s already installed in your laboratory, you’ll need to understand key technical specifications to get the most out of your imager.

Standard ELISA techniques for detecting protein biomarkers in serum or other biological samples can leave you with sensitivity that doesn’t quite cut it, analyte cross-reactivity, and reproducibility that’s ok at best.

Fragment-based drug design has become an increasingly popular platform for the identification of lead candidates in drug discovery programs.

One of the most in-demand workflows any food and environmental lab is a solid method for the analysis of polar pesticides. Here we present a collaborative method with Nofalab, Laboratories, Netherlands.

A new era of high sensitivity therapeutic quantitation is here with lower flows and lower hassles.

In biologics development your timelines are tight, the pressure is on and mistakes can be costly.