Investigating the Power of Selectivity in Low Flow Separations – Opening New Doors
June 28th 2021Monday, June 28, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST The goal of any chromatographic separation is the resolution of different analyte peaks from those with similar elution profiles. Join us to learn the three critical factors that govern the resolution of a critical pair.
Comparing Performance of High-Throughput, Trityl-on RNA/DNA Purification Products v2
June 23rd 2021Clarity QSP provides an alternative trityl-on approach for separating truncated sequences and synthetic contaminants from the protected full-length sequence. By incorporating a polymeric sorbent with a unique buffer formula, aborted fragments and synthetic contaminants are removed during sample loading offering a departure from the traditional RPC mechanism. Multiple buffers and gradient elutions are eliminated, thereby making Clarity QSP a 3-step product for trityl-on oligonucleotide purification.
Avoiding Depurination During Trityl-on Purification v2
June 23rd 2021Trityl-on methodologies for the analysis of crude synthetic oligonucleotides has many benefits however depurination during trityl-on methodologies can lead to nucleic acid damage. This technical note explores a new trityl-on procedure that minimizes the risk of depurination.
Method Development Strategies for Purity Analysis of Proteins by Intact and Subunit Analysis
May 24th 2021***Live: Monday, May 24, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** Join us to learn best practices in method development for intact and subunit purity analysis for mAbs by reversed-phase liquid chromatography (RPLC), including how to best adjust method parameters such as temperature, gradient slope, and flow rate to obtain high-quality impurity profiling and ensure method robustness and reproducibility. ***On Demand until May 24, 2022***