[Improved performance] Chromatographic purification of pDNA is often a bottleneck due to low dynamic binding capacities (DBC), pDNA recovery and/or low selectivity of columns. 𝐇𝐨𝐰 𝐜𝐚𝐧 𝐰𝐞 𝐢𝐧𝐜𝐫𝐞𝐚𝐬𝐞 𝐃𝐁𝐂? 🔎 The goal of our investigation was to increase the DBC for pDNA on a monolith stationary phase by grafting the surface with linear polymethacrylate brushes, while retaining high pDNA recovery and chromatographic selectivity between pDNA and RNA impurities. 𝐔𝐩 𝐭𝐨 8-𝐭𝐢𝐦𝐞𝐬 𝐥𝐚𝐫𝐠𝐞𝐫 𝐃𝐁𝐂 Dynamic binding capacities for 7.3 kpb pDNA were up to 8-times larger compared to non-grafted CIMmultus 1 ml columns. And that’s not all … read on: https://lnkd.in/dHmgrGxy #pDNA #chromatography #RNA #purification #biotech
I am impressed by this talented team to finally develop monoliths beyond the current already excellent capacity levels.
Impressing and Congratulation! Greetings from Vienna Cornelia
Wuxi Extpure Solutions Co.,Ltd - CEO
10hwonderful work,one qiestion:it bring more blocking risk