Acidic anion exchange selectively captures extracellular DNA while limiting RNA and vesicle binding, enabling clean sequential fractions.
Surface presentation in eukaryotic cell display predicts polypeptide solubility and non-specific binding for earlier developability screening.
Blocking DNA-PKcs and 53BP1 suppresses NHEJ, boosts HDR knock-in efficiency, and improves cell viability during gene editing.
Automated RCA DNA production combines protein removal, anion exchange purification, and inline monitoring in a closed workflow for on-site use.
Oppositely charged particle coatings capture analytes, then break down to release them under mild conditions without desalting before analysis.
A two-part chemical bait captures total nucleic acids on non-silica substrates while reducing non-specific binding and false positives.
Multiple cleavage sites break the plasmid backbone into small fragments, enabling faster insert purification with higher yield and purity.
Tagmentation inserts sequencing primers into barcoded mRNA hybrids, cutting single-cell library prep time and reagent use.