Waters - Oligonucleotide Columns
Manufactured by Waters
Scaleable Column Offerings
Oligonucleotide columns contain second-generation hybrid silica BEH Technology particles functionalized with C18. The separation of detritylatedsynthetic oligonucleotide samples is based on the well-established method of ion-pair, reversed-phase chromatography. The availability of 1.7 Μm UPLC particles or 2.5 Μm HPLC/UHPLC particles in various column dimensions provides flexibility to meet various lab-scale isolation or analysis needs and delivers exceptional sample resolution and superior column life.
In addition, Waters manufacturing and quality control testing procedures help ensure consistent batch-to-batch and column-to-column performance regardless of application demands.
In addition, Waters manufacturing and quality control testing procedures help ensure consistent batch-to-batch and column-to-column performance regardless of application demands.
Active Questions & AnswersAsk a Question
There are no current Discussions
HPLC Columns Service ProvidersView All (22)
Documents & Manuals
There are no Documents or Manuals available.
Features of Oligonucleotide Columns
Exceptional Resolution of Oligonucleotide Mixtures
ACQUITY UPLC Oligonucleotide C18, 1.7 Μm (designed for use with an ACQUITY UPLC System) and XBridge Oligonucleotide C18, 2.5 Μm Columns are well suited for the analysis of detritylated oligonucleotides using ion-pair, reversed-phase chromatography.
Outstanding Column Life
Oligonucleotide columns packed with BEH Technology particles have shown remarkable column longevity, under these demanding separation conditions, while maintaining outstanding separation performance.
Synthetic Oligonucleotide and DNA/RNA Species
Ion-pairing reversed phase (IP-RP) liquid chromatography is a commonly accepted separation strategy for the analysis and purification of detritylated oligonucleotides. The ion-pairing additive in the mobile phase is adsorbed on a hydrophobic C18 sorbent and provides for charge-to-charge interactions with negative charges contained on the oligonucleotide backbone (i.e., phosphate groups).
As a result, an efficient charge-based (length-based) oligonucleotide separation is achieved. Gradient elution using an acetonitrile or methanol eluent displaces both ion-pairing agent and the oligonucleotides from the sorbent surface while separation selectivity and resolution decreases with increasing oligonucleotide length making the separation of long oligonucleotides challenging.
Oligonucleotide Standards
The pre-packaged MassPREP Oligonucleotide Standard is designed for verification of HPLC/UPLC instruments and column performance for analysis of synthetic oligonucleotides.
Oligonucleotide Desalting by Solid-Phase Extraction
Desalting of synthetic oligonucleotides is essential for MS analysis (QC, genotyping applications and SNP analysis). The Oasis ΜElution Plate combines patented plate design, proven Oasis chemistries, and generic protocols enabling elution volumes as low as 25 ΜL. You can perform SPE clean-up and concentration of very small sample volumes. The Oasis Hydrophilic-lipophilic-balanced (HLB) sample extraction products incorporate a patented copolymer made from a balanced ratio of two monomers; the lipophilic divinylbenzene and the hydrophilic N-vinylpyrolodone.
General Specifications
There are no General Specifications available.
