DNA & RNA Purification
Optimized for a variety of applications requiring larger per well volume processing. Plates are constructed of chemicallyresistant, biologically-inert polypropylene.
AcroPrep™ 384-well Filter Plates are ideal for use in high volume, high throughput sample prep applications. Plates are constructed from chemically-resistant, biologically-inert polypropylene with a clear polystyrene lid.
AcroPrep™ Advance 96-Well Filter Plates for Ultrafiltration provide rapid, efficient separation of biomolecules. Omega™ membrane provides high recovery and typically results in > 90% recovery of target biomolecules.
The AcroPrep™ advance 96-well long tip filter plate for Nucleic Acid Binding (NAB plate) incorporates a silica-based quartz glass fiber media to allow for efficient binding of DNA and RNA, while providing smooth flow and rapid processing of samples.
AcroPrep™ Advance Filter Plates for Lysate Clearance are manufactured with biologically inert materials that allow clarification of most types of lysates without loss of target molecules.
Microsep™ Advance centrifugal filters provide precise, quick recovery of microliter volumes. Achieve 50X concentration and > 90% recovery in just minutes.
Particulate removal for longer HPLC and UHPLC column life. High spin speed and larger EFA reduces spin times. For samples from 3 - 20 mL.
Macrosep® Advance centrifugal filters quickly concentrate up to 20 mL of biological samples. Rapidly concentrates 20 mL sample volumes to 0.5 mL. Provides high recoveries, typically > 90%.
Use Nanosep® devices to concentrate, purify, and desalt peptides, proteins, oligonucleotides, DNA, and RNA. Available with low proteinbinding Omega™, Bio-Inert®, and wwPTFE membranes.
Provide high sensitivity and low background for enhanced detection and resolution. Will not crack, shrink, or tear when subjected to multiple cycles of hybridization, stripping, and reprobing.
Membranes have a high binding affinity (209µg/cm2) and are ideal for Western blot confirmatory tests. High binding capacity for proteins and nucleic acids. Lower protein burnthrough than competitors in electrophoretic transfers.
