AcroPrep Depth Media / PES Filter Plate, 0.2 µm, 8/Pk - 97026
Withdrawn media carries undissolved particulates into the analytical flow path, and the plate clears that load before injection to protect the instrument. PES minimizes protein binding to maximize sample and analyte recovery while achieving sterile-grade retention with high recovery and accepts water-based reagents without preconditioning. Analysis-ready fractions move directly to chromatographic or spectroscopic measurement, shortening the path from sample collection to reportable result.
Key Characteristics
- Naturally hydrophilic surface wets without pre-wetting in aqueous applications
- Low protein binding preserves dilute analytes for maximum recovery
- High flow rate with low extractable background for clean preparations
- Broad compatibility with aqueous buffers, aliphatic alcohols, glycols, and strong bases
- Absolute pore size rating gives consistent results across protocols
Sample clarification before injection is the cheapest insurance your chromatography system has. Pre-injection filtration protects the resolution your methods depend on across your chromatography methods. Ask the Tisch Scientific team about blanket-order pricing and quality documentation for your routine filtration needs.
- Capacity
- 7mL
- Pore Size (µm)
- 0.2
- Sterility
- Sterile
- Wettability
- Hydrophilic
- High-Throughput Cleanup - Plate-based clarification prepares large analytical batches in parallel and cuts hands-on preparation time per sample.
- Automated Dissolution Sampling - Filtered aliquots pulled from dissolution vessels arrive analysis-ready with no manual clarification step.
- Column Protection - Particulate removal before injection guards analytical columns and detectors from fouling and stretches maintenance intervals.
- Pre-Chromatography Clarification - Clarified aliquots reach the autosampler free of particulates, protecting column lifetime across long runs.
- Parallel Sample Processing - Multiple vessel samples clarify at once, tightening run-to-run consistency across a full analytical sequence.
- Pharmaceutical Release Testing - Clarified samples meet USP, EP, and JP method requirements for routine QC and batch release workflows.