AcroPrep 24-Well Filter Plate w/ Omega Membrane- 30kDa, 8/Pk
Pall SKU: 97055

AcroPrep Polyethersulfone (PES) Filter Plate, 30 kDa MWCO, 8/Pk - 97055

Filter plates clarify withdrawn samples across a multi-well format, delivering analysis-ready aliquots in parallel throughout an automated sampling run. PES stays stable across the full pH 1 to 14 range and accepts water-based reagents without preconditioning. Clarified aliquots keep particulate load off the analytical column and detector, extending instrument uptime across a full plate of samples.

Key Characteristics

• Low protein binding preserves dilute analytes for maximum recovery
• Broad compatibility with aqueous buffers, aliphatic alcohols, glycols, and strong bases
• High flow rate with low extractable background for clean preparations
• Stable across the full pH 1 to 14 operating range
• Naturally hydrophilic surface wets without pre-wetting in aqueous applications

Reproducible separations start with samples that reach the column free of particulates. Pre-injection filtration protects the resolution your methods depend on across your chromatography methods. Reach out to the Tisch Scientific team for application support, volume pricing, and technical assistance with your filtration product selection.

Capacity

7mL

Material

Polyethersulfone (PES)

MWCO(Da)

30k

Sterility

Sterile

Wettability

Hydrophilic

• Analytical Sample Prep - Turbid samples reduce to clean, injection-ready fractions for reproducible chromatographic and spectroscopic assays.
• Unattended Sampling Runs - Single-use plates paired with automated instruments enable clean, hands-off sample collection through a full test.
• Column Protection - Particulate removal before injection guards analytical columns and detectors from fouling and stretches maintenance intervals.
• High-Throughput Cleanup - Plate-based clarification prepares large analytical batches in parallel and cuts hands-on preparation time per sample.
• 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.