Cresivis 96-well parallel dialysis plate

High-throughput dialysis and sample processing

High-throughput dialysis and automated sample processing

Cresivis develops a parallel processing platform for microsample dialysis, buffer exchange, and process-condition screening. Built around familiar 96-well workflows, it helps R&D teams move from one-tube operations to validated, repeatable plate-based processes.

Core product
96-well parallel dialysis plate (96W-D-ST)
Working volume per well
50–250 μL / 50–400 μL
Membrane and MWCO
Regenerated cellulose (RC), standard 12 kDa
Typical uses
Buffer exchange, desalting, ethanol removal, and formulation screening

Platform focus

Designed around real laboratory workflows—from dialysis architecture and handling to application validation.

Parallel processing

Dialysis and sample-processing units built around a 96-well interface for simultaneous evaluation of multiple samples and conditions.

Lab-friendly workflow

Open loading, sampling, and plate-array conventions reduce the transition cost from familiar pipetting workflows.

Configurable validation

Architecture and application testing are configured around sample volume, membrane specification, dialysis conditions, and analytical endpoints.

Cresivis 96-well parallel dialysis plate, model 96W-D-ST-25

Featured product

96-well parallel dialysis plate

Open wells on top are loaded and sampled exactly like an ordinary 96-well plate, while an independent regenerated-cellulose tubular membrane beneath each well immerses its active section in the dialysate. Fluid paths are isolated well to well, with CV < 5% across an overnight dialysis. A 25 mm membrane gives 50–250 μL per well; 35 mm gives 50–400 μL.

  • Ethanol removal and buffer exchange for LNP and nucleic-acid delivery systems
  • Desalting and buffer exchange for proteins, peptides, and low-volume biological samples
  • Parallel process development and method comparison across formulations and conditions
  • Localized alternatives to imported microdialysis plates with application-specific validation

Collaboration

Start with the application goal, then define the architecture, materials, and validation boundaries.

01

Define sample volume, target removals, and recovery requirements

02

Select the model, MWCO, membrane length, companion container, and dialysate conditions

03

Run recovery and leakage pilots, review the data, and confirm the specification