Description
Receiver plate 50 µm hydrophilized is a 96-well laboratory plate fitted with inserted hydrophilized filter frits of 50 µm pore size for controlled liquid handling in multiwell workflows. The hydrophilized frits support reliable wetting and passage of aqueous samples, making the plates suitable for gravity flow, centrifugation, and vacuum-driven processing on standard manifolds and rotors. Each plate integrates the filter elements directly into the 96-well format, so laboratories can run parallel filtration or collection steps without separate frit assembly. Offered as a pack of four plates from manufacturer Macherey-Nagel, this consumable fits biochromatography and sample-preparation routines where consistent pore geometry and multiwell throughput are required. The 50 µm frit specification helps retain particulate material while allowing clarified liquids to pass under gravity, spin, or vacuum conditions. Use these receiver plates as collection or intermediate vessels in high-throughput filtration sequences, buffer exchange support steps, or other parallel protocols that benefit from a defined hydrophilized frit interface across all wells of the plate.
This article is part of Sorbents, silica gel & ion exchangers, in SPE & sample preparation.
Key features
- Pack size: 4 pc(s)
- Product type: 96-well receiver plates
- Pore size: 50 µm
- Filter medium: hydrophilized filter frits
- Process modes: gravity flow, centrifugation, vacuum
- EAN: 4046681158377
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Questions about Receiver Plate 50 µm hydrophilized (4)
What is this article?
Receiver Plate 50 µm hydrophilized (4) is the article on this page. Luminix Health distributes Macherey-Nagel for laboratory use. It sits in Sorbents, silica gel & ion exchangers, inside SPE & sample preparation, in Chromatography equipment.
Loose sorbent, silica gel and ion-exchange resin are the phases bought in bulk to pack a column or to stir into a solution. Particle size and activity, or the ion-exchange capacity, are the specification. A TLC silica and a flash silica of different particle sizes are not the same separation.
Solid-phase extraction holds a compound on a sorbent while the rest of the sample is washed away, then releases it in a small volume. The sorbent, the bed mass and the solvents are the method. Silica, ion exchangers and polymer phases do different jobs. A flash column is the same idea scaled toward purification rather than trace cleanup. The molecules are on PubChem, named by IUPAC.
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