NucleoSpin 96 RNA Filter Plate (4)

Catalog nr. 740711
Macherey-Nagel

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Sale price€275,99
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Description

NucleoSpin 96 RNA Filter Plate (4) comprises 96-well filter plates intended for filtration of cell and tissue homogenates prior to or within RNA isolation workflows. The multiwell layout enables simultaneous clarification of many samples, helping remove debris and particulate material from lysates in a structured plate format. Delivered as a pack of four plates, the set supports repeated filtration runs in medium- to high-throughput molecular biology settings. These filter plates from manufacturer Macherey-Nagel are positioned for use alongside NucleoSpin RNA plate systems where homogenate filtration is a defined process step. Laboratories working with cultured cells or tissue samples can apply the plates to prepare clearer lysates before binding and purification stages. The pack has a net weight of 0,50 kg and a compact footprint suited to standard laboratory storage. As dedicated filtration consumables, they provide a practical option for biochromatography and nucleic acid preparation benches that standardise on 96-well processing rather than individual spin columns.

This article is part of DNA & RNA extraction kits, in Molecular biology.

Key features

  • Pack size: 4 pc(s)
  • Product type: 96-well RNA filter plates
  • Format: 96-well plates
  • EAN: 4046681158148

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Questions about NucleoSpin 96 RNA Filter Plate (4)

What is this article?

NucleoSpin 96 RNA Filter Plate (4) is the article on this page. Luminix Health distributes Macherey-Nagel for laboratory use. It sits in DNA & RNA extraction kits, inside Molecular biology, in Life Science & Microbiology.

An extraction kit lyses the sample and then binds the nucleic acid, usually on a column or on a bead, and washes the rest away. Kits for blood, tissue, soil or a PCR cleanup are different chemistries. Yield and the size of fragments they keep are in the protocol. An RNA kit has to protect against RNase.

Molecular biology here is the handling of DNA and RNA. Extraction kits break the cell and then separate the nucleic acid from protein and from the other nucleic acid. PCR and qPCR reagents copy a chosen sequence so it can be seen. The enzymes and the nucleotides are what the copy depends on. Nuclease contamination destroys the sample before the kit can save it. Sequences are on NCBI Nucleotide. Papers are on PubMed.

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