Owl™ SGC Sequencing Gel Casters 71cm Each

Catalog nr. SGC1
Thermo Scientific - Equipment LED

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Prix réduit€427,00
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Description

Owl™ SGC sequencing gel caster enables bubble-free sequencing gels to be cast in less than three minutes without taping or special assembly steps. The adjustable casting platform accommodates glass plates from 20 to 42 cm wide and is supplied with width-adjustment knobs and twelve binder clamps for secure plate positioning. Overall dimensions are 71 × 21 × 12,2 cm (28 × 8,25 × 4,75 in), giving a stable footprint for sequencing-gel preparation. By simplifying the casting process, exposure to hazardous acrylamide is reduced and cleanup time is shortened. Designed for use with the Owl™ SGC sequencing system, this caster from manufacturer Thermo Scientific supports efficient preparation of large-format sequencing gels in molecular-biology and genomics laboratories. Supplied as one complete unit ready for integration into existing Owl™ SGC workflows.

This article is part of PCR, qPCR & nucleic acid analysis reagents, in Molecular biology.

Key features

  • Pack size: 1 pc
  • Type: Sequencing gel caster
  • Overall length: 71 cm
  • Overall width: 21 cm
  • Overall height: 12,2 cm
  • Glass plate width range: 20 to 42 cm

Besoin d'une assistance technique ?

info@luminixhealth.com +32 13 30 43 61

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Questions about Owl™ SGC Sequencing Gel Casters 71cm Each

What is this article?

Owl™ SGC Sequencing Gel Casters 71cm Each is the article on this page. Luminix Health distributes Thermo Scientific - Equipment LED for laboratory use. It sits in PCR, qPCR & nucleic acid analysis reagents, inside Molecular biology, in Milieux microbiologiques.

PCR and qPCR reagents are the polymerase, the nucleotides, the buffer and often a ready master mix, plus the dyes a real-time instrument reads. Hot-start enzymes and proofreading enzymes are different tools. A master mix already contains nucleotides. Adding them again is a failed reaction.

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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