Owl™ Sequencing System Spacer Sets and Glass Plates Offset Glass;

Catalog nr. S2S43G
Thermo Scientific - Equipment LED

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Sale price€27,60
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Description

Owl™ Sequencing System offset glass plate is a dedicated glass plate accessory designed for use with Owl™ Sequencing Gel Casting Systems in molecular biology and sequencing laboratories. The offset glass measures 43 cm in length by 35 cm in width and has a thickness of 0,18 in, giving a stable, precisely sized surface for sequencing gel casting. It forms part of the Owl™ Sequencing System spacer sets and glass plates portfolio and is intended for Thermo Scientific sequencing gel casting systems. When paired with the matching spacers and system hardware, the plate supports reproducible gel preparation for DNA sequencing electrophoresis and related separation workflows. The offset configuration helps establish the correct geometry during casting so that gels form evenly across the plate area. Supplied as a single piece from manufacturer Thermo Scientific - Equipment LED, this glass plate is a practical replacement or expansion component for laboratories already equipped with Owl™ sequencing instrumentation and seeking consistent casting performance in routine sequencing applications.

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

Key features

  • Pack size: 1 pc
  • Type: Offset glass plate
  • Dimensions: 43 cm L × 35 cm W × 0,18 in thickness
  • Brand: Owl™
  • Compatible with: Owl™ Sequencing Gel Casting Systems

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Questions about Owl™ Sequencing System Spacer Sets and Glass Plates Offset Glass;

What is this article?

Owl™ Sequencing System Spacer Sets and Glass Plates Offset Glass; 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 Microbiology lab supplies.

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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