pBR328 Mix I, DNA-marker (lyophil.), 50 µg, plastic

Catalog nr. T146.1
Carl Roth

Volume: 50 µg
Value Packs: 1 piece
Price:
Sale price€104,85
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Description

pBR328 Mix I is a lyophilised DNA marker supplied with gel loading buffer for nucleic acid electrophoresis. The preparation is not pre-dyed, giving laboratories full flexibility to apply their preferred stain or dye system when visualising fragment patterns on agarose or polyacrylamide gels. Intended for routine size estimation and gel calibration in molecular biology workflows, this marker supports clear band resolution across typical pBR328-derived fragment sets used in cloning and restriction analysis. Each unit provides 50 µg of material in a convenient plastic pack, suited to repeated use in research and teaching laboratories. The lyophilised format aids stable handling prior to reconstitution according to standard laboratory practice. Offered from manufacturer Carl ROTH within the DNA markers range for life-science electrophoresis, pBR328 Mix I integrates readily into existing gel-loading protocols without requiring a pre-coloured ladder. Use it wherever a reliable, undyed DNA size standard with accompanying loading buffer is needed for reproducible fragment comparison and documentation.

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

Key features

  • Pack size: 50 µg plastic
  • Product type: DNA marker (lyophilised)
  • Includes: gel loading buffer
  • Dye status: not pre-dyed
  • Technical Information Sheet: PDF
  • Safety Data Sheet: PDF

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Questions about pBR328 Mix I, DNA-marker (lyophil.), 50 µg, plastic

What is this article?

pBR328 Mix I, DNA-marker (lyophil.), 50 µg, plastic is the article on this page. Luminix Health distributes Carl Roth for laboratory use. It sits in PCR, qPCR & nucleic acid analysis reagents, inside Molecular biology, in Life Science & Microbiology.

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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What should I check before I order?

The technical information on this page is the manufacturer's sheet. Read that, not a rewritten specification.

When this page shows a safety data sheet, use that manufacturer file. Hazard text does not belong in the sales description. For a pack size, a grade or a certificate that is not on the page, send a quote request or contact the team.

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