ROTI®Mix PCR 3, 10 mM (each dNTP), 40 mM (total), 0.2 ml, plastic

Catalog nr. L785.1
Carl Roth

Volume: 0.2 ml
Value Packs: 1 piece
Price:
Sale price€33,90

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Description

ROTI®Mix PCR 3 is a ready-to-use deoxynucleotide mix for PCR and related DNA/RNA analysis workflows in molecular biology. Each dNTP—dATP, dTTP, dGTP and dCTP—is present at 10 mM, giving a total nucleotide concentration of 40 mM in a balanced formulation suited to amplification setups. The premixed composition reduces pipetting steps and helps maintain consistent nucleotide ratios across reactions, supporting reproducible PCR performance in research laboratories. This mix from manufacturer Carl ROTH fits standard molecular-biology protocols where defined dNTP input is required for DNA amplification and related nucleic-acid work. Ready-to-use presentation simplifies reaction assembly and limits handling of individual nucleotide stocks. Laboratories engaged in life-science and molecular diagnostics-oriented PCR can incorporate ROTI®Mix PCR 3 as a convenient nucleotide component within established thermal-cycling procedures, benefiting from clear concentration specification and a format aligned with routine bench practice in DNA and RNA analysis.

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

Key features

  • Pack sizes: 0.2 ml, 1 ml, 5 ml
  • Storage temperature: −20 °C
  • Concentration: 10 mM (each dNTP)
  • Total concentration: 40 mM
  • Composition: dATP, dTTP, dGTP, dCTP
  • Technical Information Sheet: PDF
  • Safety Data Sheet: PDF

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Questions about ROTI®Mix PCR 3, 10 mM (each dNTP), 40 mM (total), 0.2 ml, plastic

What is this article?

ROTI®Mix PCR 3, 10 mM (each dNTP), 40 mM (total), 0.2 ml, 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 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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The technical information on this page is the manufacturer's sheet. Read that, not a rewritten specification.

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