Pular para o conteúdo
Merck
Todas as fotos(1)

Documentos

11888412001

Roche

PCR Nucleotide MixPLUS

solution, Roche, pkg of 2 × 100 μL (10 mM each), suitable for RT-PCR

Sinônimo(s):

PCR | Nucleotide

Faça loginpara ver os preços organizacionais e de contrato


About This Item

Código UNSPSC:
41116100

forma

solution

Nível de qualidade

uso

sufficient for 500 reactions

embalagem

pkg of 2 × 100 μL (10 mM each)

fabricante/nome comercial

Roche

técnica(s)

RT-PCR: suitable

cor

colorless

solubilidade

water: miscible

temperatura de armazenamento

−20°C

Descrição geral

PCR Nucleotide MixPLUS is a clear, colorless solution of the sodium salts of dATP, dCTP, dGTP, each at a concentration of 10 mM, and dUTP at a concentration of 30 mM in Water, PCR Grade. This nucleotide mixture can be added directly to polymerase chain reactions.
The incorporation of dUTP in place of dTTP allows the degradation of contaminating PCR products from former reactions with Uracil-DNA Glycosylase (UNG) to prevent carryover contamination from previous amplifications.

Aplicação

  • This ready-to-use nucleotide mix is a premixed solution of the sodium salts of dATP, dGTP, and dCTP, each at a concentration of 10 mM, and dUTP at a concentration of 30 mM in water. This mix is optimized for use in all types of amplification reactions: PCR
  • RT-PCR
  • Prevention of carryover contamination
To allow decontamination of PCR or RT-PCR, dUTP in place of dTTP is incorporated into the PCR product. Subsequent reactions may then be treated with Uracil-DNA Glycosylase (UNG). Avoiding the need of re-opening the reaction vial, the vials are incubated at +20 °C, resulting in the degradation of potentially contaminating uracil-containing amplification products. During this step, template DNA and RNA remain unaffected, since normal DNA does not contain uracil, and RNA does not serve as a substrate for UNG. Before starting the actual thermocycling program, UNG is inactivated by incubation at +95 °C. Uracil -DNA Glycosylase, heat-labile is particularily useful, as it is fully inactivated already after incubation at +95 °C for 2 minutes. The natural enzyme from E. coli requires incubating the reaction mixture for 10 minutes at +95 °C. The shorter heat treatment substantially reduces the risk for loosing the template nucleic acid, which typically is present at low concentrations only. This is of particular importance, when performing RT-PCR. We therefore recommend the use of Uracil-DNA Glycosylase.
It has been used in LightCycler PCR assay to identify B. pertussis and B.parapertussis in nasopharyngeal swabs. It has also been used in quantitative PCR (qPCR) assay.

Características e benefícios

The PCR Nucleotide MixPLUS can be added directly to amplification reactions.PCR Grade nucleotides from Roche are specially manufactured and purified to the highest possible chemical purity. They can be used to amplify even low amounts of template RNA and DNA.
Improve yield and performance
  • Choose a convenient ready-to-use mix of all 4 nucleotides.
  • Achieve the highest PCR and RT-PCR sensitivity.
  • Insist on highest purity (>99%) nucleotides

Embalagem

1 set containing 4 ready-to-use mixes

Qualidade

Function tested in PCR to ensure specific DNA amplification. Decontamination with UNG is verified. No RNases or DNases are detectable according to the current Quality Control procedures.

Outras notas

For life science research only. Not for use in diagnostic procedures.

Somente componentes do kit

Nº do produto
Descrição

  • dATP, PCR Grade, sodium salt 10 mM

  • dCTP, PCR Grade, sodium salt 10 mM

  • dGTP, PCR Grade, sodium salt 10 mM

  • dUTP, PCR Grade, sodium salt 10 mM

Código de classe de armazenamento

12 - Non Combustible Liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

does not flash

Ponto de fulgor (°C)

does not flash


Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Lynne M Sloan et al.
Journal of clinical microbiology, 40(1), 96-100 (2002-01-05)
A rapid real-time multiplex PCR assay for detecting and differentiating Bordetella pertussis and Bordetella parapertussis in nasopharyngeal swabs was developed. This assay (LC-PCR-IS) targets the insertion sequences IS481 and IS1001 of B. pertussis and B. parapertussis, respectively, and is performed
Miki Kasai et al.
Journal of clinical microbiology, 46(11), 3690-3702 (2008-10-11)
We developed two real-time quantitative PCR (qPCR) assays, targeting the 28S rRNA gene, for the diagnosis of zygomycosis caused by the most common, clinically significant Zygomycetes. The amplicons of the first qPCR assay (qPCR-1) from Rhizopus, Mucor, and Rhizomucor species

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica