11888412001
Roche
PCR Nucleotide MixPLUS
solution, Roche, pkg of 2 × 100 μL (10 mM each), suitable for RT-PCR
Synonyme(s) :
PCR | Nucleotide
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About This Item
Produits recommandés
Forme
solution
Niveau de qualité
Utilisation
sufficient for 500 reactions
Conditionnement
pkg of 2 × 100 μL (10 mM each)
Fabricant/nom de marque
Roche
Technique(s)
RT-PCR: suitable
Couleur
colorless
Solubilité
water: miscible
Température de stockage
−20°C
Catégories apparentées
Description générale
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.
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.
Application
- 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
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.
Caractéristiques et avantages
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
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
Conditionnement
1 set containing 4 ready-to-use mixes
Qualité
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.
Autres remarques
For life science research only. Not for use in diagnostic procedures.
Composants de kit seuls
Réf. du produit
Description
- 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
Code de la classe de stockage
12 - Non Combustible Liquids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
does not flash
Point d'éclair (°C)
does not flash
Certificats d'analyse (COA)
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Les clients ont également consulté
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
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
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