11888412001
Roche
PCR Nucleotide MixPLUS
solution, Roche, pkg of 2 × 100 μL (10 mM each), suitable for RT-PCR
Synonym(s):
PCR | Nucleotide
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About This Item
Recommended Products
form
solution
Quality Level
usage
sufficient for 500 reactions
packaging
pkg of 2 × 100 μL (10 mM each)
manufacturer/tradename
Roche
technique(s)
RT-PCR: suitable
color
colorless
solubility
water: miscible
storage temp.
−20°C
Related Categories
General description
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.
Features and Benefits
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
Packaging
1 set containing 4 ready-to-use mixes
Quality
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.
Other Notes
For life science research only. Not for use in diagnostic procedures.
Kit Components Only
Product No.
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
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 1
flash_point_f
does not flash
flash_point_c
does not flash
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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
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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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