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Taq DNA Polymerase

Taq DNA Polymerase

Taq polymerase is a thermostable DNA polymerase

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FLUXERGY SARS-CoV-2 PCR Kit

Test type: T-PCR, direct Time to result: ~ 60 minutes Sample preparation: ~ 3 min from reagent thaw, no extraction required Sample Type: NPS in

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The behaviour of 5-hydroxymethylcytosine in bisulfite sequencing.

The behaviour of 5-hydroxymethylcytosine in bisulfite sequencing.

CONTEXT We have recently shown that the tet family enzymes convert 5-™ 5-hydroxymethylcytosin (5-HMC) to DNA. 5-HMC is present at high levels in embryonic stem

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A simple method for site-directed mutagenesis using the polymerase chain reaction.

A simple method for site-directed mutagenesis using the polymerase chain reaction.

We have developed a general and simple method for directing specific sequence modifications in a plasmid using the amplification approved by the reaction of the

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Rapid detection and quantification of RNA of Ebola and Marburg viruses, Lassa virus, Crimean-Congo hemorrhagic fever virus, Rift Valley fever virus, dengue virus, and yellow fever virus by real-time reverse transcription-PCR.

Rapid detection and quantification of RNA of Ebola and Marburg viruses, Lassa virus, Crimean-Congo hemorrhagic fever virus, Rift Valley fever virus, dengue virus, and yellow fever virus by real-time reverse transcription-PCR.

Viral hemorrhagic fevers (VHFS) are acute infections with high mortality rates. Significant VHF agents are Ebola and Marburg viruses (MBGV / EBOV), Lassa Virus (LASV),

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High fidelity amplification using a thermostable DNA Pyrococcus Furiosus isolated polymerase.

High fidelity amplification using a thermostable DNA Pyrococcus Furiosus isolated polymerase.

A polymerase thermostable DNA which has an associated exonuclease activity has been isolated from the hyperthermophilic archaebacterium, Pyrococcus Furiosus (PFU). To test its loyalty, we

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Contamination and sensitivity issues with a real-time universal 16S rRNA PCR.

Contamination and sensitivity issues with a real-time universal 16S rRNA PCR.

A set of universal oligonucleotide primers for the retained regions of the eubactterial gene 16S arrnes has been designed for use with the 7700 Real-Time

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CONTRIBUTION OF ERRORS INDUCED BY THE TAQ POLYMERASE TO ESTIMATE THE DIVERSITY OF RNA VIRUS.

CONTRIBUTION OF ERRORS INDUCED BY THE TAQ POLYMERASE TO ESTIMATE THE DIVERSITY OF RNA VIRUS.

The genetic diversity of a vesicular stomatitis virus population was analyzed by RT-PCR, cloning and sequencing of about 500 nucleotide regions of the virus genome.

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Taq DNA Polymerase Mutants and 2′-Modified Sugar Recognition.

Taq DNA Polymerase Mutants and 2′-Modified Sugar Recognition.

chemical modifications to DNA, such as modification 2 ‘, is expected to increase the utility of DNA biotechnology; However, other forms of modification of DNA

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Obstacles of Multiplex Real-Time PCR for Bacterial 16S rDNA: Primer Specifity and DNA Decontamination of Taq Polymerase.

Obstacles of Multiplex Real-Time PCR for Bacterial 16S rDNA: Primer Specifity and DNA Decontamination of Taq Polymerase.

BACKGROUND: Detection of bacteria by PCR applied for screening blood and blood products with special attention platelet concentrates. For practical use is expected that the

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Fusion of Taq DNA polymerase with single-stranded DNA binding-like protein of Nanoarchaeum equitans-Expression and characterization.

Fusion of Taq DNA polymerase with single-stranded DNA binding-like protein of Nanoarchaeum equitans-Expression and characterization.

DNA polymerases are present in all organisms and enzymes important that synthesize DNA molecules. They are used in various fields of science, especially as an

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Recent Posts

  • FLUXERGY SARS-CoV-2 PCR Kit
  • The behaviour of 5-hydroxymethylcytosine in bisulfite sequencing.
  • A simple method for site-directed mutagenesis using the polymerase chain reaction.
  • Rapid detection and quantification of RNA of Ebola and Marburg viruses, Lassa virus, Crimean-Congo hemorrhagic fever virus, Rift Valley fever virus, dengue virus, and yellow fever virus by real-time reverse transcription-PCR.
  • High fidelity amplification using a thermostable DNA Pyrococcus Furiosus isolated polymerase.

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Categories

  • Antibodies
  • Assay Kits
  • Biology Cells
  • Blog
  • cDNA
  • Clia Kits
  • Culture Cells
  • Devices
  • DNA
  • DNA Templates
  • DNA Testing
  • Elisa Kits
  • Enzymes
  • Equipments
  • Exosomes
  • Gels
  • Isotypes
  • Medium & Serums
  • NATtrol
  • Panel
  • Particles
  • PCR
  • Pcr Kits
  • Peptides
  • Reagents
  • Recombinant Proteins
  • Ria Kits
  • RNA
  • Test Kits
  • Vector & Virus
  • Western Blot

Recent Posts

  • FLUXERGY SARS-CoV-2 PCR Kit
  • The behaviour of 5-hydroxymethylcytosine in bisulfite sequencing.
  • A simple method for site-directed mutagenesis using the polymerase chain reaction.
  • Rapid detection and quantification of RNA of Ebola and Marburg viruses, Lassa virus, Crimean-Congo hemorrhagic fever virus, Rift Valley fever virus, dengue virus, and yellow fever virus by real-time reverse transcription-PCR.
  • High fidelity amplification using a thermostable DNA Pyrococcus Furiosus isolated polymerase.

Tags

cdna 260/280 cdna amd cdna avm cdna cds cdna def cdna definition cdna degradation cdna from mrna cdna gel cdna gpu cdna lab cdna nyc dnajlion7 dnajlion7 youtube dnalion7 youtube dna templates google slides dna template strand translation dna template synthesis dna template synthesis of polymers dna test for dogs dna testing center near me dna testing comparison chart dna testing cost dna testing ethics dna testing for ancestry dna testing for birds dna testing for cats dna testing for dogs dna testing for health dna testing for paternity dna testing fraud dna testing free online dna testing heritage dna testing kits dna testing kits/fl dna testing kits 2020 dna testing kits for paternity dna testing kits for paternity hair dna testing kits guides dna testing lab dna testing sites dna testing song dna testing while pregnant dna tests equipment shunned by fly fishers crossword
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