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Sigma-Aldrich

Nova Taq Hot Start DNA Polymerase

Heat-activatable modified form of recombinant Taq DNA polymerase

Synonim(y):

Hot-start Taq DNA polymerase, NovaTaq HS DNA polymerase, hot start PCR

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About This Item

Kod UNSPSC:
41106314
NACRES:
NA.54

pochodzenie biologiczne

bacterial (Thermus aquaticus)

Poziom jakości

rekombinowane

expressed in E. coli

Postać

liquid

zastosowanie

sufficient for 1000 reactions
sufficient for 200 reactions

Właściwości

dNTPs included: no
hotstart

producent / nazwa handlowa

Novagen®

warunki przechowywania

OK to freeze

metody

PCR: suitable

moc wejściowa

purified DNA

przydatność

suitable for PCR

Warunki transportu

wet ice

temp. przechowywania

−20°C

Opis ogólny

NovaTaq Hot Start DNA Polymerase is a chemically modified Taq DNA Polymerase, which is inactive at room temperature. This polymerase is a derived recombinant form of Thermus aquaticus DNA polymerase. The enzyme exhibits a 5′→3′ DNA polymerase activity and lacks 3′→5′ exonuclease activity. The enzyme provides improved specificity when compared to standard Taq polymerase and can eliminate the presence of nonspecific amplification such as primer-dimers and mis-primed products. The enzyme must be activated by heat treatment (7–10 min at 95°C), after which thermal cycling can proceed. NovaTaq Hot Start DNA Polymerase generates PCR products with 3′-dA overhangs, suitable for cloning with Novagen® Perfectly Blunt®, Acceptor, and LIC Vector Kits. NovaTaq Hot Start DNA Polymerase is a component of NovaTaq Hot Start Master Mix Kit.

Source: Recombinant Thermus aquaticus DNA polymerase expressed in E. coli
Concentration: 5.0 U/μl
Endonuclease:None detected
Exonuclease: None detected
Amplification efficiency: Functional PCR
Storage: –20°

Zastosowanie

NovaTaq Hot Start DNA Polymerase has been used in polymerase chain reaction (PCR) amplification. It is suitable for use in Hot Start routine PCR.

Cechy i korzyści

  • Higher PCR specificity and yield
  • Improved low-copy target amplification
  • Ambient temperature setup compatible with automation
  • Target amplification of up to 5 kbp
  • Ideal for quantitative and high-throughput PCR applications

Komponenty

•250 U or 5 × 250 UNovaTaq Hot Start DNA Polymerase (5 U/µl)

•1.5 ml or 5 × 1.5 ml10X NovaTaq Hot Start Buffer•1.5 ml or 5 × 1.5 ml25 mM MgCl₂

Ostrzeżenie

Toxicity: Multiple Toxicity Values, refer to MSDS (O)

Definicja jednostki

One unit is defined as the amount of enzyme that will catalyze the incorporation of 10 nmol of dNTP into acid-insoluble form in 30 min at 72°C, in a reaction containing 25 mM TAPS (tris-[hydroxymethyl]-methyl-amino-propane-sulfonic acid, sodium salt), pH 9.3 at 25°C, 50 mM KCl, 2 mM MgCl₂, 1 mM 2-mercaptoethanol, 0.2 mM dATP, dGTP, and dTTP, 0.1 µM [α-³²P]dCTP, and 12.5 µg activated salmon sperm DNA in a volume of 50 µl.

Informacje prawne

Purchase of this product includes an immunity from suit under patents specified in the product insert to use only the amount purchased for the purchaser′s own internal research. No other patents rights are conveyed expressly, by implication, or by estoppel. Further information on purchasing licenses may be obtained by contacting the Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California, 94404, USA.
NOVAGEN is a registered trademark of Merck KGaA, Darmstadt, Germany
Perfectly Blunt is a registered trademark of Merck KGaA, Darmstadt, Germany
This page may contain text that has been machine translated.

Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

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Odwiedź Bibliotekę dokumentów

Factors affecting quantitative PCR assay of Plesiomonas shigelloides.
Gu W and Levin R E
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Environmental health perspectives, 118(11), 1597-1602 (2010-06-22)
Evidence of potent rodent carcinogenicity via an unclear mechanism suggests that furan in various foods [leading to an intake of up to 3.5 microg/kg body weight (bw)/day] may present a potential risk to human health. We tested the hypothesis that

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