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TAQ-RO

Roche

Taq DNA Polymerase, 5 U/μl

optimum pH ~9.0 (20 °C), optimum reaction temp. 72 °C

Synonim(y):

dna amplification, pcr, polymerase, pcr, primer extension, dna amplification, primer extension

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About This Item

Numer EC enzymu:
Kod UNSPSC:
41106300

pochodzenie biologiczne

bacterial (Thermus aquaticus)

Poziom jakości

rekombinowane

expressed in E. coli

klasa czystości

Molecular Biology

Postać

liquid

zastosowanie

sufficient for ≤1,000 reactions (11146173001)
sufficient for ≤10,000 reactions (11435094001)
sufficient for ≤2,000 reactions (11418432001)
sufficient for ≤5,000 reactions (11596594001)
sufficient for ≤200 reactions (11146165001)

aktywność właściwa

5 U/μL

masa cząsteczkowa

95 kDa

opakowanie

pkg of 1,000 U (11418432001 [4 x 250 U])
pkg of 2,500 U (11596594001 [10 x 250 U])
pkg of 5,000 U (11435094001 [20 x 250 U])
pkg of 100 U (11146165001)
pkg of 500 U (11146173001 [1 x 500 U])

producent / nazwa handlowa

Roche

Parametry

72 °C optimum reaction temp.

metody

DNA sequencing: suitable
PCR: suitable

kolor

colorless

optymalne pH

~9.0 (20 °C)

rozpuszczalność

water: miscible

przydatność

suitable for molecular biology

numer dostępu NCBI

numer dostępu UniProt

Zastosowanie

genomic analysis
life science and biopharma

obecność zanieczyszczeń

Nicking activity 30 units, none detected
Ribonuclease 30 units, none detected
Unspecific endonucleases 30 units, none detected

temp. przechowywania

−20°C

Opis ogólny

Taq DNA Polymerase is a highly processive 5′→3′ DNA polymerase that lacks 3′→5′ exonuclease activity. It is a single polypeptide chain with a molecular weight of approximately 95 kDa.
Taq DNA Polymerase was originally isolated from the thermophilic eubacterium Thermus aquaticus BM, a strain lacking Taq I restriction endonuclease. The enzyme was cloned in E.coli.

Zastosowanie

Taq DNA Polymerase can be used in simple, routine PCR. Roche Applied Science Taq DNA polymerase is held to rigorous purity and quality standards. This preparation of recombinant Taq DNA Polymerase can be applied for:
  • PCR
  • RT-PCR
  • qPCR
  • Other primer-extension reactions, such as sequencing and labeling

Cechy i korzyści

Reliable reproducible results:
High lot-to-lot consistency.
No need to test each lot:
Taq DNA Polymerase is rigorously tested.
Prevent PCR carryover:
dUTP incorporation combination with Uracil-DNA Glycosylase prevents PCR cross-contamination.

Opakowanie

1 kit containing 2 components

Jakość

Routine assays have medium size amplicons and 50% GC content. Taq DNA Polymerase has no proofreading or hot start features. It is optimally active at +75°C and pH 9.
Lack of restriction endonuclease:
The enzyme originally isolated from T. aquaticus BM lacks Taq I restriction endonuclease activity.Each lot is PCR tested using λDNA. Each lot is also tested for the absence of exo- and endonucleases, and nicking activities according to the current Quality Control procedures.

Definicja jednostki

One unit Taq DNA Polymerase is defined as the amount of enzyme that incorporates 10 nmol of total deoxyribonucleosidetriphosphates into acid precipitable DNA within 60 min at +65 °C under the assay conditions given above.

Unit Assay: Incubation buffer:
67 mM Tris/HCl; pH 8.3/25 °C, 5 mM MgCl2, 10 mM Mercaptoethanol, 0.2% Polydocanol, 0.2 mg/ml Gelatine, 0.2 mM each dATP, dGTP, dTTP and 0.1 mM dCTP.

Incubation procedure:
M13mp9ss, M13 primer (17mer) and 1 μCi (α-32P) dCTP are incubated with suitable dilutions of Taq DNA Polymerase in 50 μl incubation buffer at +65 °C for 60 minutes. The amount of incorporated dNTPs is determined by trichloroacetic acid precipitation.

Volume Activity: 5 U/μl

Inne uwagi

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

Informacje prawne

Use of this product is covered by US patent claims and corresponding patent claims outside the US. The purchase of this product includes a limited, non-transferable immunity from suit under the foregoing patent claims for using only this amount of product for the purchaser′s own internal research. No right under any other patent claim, no right to perform any patented method, and no right to perform commercial services of any kind, including without limitation reporting the results of purchaser′s activities for a fee or other commercial consideration, is conveyed expressly, by implication, or by estoppel. This product is for research use only. Diagnostic uses under Roche patent claims require a separate license from Roche. 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.
This page may contain text that has been machine translated.

Tylko elementy zestawu

Numer produktu
Opis

  • Taq DNA Polymerase 5 U/μl

  • PCR Buffer with MgCl<sub>2</sub> 10x concentrated

  • MgCl<sub>2</sub> Stock Solution

  • PCR Buffer without MgCl<sub>2</sub>

Zwroty wskazujące rodzaj zagrożenia

Zwroty wskazujące środki ostrożności

Klasyfikacja zagrożeń

Aquatic Chronic 3

Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

does not flash

Temperatura zapłonu (°C)

does not flash


Certyfikaty analizy (CoA)

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

H N Chinivasagam et al.
Journal of applied microbiology, 103(2), 418-426 (2007-07-26)
To investigate the occurrence and levels of Arcobacter spp. in pig effluent ponds and effluent-treated soil. A Most Probable Number (MPN) method was developed to assess the levels of Arcobacter spp. in seven pig effluent ponds and six effluent-treated soils
Pattabhiraman Shankaranarayanan et al.
Nature protocols, 7(2), 328-338 (2012-01-28)
Linear amplification of DNA (LinDA) by T7 polymerase is a versatile and robust method for generating sufficient amounts of DNA for genome-wide studies with minute amounts of cells. LinDA can be coupled to a great number of global profiling technologies.
Mónica Alejandra Rosales-Reynoso et al.
Archives of medical research, 41(2), 110-118 (2010-05-18)
Although sporadic cases of cancer in patients with fragile X syndrome (FXS) have been reported, extensive studies carried out in Denmark and Finland concluded that cancer incidence in these patients is lower than in the general population. On the other

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