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Merck

TAQN-RO

Roche

Taq DNA Polymerase, dNTPack

suitable for PCR, optimum pH ~9.0 (20 °C), dNTPs included

Szinonimák:

dna amplification, pcr, polymerase, primer extension

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

Enzyme Commission szám:
UNSPSC kód:
41106300
NACRES:
NA.55

biológiai forrás

bacterial (Thermus aquaticus BM)

Minőségi szint

rekombináns

expressed in E. coli

leírás

5 U/βl
Number of Reactions:
If 1.25 U are used per 50 μL reaction, Taq DNA Polymerase, dNTPack is designed for approximately sufficient for number of reactions, mentioned in the usage.

form

liquid

használat

sufficient for 2,000 reactions (04728904001)
sufficient for 4,000 reactions (04728858001)
sufficient for 400 reactions (04728874001)
sufficient for 80 reactions (04728866001)
sufficient for 800 reactions (04728882001)

molekulatömeg

95  kDa

Jellemzők

dNTPs included
hotstart: no

kiszerelés

pkg of 1,000 U (04728882001 [4 x 250 U])
pkg of 2,500 U (04728904001 [10 x 250 U])
pkg of 5,000 U (04728858001 [20 x 250 U])
pkg of 100 U (04728866001)
pkg of 500 U (04728874001 [2 x 250 U])

gyártó/kereskedő neve

Roche

koncentráció

0.025 units/reaction

parameter

72 °C optimum reaction temp.

technika/technikák

PCR: suitable

szín

colorless

bemenet

purified DNA

optimális pH

~9.0 (20 °C)

oldhatóság

water: soluble

alkalmasság

suitable for PCR and automated sequencing reactions

UniProt elérési szám

alkalmazás(ok)

genomic analysis
life science and biopharma

idegen aktivitás

endonucleases, none detected
exonuclease, none detected
nicking activitities, none detected

tárolási hőmérséklet

−20°C

Általános leírás

Contents
Taq DNA Polymerase, 5 U/μl
PCR Buffer, 10x concentrated, with MgCl2
PCR Nucleotide Mix

For maximum convenience, select the ready-to-use 2x concentrated PCR Master.
Each dNTPack contains 10 mM additive-free sodium salt nucleotides as a ready-to-use mix.
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 preparation obtained from E.coli is free of nonspecific engo- or exonucleases according to the current quality control procedures.

Alkalmazás

Achieve the most consistent results in simple, routine PCR by using Roche Applied Science Taq DNA Polymerase, which is held to our rigorous purity and quality standards. The Taq DNA Polymerase, dNTPack, combines our standard preparation (5 U/μl) of recombinant Taq DNA Polymerase with our convenient, ready-to-use PCR Nucleotide Mix. In all other respects, this preparation is identical to our standard preparation and can be used for:

  • PCR
  • RT-PCR
  • Other primer-extension reactions, such as sequencing and labeling

Tulajdonságok és előnyök

  • 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.

Kiszerelés

1 kit containing 3 components

Minőség

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.

Egység definíció

One unit Taq DNA Polymerase is defined as the amount of enzyme that incorporates 10 nmol of total deoxyribonucleosidetriphosphates into acid precipitable DNA within 30 minutes at +75 °C under the assay conditions stated under unit assay.

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

Tárolás és stabilitás

Containers which are opened must be carefully resealed and
kept upright to prevent leakage

Egyéb megjegyzések

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

Jogi információk

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.

Kit Components Only

Product No.
Leírás

  • Taq DNA Polymerase 5 U/μl

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

  • PCR Nucleotide Mix

Figyelmeztető mondatok

Óvintézkedésre vonatkozó mondatok

Veszélyességi osztályok

Aquatic Chronic 3

Tárolási osztály kódja

12 - Non Combustible Liquids

WGK

WGK 2

Lobbanási pont (F)

does not flash

Lobbanási pont (C)

does not flash


Analitikai tanúsítványok (COA)

Analitikai tanúsítványok (COA) keresése a termék sarzs-/tételszámának megadásával. A sarzs- és tételszámok a termék címkéjén találhatók, a „Lot” vagy „Batch” szavak után.

Már rendelkezik ezzel a termékkel?

Az Ön által nemrégiben megvásárolt termékekre vonatkozó dokumentumokat a Dokumentumtárban találja.

Dokumentumtár megtekintése

Harri Sihto et al.
Journal of the National Cancer Institute, 101(13), 938-945 (2009-06-19)
Merkel cell carcinoma is a rare malignancy of the skin. Integration of Merkel cell polyomavirus (MCPyV) DNA to the tumor genome is frequent in these cancers. The clinical consequences of MCPyV infection are unknown. We analyzed formalin-fixed paraffin-embedded Merkel cell
Tensin2 Is a Novel Diagnostic Marker in GIST, Associated with Gastric Location and Non-Metastatic Tumors
Salmikangas, et al.
Cancers, 14 (2022)
Development of Microsatellites for the Philippine Eagle, Pithecophaga jefferyi, Using Next-generation Sequencing.
Ong PS, et al.
Journal of Separation Science (2019)
Gemma Moir-Meyer et al.
Methods and protocols, 1(3) (2019-06-06)
The study of cellular processes and gene regulation in terminal erythroid development has been greatly facilitated by the generation of an immortalised erythroid cell line derived from Human Umbilical Derived Erythroid Precursors, termed HUDEP-2 cells. The ability to efficiently genome
Xiuhui Shi et al.
Gastroenterology, 162(7), 2004-2017 (2022-02-18)
Pancreatic cancer has the highest prevalence of cancer-associated cachexia among all cancers. ZIP4 promotes pancreatic cancer progression by regulating oncogenic miR-373, and perturbation of circular RNAs (circRNAs) is associated with cancer aggressiveness. This study aimed to identify circRNAs involved in ZIP4/miR-373-driven

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