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OneTaq® DNA Polymerase
The ONE polymerase for your endpoint PCR needs. OneTaq DNA Polymerase is an optimized blend of Taq and Deep Vent® DNA polymerases for use with routine and difficult PCR experiments.
2X higher fidelity than Taq
Ideal for routine, AT- or GC-rich templates
Hot start and master mix versions available
精选视频
How to Amplify GC-rich DNA
观看其他视频
产品信息
The 3´→ 5´ exonuclease activity of Deep Vent DNA Polymerase increases the fidelity and robust amplification of Taq DNA Polymerase (1) . The OneTaq Reaction Buffers and High GC Enhancer have been formulated for robust yields with minimal optimization, regardless of a template’s GC content.
OneTaq DNA Polymerase is supplied with two 5X buffers: (Standard and GC), as well as a High GC Enhancer solution. For most routine and/or AT-rich amplicons (Lambda, etc.) or complex amplicons with up to ~65% GC content, OneTaq Standard Reaction Buffer provides robust amplification. For GC-rich amplicons, the OneTaq GC Reaction Buffer can improve both performance and yield. For particularly high GC or difficult amplicons, the OneTaq High GC Enhancer can be added at a final concentration of 10–20% to reactions containing OneTaq GC Reaction Buffer.
产品来源
An E. coli strain that carries the Taq DNA Polymerase gene from Thermus aquaticus YT-1 and an E. coli strain that carries the Deep Vent® DNA Polymerase gene from Pyrococcus species GB-D.
产品类别:
OneTaq® DNA Polymerases Products,
Taq DNA Polymerase Products
应用:
Multiplex PCR,
Specialty PCR,
Routine PCR,
PCR
产品组分信息
产品组分信息
本产品提供以下试剂或组分:
NEB #
名称
组分货号
储存温度
数量
浓度
M0480S
-20
OneTaq® DNA Polymerase
M0480SVIAL
-20
1 x 0.04 ml
5,000 units/ml
OneTaq® Standard Reaction Buffer Pack
B9022SVIAL
-20
1 x 2 ml
5 X
OneTaq® GC Reaction Buffer Pack
B9023SVIAL
-20
1 x 2 ml
5 X
OneTaq® High GC Enhancer
B9026AVIAL
-20
1 x 2 ml
不适用
M0480L
-20
OneTaq® DNA Polymerase
M0480LVIAL
-20
1 x 0.2 ml
5,000 units/ml
OneTaq® Standard Reaction Buffer Pack
B9022SVIAL
-20
5 x 2 ml
5 X
OneTaq® GC Reaction Buffer Pack
B9023SVIAL
-20
3 x 2 ml
5 X
OneTaq® High GC Enhancer
B9026AVIAL
-20
3 x 2 ml
不适用
M0480X
-20
OneTaq® DNA Polymerase
M0480LVIAL
-20
5 x 0.2 ml
5,000 units/ml
OneTaq® Standard Reaction Buffer Pack
B9022SVIAL
-20
25 x 2 ml
5 X
OneTaq® GC Reaction Buffer Pack
B9023SVIAL
-20
15 x 2 ml
5 X
OneTaq® High GC Enhancer
B9026AVIAL
-20
15 x 2 ml
不适用
特性和用法
单位定义
One unit is defined as the amount of enzyme that will incorporate 15 nmol of dNTP into acid insoluble material in 30 minutes at 75°C.
反应条件
1X OneTaq® Standard Reaction Buffer Pack
1X OneTaq® Standard Reaction Buffer Pack 20 mM Tris-HCl 22 mM NH4Cl 22 mM KCl 1.8 mM MgCl2 0.06% IGEPAL® CA-630 0.05% Tween® 20 (pH 8.9 @ 25°C)
使用浓度
1.25 units/50μl reaction
贮存溶液
10 mM Tris-HCl 100 mM KCl 1 mM DTT 0.1 mM EDTA 50% Glycerol 0.5% Tween® 20 0.5% IGEPAL® CA-630 pH 7.4 @ 25°C
热失活
否
5′ – 3′ 核酸外切酶
Yes
3′ – 5′ 核酸外切酶
Yes
链置换
No
单位活性检测条件
1X ThermoPol® Reaction Buffer, 200 µM dNTPs including [3H]-dTTP and 15 nM primed M13 DNA
错配率
< 140x10-6bases
优势和特性
Features
Ideal for routine, AT- and GC-rich PCR
应用特性
High Sensitivity PCR
High Throughput PCR
Routine PCR
GC-rich PCR
AT-rich PCR
Colony PCR
Long PCR (up to ~6 kb genomic)
相关产品
相关产品
Deoxynucleotide (dNTP) Solution Mix
Deoxynucleotide (dNTP) Solution Set
Magnesium Chloride (MgCl2) Solution
Magnesium Sulfate (MgSO4) Solution
OneTaq® Hot Start DNA Polymerase
注意事项
The OneTaq High GC Enhancer should not be used alone. It should be added only to reactions with the OneTaq GC Reaction Buffer and will typically improve yields when other conditions have failed.
Product specifications for individual components in the OneTaq DNA Polymerase mix are available separately.
参考文献
Barnes, W.M. (1994). Proc. Natl. Acad. Sci. USA. 91, 2216-2220.
Saiki R.K. et al. (1985). Science. 230, 1350-1354.
Powell, L.M. et al. (1987). Cell. 50, 831-840.
操作说明、说明书 & 用法
操作说明
PCR Protocol for OneTaq® DNA Polymerase (M0480)
使用指南
Activity of Restriction Enzymes in PCR Buffers
Guidelines for PCR Optimization with OneTaq® and OneTaq® Hot Start DNA Polymerases
Guidelines for PCR Optimization with Thermophilic DNA Polymerases
应用实例
Robust Colony PCR from Multiple E. coli Strains using OneTaq® Quick-Load® Master Mixes
工具 & 资源
选择指南
DNA Polymerase Selection Chart
Thermophilic DNA Polymerases
Web 工具
Tm Calculator
FAQs & 问题解决指南
FAQs
Can I use my regular Taq-based cycling conditions for OneTaq® DNA Polymerase based products?
Which buffer should I use?
When should I add the High GC Enhancer?
Can OneTaq® DNA Polymerase be used in colony PCR?
How long a product can be made by OneTaq® DNA Polymerase?
Can OneTaq® DNA Polymerase be used with uracil-containing primers or bisulfite-treated DNA?
What is the fidelity of OneTaq® DNA Polymerase?
Where can I find help troubleshooting my PCR?
How should I determine an appropriate annealing temperature for my reaction?
Which buffer should I use if I want to control the level of magnesium in the reaction?
How is OneTaq DNA Polymerase different from LongAmp™ Taq DNA Polymerase?
How should I set up an amplification reaction using OneTaq®DNA Polymerase?
What type of DNA ends result from a primer extension reaction or a PCR using OneTaq® DNA Polymerase?
问题解决指南
PCR Troubleshooting Guide
实验技巧
Did you know most OneTaq reactions amplify more efficiently and robustly when you use a 68°C extension temperature?
引用 & 技术文献
引用文献
产品引用文献查找工具
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更多引用文献
Megan S Thoemmes, Daniel J Fergus, Julie Urban, Michelle Trautwein, Robert R Dunn (2014) Ubiquity and diversity of human-associated demodex mites. PLoS One; 9, e106265. PubMedID: 25162399, DOI: 10.1371/journal.pone.0106265
Matousková, M., Vesely, P., Daniel, P., Mattiuzzo, G., Hector, R.D., Scobie, L., Takeuchi, Y. and Hejnar, J. (2013) Role of DNA methylation in expression and transmission of porcine endogenous retroviruses. PLoS One; PubMedID: 23986605
Liang, Y., Basu, D., Pattathil, S., Xu, W.L., Venetos, A., Martin, S.L., Faik, A., Hahn, M.G. and Showalter, A.M. (2013) Biochemical and physiological characterization of fut4 and fut6 mutants defective in arabinogalactan-protein fucosylation in Arabidopsis. PLoS One; PubMedID: 24127514
Malyshev, D.A., Dhami, K., Quach, H.T., Lavergne, T., Ordoukhanian, P., Torkamani, A. and Romesberg, F.E. (2012) Efficient and sequence-independent replication of DNA containing a third base pair establishes a functional six-letter genetic alphabet. Proc Natl Acad Sci U S A; 109, 4503-4508. PubMedID: 22773812