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OneTaq® Hot Start 2X Master Mix with Standard Buffer
OneTaq® DNA Polymerase is an optimized blend of Taq and Deep Vent® DNA polymerases for use with routine and difficult PCR experiments.
Obtain high yields across a wide range of AT / GC content
2X higher fidelity than Taq
Hot Start feature enables room temperature reaction setup
Master mix is a 2X concentrated solution containing everything needed for robust amplification
精选视频
How to Amplify GC-rich DNA
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产品信息
OneTaq® Hot Start 2X Master Mix with Standard Buffer is an optimized blend of Taq and Deep Vent® DNA Polymerases combined with an aptamer-based inhibitor. This enzyme blend is ideally suited to routine PCR applications from a variety of templates, including pure DNA solutions, bacterial colonies and cDNA products. The 3´→5´ exonuclease activity of Deep Vent DNA Polymerase increases the fidelity and robust amplification of Taq DNA Polymerase (1). The hot start nature of the enzyme offers convenience with decreased interference from primer dimers and secondary products. The convenient master mix formulation contains dNTPs, MgCl2 and other buffer components and stabilizers listed below, requiring only the addition of primers and DNA template for robust amplification
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,
Master Mixes Products
应用:
Hot Start PCR,
Fast PCR,
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
M0484S
-20
OneTaq® Hot Start 2X Master Mix with Standard Buffer
M0484SVIAL
-20
2 x 1.25 ml
2 X
M0484L
-20
OneTaq® Hot Start 2X Master Mix with Standard Buffer
M0484SVIAL
-20
10 x 1.25 ml
2 X
特性和用法
1X 预混液组分
20 mM Tris-HCl 22 mM KCl 22 mM NH4Cl 1.8 mM MgCl2 5% Glycerol 0.06% IGEPAL® CA-630 0.05% Tween® 20 0.2 mM dNTPs 25 units/ml OneTaq Hot Start DNA Polymerase pH 8.9 @ 25°C
热失活
否
单位活性检测条件
1X ThermoPol® Reaction Buffer, 200 μM dNTPs including [3H]-dTTP and 15 nM primed M13 DNA.
优势和特性
应用特性
High Throughput PCR
High Sensitivity PCR
Routine PCR
AT-rich PCR
Colony PCR
Long PCR (up to ~6 kb genomic)
相关产品
相关产品
Magnesium Chloride (MgCl2) Solution
OneTaq® DNA Polymerase
OneTaq® Hot Start 2X Master Mix with GC Buffer
OneTaq® Hot Start DNA Polymerase
OneTaq® Quick-Load® 2X Master Mix with Standard Buffer
OneTaq® Hot Start Quick-Load® 2X Master Mix with GC Buffer
OneTaq® 2X Master Mix with Standard Buffer
注意事项
Product specifications for individual components in the OneTaq Hot Start 2X Master Mix with Standard Buffer are available separately.
OneTaq Hot Start 2X Master Mix with Standard Buffer is stable for fifteen freeze-thaw cycles when stored at -20°C.
OneTaq Hot Start 2X Master Mix with Standard Buffer is also stable for one month at 4°C, so for frequent use, an aliquot may be kept at 4°C.
Saiki, R.K. et al. (1994). Science. 91, 2216-2220.
Powell, L.M. et al. (1987). Cell. 50, 831-840.
Sun, Y, Hegamyer, G. and Colburn, N. (1993). Biotechniques. 15, 372-374.
操作说明、说明书 & 用法
操作说明
Protocol for OneTaq Hot Start 2X Master Mix with Standard Buffer (M0484)
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
How is OneTaq DNA Polymerase different from LongAmp™ Taq DNA Polymerase?
What are the stability and storage requirements of the OneTaq® Master Mixes?
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?
What type of DNA ends result from a primer extension reaction or a PCR using OneTaq® DNA Polymerase?
How should I set up a PCR using the OneTaq® Hot Start Master Mixes?
Can I use my regular Taq-based cycling conditions for OneTaq® Hot Start DNA Polymerase based products?
How do I activate OneTaq® Hot Start Polymerase?
问题解决指南
PCR Troubleshooting Guide
实验技巧
Try using a master mix with OneTaq Hot Start DNA Polymerase to achieve highly specific and sensitive PCR amplification.
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
Gorski L, Walker S, Liang AS, Nguyen KM, Govoni J, et al. (2014) Comparison of Subtypes of Listeria monocytogenes Isolates from Naturally Contaminated Watershed Samples with and without a Selective Secondary Enrichment PLoS One; 9(3), e92467. PubMedID: 24651315, DOI: 10.1371/journal.pone.0092467
专题文章
Using aptamers to control enzyme activities: Hot Start Taq and beyond