上海金畔生物科技有限公司代理New England Biolabs(NEB)酶试剂全线产品,欢迎访问官网了解更多产品信息和订购。
OneTaq® 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
Master mix is a 2X concentrated solution containing everything needed for robust amplification
精选视频
How to Amplify GC-rich DNA
观看其他视频
产品信息
OneTaq® 2X Master Mix with Standard Buffer is an optimized blend of Taq and Deep Vent® DNA Polymerases 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 convenient master mix formulation contains dNTPs, MgCl2, buffer components and stabilizers, 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:
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
M0482S
-20
OneTaq® 2X Master Mix with Standard Buffer
M0482SVIAL
-20
2 x 1.25 ml
2 X
M0482L
-20
OneTaq® 2X Master Mix with Standard Buffer
M0482SVIAL
-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 0.05% Tween® 20 0.06% IGEPAL® CA-630 0.2 mM dNTPs 25 units/ml OneTaq® 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
GC-rich PCR
High Sensitivity PCR
High Throughput PCR
Colony PCR
Long PCR (up to ~6 kb genomic)
AT-rich PCR
相关产品
相关产品
Magnesium Chloride (MgCl2) Solution
OneTaq® DNA Polymerase
OneTaq® Hot Start DNA Polymerase
OneTaq® Quick-Load® 2X Master Mix with Standard Buffer
OneTaq® Hot Start 2X Master Mix with Standard Buffer
注意事项
OneTaq 2X Master Mix with Standard Buffer is stable for fifteen freeze-thaw cycles when stored at -20°C.
OneTaq 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.
Product specifications for individual components in the OneTaq 2X Master Mix with Standard Buffer 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.
Sun,y., Hegamyer, G. and Colburn,N. (1993). Biotechniques. 15, 372-374.
Sarker, G., Kapelner, S. and Summer, S.S. (1990). Nuclear Acids Res.. 18, 7465.
Magda Matoušková, Pavel Veselý, Petr Daniel, Giada Mattiuzzo, Ralph Hector, Linda Scobie, Yasuhiro Takeuchi and Jiří Hejnar (2013). The Role of DNA Methylation in Expression and Transmission of Procine Endogenous Retrovirus. Journal of Virology. JVI.03262-12,
操作说明、说明书 & 用法
操作说明
Protocol for OneTaq® 2X Master Mix with Standard Buffer (M0482)
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 should I set up a PCR using the OneTaq® Master Mixes?
Can I use my regular Taq-based cycling conditions for OneTaq® DNA Polymerase based products?
Can I use OneTaq® DNA Polymerase in “hot start” PCR to help with specificity or primer dimer problems?
What are the stability and storage requirements of the OneTaq® Master Mixes?
Can OneTaq® DNA Polymerase be used in colony PCR?
What type of DNA ends result from a primer extension reaction or a PCR using OneTaq® DNA Polymerase?
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?
How is OneTaq DNA Polymerase different from LongAmp™ Taq DNA Polymerase?
问题解决指南
PCR Troubleshooting Guide
实验技巧
Use OneTaq 2X Master Mix with Standard Buffer to amplify routine targets with up to 65% GC content.
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
Stöhr AC, López-Bueno A, Blahak S, Caeiro MF, Rosa GM, Alves de Matos AP, Martel A, Alejo A, Marschang RE (2015) Phylogeny and differentiation of reptilian and amphibian ranaviruses detected in europe PLoS One; 10(2), e0118633. PubMedID: 25706285, DOI: 10.1371/journal.pone.0118633
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Bulk packaging may also be available and requested for large recurring orders. Learn More
产品信息
LunaScript RT SuperMix is an optimized master mix for first strand cDNA synthesis and can be used in amplicon sequencing or a two-step RT-qPCR workflow. It features the thermostable Luna Reverse Transcriptase, which supports cDNA synthesis at elevated temperatures. Murine RNase Inhibitor is also included to protect template RNA from degradation. LunaScript RT SuperMix contains random hexamer and poly-dT primers, allowing even coverage across the length of the RNA targets. In addition, LunaScript RT SuperMix contains a blue dye, providing a visual indicator that can be followed throughout the two-step RT-qPCR process. The product offers robust, linear, and sensitive detection using total RNA inputs as high as 1 µg and as low as single copies of RNA.
For RT-PCR, RNA-seq, and other applications, LunaScript RT Master Mix Kit (Primer-free) (NEB #E3025) is an optimized master mix containing all the necessary components for first strand cDNA synthesis, except for primers. The mix is compatible with random primers, oligo dT primers, and gene-specific primers, enabling maximum cDNA synthesis flexibility. Learn more here.
In comparison to the LunaScript kit version (NEB #E3010), this LunaScript product does not contain a No-RT Control Mix or nuclease-free water. More details can be found below:
产品类别:
Luna® qPCR & RT-qPCR Products
应用:
qPCR & RT-qPCR,
Reverse Transcription (cDNA Synthesis)
试剂盒组成
试剂盒组成
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
E3010S
-20
LunaScript® RT SuperMix
M3010SVIAL
-20
1 x 0.1 ml
5 X
No-RT Control Mix
M3011SVIAL
-20
1 x 0.1 ml
5 X
Nuclease-free Water
B1502AVIAL
-20
1 x 1.5 ml
不适用
E3010L
-20
LunaScript® RT SuperMix
M3010LVIAL
-20
1 x 0.4 ml
5 X
No-RT Control Mix
M3011LVIAL
-20
1 x 0.4 ml
5 X
Nuclease-free Water
B1502AVIAL
-20
4 x 1.5 ml
不适用
特性和用法
相关产品
相关产品
Luna® Universal qPCR Master Mix
Luna® Universal Probe qPCR Master Mix
Antarctic Thermolabile UDG
Monarch® Total RNA Miniprep Kit
操作说明、说明书 & 用法
操作说明
Protocol for LunaScript® RT SuperMix Kit (E3010)
Protocol for Two-step RT-qPCR using the LunaScript® RT SuperMix Kit (NEB #E3010) and the Luna® Universal qPCR Master Mix (NEB #M3003) or Luna Universal Probe qPCR Master Mix (NEB #M3004)
说明书
产品说明书包含产品使用的详细信息、产品配方和质控分析。
manualE3010
应用实例
Facilitating Detection of SARS-CoV-2 Directly from Patient Samples: Precursor Studies with RT-qPCR and Colorimetric RT-LAMP Reagents
FAQs & 问题解决指南
FAQs
Can I use RNA samples purified from different storage conditions such as RNALater in my LunaScript® cDNA synthesis reactions?
Can I add gene-specific primers in my LunaScript® cDNA synthesis reaction?
Can I set up my cDNA synthesis reaction at room temperature when using the LunaScript® RT SuperMix?
Can I use a shorter incubation time for my cDNA synthesis reaction when using the LunaScript® RT SuperMix?
Can I use LunaScript® cDNA products directly in qPCR? How much can I use for detection in a qPCR reaction?
How much RNA template should I use in my LunaScript® cDNA synthesis reactions?
How should I store LunaScript® cDNA products?
How should I choose between a one-step RT-qPCR or two-step RT-qPCR approach?
Should I include a No-Reverse Transcriptase (RT) control reaction when setting up my cDNA synthesis reaction?
What qPCR reagents do you recommend for detection of cDNA products?
What temperature should I use for my LunaScript® cDNA synthesis reaction?
Why do I have low cDNA yields?
Will the blue dye in the LunaScript® RT SuperMix interfere with detection?
How do I choose between the first strand cDNA synthesis kits from NEB?
When using LunaScript cDNA products in downstream PCR (i.e., two-step RT-PCR), what volumes and PCR products can be used?
Can I use LunaScript RT SuperMix in RNA-seq workflows?
How do I choose between LunaScript® RT SuperMix Kit and ProtoScript first strand cDNA synthesis kits?
Can I use a shorter incubation time for my cDNA synthesis reaction when using the LunaScript® RT Master Mix (Primer-free)? Does longer incubation increase the yield of cDNA?
上海金畔生物科技有限公司代理New England Biolabs(NEB)酶试剂全线产品,欢迎访问官网了解更多产品信息和订购。
NEBuffer™ 1.1
This product will be discontinued on 12/15/2021 and replaced with NEBuffer™ Set (r1.1, r2.1, r3.1 and rCutSmart™.
Catalog # B7201 was discontinued on December 15, 2021
New England Biolabs provides a color-coded 10X NEBuffer with each restriction endonuclease to ensure optimal (100%) activity. Most of our enzymes are supplied with one of four standard NEBuffers. Visit NEBCutSmart.com for details.
产品信息
New England Biolabs provides a colorcoded 10X NEBuffer with each restriction endonuclease to ensure optimal (100%) activity. Most of our enzymes are supplied with one of four standard NEBuffers. Occasionally, an enzyme has specific buffer requirements not met by one of the four standard NEBuffers, in which case the enzyme is supplied with its own unique NEBuffer.
产品类别:
Discontinued Products
特性和用法
1X 缓冲液组分
10 mM Bis-Tris-Propane-HCl 10 mM MgCl2 100 µg/ml BSA pH [email protected]°C
相关产品
相关产品
Monarch® Plasmid Miniprep Kit
Monarch® DNA Gel Extraction Kit
Monarch® PCR & DNA Cleanup Kit (5 μg)
注意事项
The pH of 10X NEBuffer 1.1 is between pH 6.9 and 7.1.
工具 & 资源
选择指南
NEB Diluent and Buffer Table
FAQs & 问题解决指南
FAQs
What is supplied with the NEBuffer 1.1 pack?
How should the NEBuffer be used?
The buffer arrived thawed. Are the buffer and the enzyme still active?
You have replaced NEBuffer 1 with NEbuffer 1.1, NEBuffer 2 with NEBuffer 2.1, and NEBuffer 3 with 3.1. Where is NEBuffer 4.1?
Why did you add BSA into all the restriction enzyme reaction buffers?
Why did you remove DTT from your restriction enzyme buffers?
I don’t want to use BSA in my buffer. What are my options?
Why is my Restriction Enzyme not cutting DNA?
Why do I see additional DNA bands on my gel after a restriction digest?
Why do I see a DNA smear on an agarose gel after a restriction digest?
How many nucleotides do I have to add adjacent to the RE recognition site in order to get efficient cutting?
Are the alkaline phosphatases active in NEBuffers?
上海金畔生物科技有限公司代理New England Biolabs(NEB)酶试剂全线产品,欢迎访问官网了解更多产品信息和订购。
NEBuffer™ 1.1
This product will be discontinued on 12/15/2021 and replaced with NEBuffer™ Set (r1.1, r2.1, r3.1 and rCutSmart™.
Catalog # B7201 was discontinued on December 15, 2021
New England Biolabs provides a color-coded 10X NEBuffer with each restriction endonuclease to ensure optimal (100%) activity. Most of our enzymes are supplied with one of four standard NEBuffers. Visit NEBCutSmart.com for details.
产品信息
New England Biolabs provides a colorcoded 10X NEBuffer with each restriction endonuclease to ensure optimal (100%) activity. Most of our enzymes are supplied with one of four standard NEBuffers. Occasionally, an enzyme has specific buffer requirements not met by one of the four standard NEBuffers, in which case the enzyme is supplied with its own unique NEBuffer.
产品类别:
Discontinued Products
特性和用法
1X 缓冲液组分
10 mM Bis-Tris-Propane-HCl 10 mM MgCl2 100 µg/ml BSA pH [email protected]°C
相关产品
相关产品
Monarch® Plasmid Miniprep Kit
Monarch® DNA Gel Extraction Kit
Monarch® PCR & DNA Cleanup Kit (5 μg)
注意事项
The pH of 10X NEBuffer 1.1 is between pH 6.9 and 7.1.
工具 & 资源
选择指南
NEB Diluent and Buffer Table
FAQs & 问题解决指南
FAQs
What is supplied with the NEBuffer 1.1 pack?
How should the NEBuffer be used?
The buffer arrived thawed. Are the buffer and the enzyme still active?
You have replaced NEBuffer 1 with NEbuffer 1.1, NEBuffer 2 with NEBuffer 2.1, and NEBuffer 3 with 3.1. Where is NEBuffer 4.1?
Why did you add BSA into all the restriction enzyme reaction buffers?
Why did you remove DTT from your restriction enzyme buffers?
I don’t want to use BSA in my buffer. What are my options?
Why is my Restriction Enzyme not cutting DNA?
Why do I see additional DNA bands on my gel after a restriction digest?
Why do I see a DNA smear on an agarose gel after a restriction digest?
How many nucleotides do I have to add adjacent to the RE recognition site in order to get efficient cutting?
Are the alkaline phosphatases active in NEBuffers?
上海金畔生物科技有限公司代理New England Biolabs(NEB)酶试剂全线产品,欢迎访问官网了解更多产品信息和订购。
NEBuffer™ 2.1
This product was discontinued on 12/15/2021 and replaced with NEBuffer r2.1.
Catalog # B7202 was discontinued on December 15, 2021
New England Biolabs provides a color-coded 10X NEBuffer with each restriction endonuclease to ensure optimal (100%) activity.
Most of our enzymes are supplied with one of four standard NEBuffers. Visit NEBCutSmart.com for details.
产品信息
New England Biolabs provides a colorcoded 10X NEBuffer with each restriction endonuclease to ensure optimal (100%) activity. Most of our enzymes are supplied with one of four standard NEBuffers. Occasionally, an enzyme has specific buffer requirements not met by one of the four standard NEBuffers, in which case the enzyme is supplied with its own unique NEBuffer.
产品类别:
Discontinued Products
特性和用法
1X 缓冲液组分
50 mM NaCl 10 mM Tris-HCl 10 mM MgCl2 100 µg/ml BSA pH [email protected]°C
相关产品
相关产品
Monarch® Plasmid Miniprep Kit
Monarch® DNA Gel Extraction Kit
Monarch® PCR & DNA Cleanup Kit (5 μg)
注意事项
The pH of 10X NEBuffer 2.1 is between pH 7.8 and 8.0.
工具 & 资源
选择指南
NEB Diluent and Buffer Table
FAQs & 问题解决指南
FAQs
What is supplied with the NEBuffer 2.1 pack?
How should the NEBuffer be used?
The buffer arrived thawed. Are the buffer and the enzyme still active?
You have replaced NEBuffer 1 with NEbuffer 1.1, NEBuffer 2 with NEBuffer 2.1, and NEBuffer 3 with 3.1. Where is NEBuffer 4.1?
Why did you add BSA into all the restriction enzyme reaction buffers?
Why did you remove DTT from your restriction enzyme buffers?
I don’t want to use BSA in my buffer. What are my options?
Why is my Restriction Enzyme not cutting DNA?
Why do I see additional DNA bands on my gel after a restriction digest?
Why do I see a DNA smear on an agarose gel after a restriction digest?
How many nucleotides do I have to add adjacent to the RE recognition site in order to get efficient cutting?
Are the alkaline phosphatases active in NEBuffers?