Phusion Flash 高保真 PCR 预混液
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Phusion Flash 高保真 PCR 预混液
Thermo Scientific™

Phusion Flash 高保真 PCR 预混液

Thermo Scientific Phusion Flash PCR 预混液专为节省宝贵的实验室时间而开发。当使用极短的 PCR 实验方案时,即用型 2X了解更多信息
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货号反应次数
F548L500 次反应
F548S100 次反应
货号 F548L
价格(CNY)
2,138.00
飞享价
Ends: 31-Dec-2025
3,053.00
共减 915.00 (30%)
Each
添加至购物车
反应次数:
500 次反应
请求批量或定制报价
价格(CNY)
2,138.00
飞享价
Ends: 31-Dec-2025
3,053.00
共减 915.00 (30%)
Each
添加至购物车
Thermo Scientific Phusion Flash PCR 预混液专为节省宝贵的实验室时间而开发。当使用极短的 PCR 实验方案时,即用型 2X 预混液可保持反应的保真度和得率。此外,用户只需添加模板和引物,从而最大限度地减少移液步骤。

独特的预混液成分允许对低复杂度和高复杂度 DNA 模板使用极短的循环实验方案 - 每 kb 15 秒或更少。该预混液采用 Phusion Flash II DNA 聚合酶,这是一种来源于 Phusion 热启动 II 高保真 DNA 聚合酶的经修饰的校正读码 DNA 聚合酶。

特征
•极高速度:15 s/kb 或更短的延伸时间
• 热启动修改允许“零时间重新激活”
• 准确性:具有 25X Taq 保真度的校正读码 DNA 聚合酶
• 在更短的时间内获得高产量

应用

• 快速 PCR
• 高保真 PCR
• 困难(高GC含量)模板
• 获得测序模板
• 多重 PCR
• 长片段 PCR
• 克隆
• 诱变
• 微阵列

使用 Phusion DNA 聚合酶
Phusion DNA 聚合酶的退火温度设计规则和许多普通 DNA 聚合酶(如 Taq DNA 聚合酶)不一样。为了获得最佳结果,请使用 www.thermofisher.cn/tmcalculator 上的 Tm 计算器。

仅供科研使用。不可用于诊断程序。
规格
颜色Colorless
保真度(相对于 Taq)25 X
热启动内置热启动
反应次数500 次反应
突出端平末端
聚合酶Phusion Flash II DNA 聚合酶
产品类型高保真 PCR 预混液
数量500 次反应
反应形式SuperMix 或预混液
运输条件干冰
尺寸(最终产品)20 kb 或更小
最大浓度2X
适用于(应用)Hot-start PCR, High-fidelity PCR
高 GC PCR 扩增效果
反应速度快速
Unit SizeEach
内容与储存
5 x 1 mL Phusion Flash 预混液,在 -20°C 下储存。

常见问题解答 (FAQ)

What is the difference between Phusion Flash High-Fidelity PCR Master Mix and Phusion Hot Start II High-Fidelity PCR Master Mix?

Phusion Hot Start II High-Fidelity PCR Master Mix is a 2X ready-to-use solution based on Phusion Hot Start II DNA Polymerase. It is designed for the highest fidelity (52X Taq) and specificity. Phusion Flash High-Fidelity PCR Master Mix is based on a modified Phusion Hot Start II DNA Polymerase, which allows for extremely short cycling times and features somewhat lower fidelity (25X Taq).

Do Phusion DNA Polymerases add the non-template dependent 3'-A overhang?

Phusion DNA Polymerases generate blunt end products; therefore, blunt end cloning is recommended. If TA cloning is required, it can be performed by adding A overhangs to the blunt PCR product with e.g. Taq DNA Polymerase (Cat. No. EP0401). However, before adding the overhangs it is very important to remove all the Phusion DNA Polymerase by purifying the PCR product carefully, as the proofreading activity in Phusion DNA Polymerase is very strong. Any remaining Phusion DNA Polymerase will degrade the A overhangs, thus creating blunt ends again.

Can Phusion DNA Polymerases extend at 1 second/kb?

Yes it is possible, especially when amplifying smaller amplicons. Processivity of Phusion DNA Polymerases is 10 times that of Pfu. We recommend extension times of 15 s/kb for Phusion Flash PCR Master Mix. 15 s/kb is a conservative value that we can promise to work with almost any amplicon. In many cases, significantly shorter extension times (0-5 s/kb) can be used without compromising the yield. What separates Phusion Flash DNA Polymerase from other fast polymerases is that all steps in the PCR protocol can be shortened, including annealing and denaturation. This results in extremely fast protocols as compared with any other polymerase.