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D9307

Sigma-Aldrich

JumpStart Taq DNA聚合酶

with MgCl2

同義詞:

hot start DNA polymerase, hot start PCR

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About This Item

MDL號碼:
分類程式碼代碼:
12352204
NACRES:
NA.55

品質等級

形狀

liquid

用途

sufficient for 1500 reactions
sufficient for 250 reactions
sufficient for 50 reactions

特點

dNTPs included: no
hotstart

濃度

2.5 units/μL

技術

PCR: suitable

顏色

colorless

輸入

purified DNA

適合性

suitable for PCR

應用

agriculture

運輸包裝

wet ice

儲存溫度

−20°C

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一般說明

JumpStart Taq DNA聚合酶是Sigmas高性能Taq DNA聚合酶和JumpStart Taq抗体的混合物。Taq DNA聚合酶活性通过将该酶与JumpStart Taq抗体(Taq DNA聚合酶的中和性单克隆抗体)结合而失活。抗体失活为热启动PCR提供了一种简单、有效的方法。PCR过程中,JumpStart Taq DNA聚合酶在低温(室温)下不活跃,当温度在第一步循环变性中升高到70℃以上,复合体解离,聚合酶完全激活。

應用

JumpStart Taq DNA聚合酶已用于:
  • 扩增不同大小的DNA库
  • 在甲基化特异性、定量实时聚合酶链反应(MS-qPCR)中,确定BRCA1启动子甲基化状态
  • 通过PCR扩增全长HIF1β,生成质粒
  • 用于需要降低非特异性扩增的PCR扩增
  • 用于多重PCR
  • 用于降低引物二聚体

特點和優勢

  • 降低非特异性扩增
  • 提高PCR特异性及产量
  • 减少与手动或蜡热启动方法相关的设置时间担忧
  • 低于1分钟的激活时间

包裝

JumpStart Taq DNA聚合酶是以10x反应缓冲液形式提供的,并可选择是否含有MgCl2。 不含镁的10x缓冲液还包含单独一管的25 mM MgCl2用于优化。
本品为含15 mM MgCl2的10×反应缓冲液

其他說明

Sigma的JumpStart Taq DNA聚合酶是一种抗体失活的热启动酶,设计用于最大限度降低非特异性扩增并同时提高靶标的产量。 一旦反应温度达到 70°C,Taq DNA聚合酶活性就会得到恢复,使得PCR具有更高的特异性和产量。这种抗体-酶复合物可实现简单便捷的设置,并相对于手动热启动技术具有更低的污染风险。 该酶还可以被加入到预混液制备中,从而实现反应之间更高的一致性。
可访问www.sigma-aldrich.com/hotstart查看更多关于JumpStart Taq酶的详细信息。

單位定義

在74 °C,一单位的酶可以在30分钟内将10 nmol的总dNTP插入至可酸沉淀的DNA中。

法律資訊

本产品的使用受到如下一项或多项美国专利及其对应的美国境外专利声明保护:US 8,404,464及US 7,972,828. 购买本产品,即相当于依照境外的专利声明获得了一份受限制、不可转让的使用许可。

抗体授权用于在美国专利5,338,671和5,587,287及其在其他国家相应专利保护下的体外研究用途。
JumpStart is a trademark of Sigma-Aldrich Co. LLC

儲存類別代碼

10 - Combustible liquids

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號,寫有 ‘Lot’或‘Batch’.。

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您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

High quality bisulfite sequencing using nanogram amounts of genomic DNA
Sun J, et al.
International journal of biochemistry and biotechnology, 2, 449-456 (2013)
Ning Li et al.
Methods (San Diego, Calif.), 52(3), 203-212 (2010-05-01)
There are numerous approaches to decipher a whole genome DNA methylation profile ("methylome"), each varying in cost, throughput and resolution. The gold standard of these methods, whole genome bisulfite-sequencing (BS-seq), involves treatment of DNA with sodium bisulfite combined with subsequent
Memory T Cells Expressing an NKG2D-CAR Efficiently Target Osteosarcoma Cells.
Lucía Fernández et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 23(19), 5824-5835 (2017-07-01)
Whole genome DNA methylation analysis based on high throughput sequencing technology
Li N, et al.
Methods, 52(3), 203-212 (2010)
Disruption of Abi1/Hssh3bp1 expression induces prostatic intraepithelial neoplasia in the conditional Abi1/Hssh3bp1 KO mice
Xiong X, et al.
Oncogenesis, 1(9), e26-e26 (2012)

文章

Learn about the history of the polymerase chain reaction (PCR), from the basic principles that proceeded its discovery to the awarding of a Nobel Prize for Chemistry and more recent developments such as real-time PCR (qPCR) and digital PCR.

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