跳转至内容
Merck

D9307

Sigma-Aldrich

JumpStart Taq DNA聚合酶

with MgCl2

别名:

hot start DNA polymerase, hot start PCR

登录查看公司和协议定价


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

正在寻找类似产品? 访问 产品对比指南

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


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

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)

商品

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.

实验方案

Whole Genome Amplification can be performed on DNA extracted in many ways. We offer many products for DNA extraction, including the GenElute™ Blood Genomic DNA Kit, GenElute Mammalian Genomic DNA Miniprep Kit and the GenElute Plant Genomic DNA M iniprep.

Blood cards provide the convenience of archiving small volumes of blood. However, many times genomic DNA from these samples is limited, This protocol provides a simple and convenient method to extract genomic DNA from a blood card. Once the DNA has been extracted, it can then be amplified using the amplification protocol

Whole blood is a common source of material used to perform genetic analysis. Many times genomic DNA isolated from whole blood samples is of low yield. This protocol is a simple method to isolate DNA from fresh or aged whole blood products. Once the DNA is isolated, it can be amplified using the GenomePlex® Whole Genome Amplification protocol.

Mycoplasma contamination of cell cultures is a serious issue impacting cell model validity. PCR testing for mycoplasma is an inexpensive, sensitive, and specific method for detecting contamination.

查看所有结果

相关内容

GenomePlex® Whole Genome Amplification is the method of extracting DNA from the animal sample. GenomePlex® products have been used to amplify genomic DNA from chicken, porcine, bovine, fish, and shrimp source.

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门