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Monarch® 磁珠法 PCR & DNA 纯化试剂盒(5

μg) | NEB
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  • NEB
  • T4130
  • 2026年03月02日
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    品牌 货号 产品中文名称 产品英文名称
    NEB T4130 Monarch® 磁珠法 PCR & DNA 纯化试剂盒(5 μg) Monarch®Mag PCR & DNA Cleanup Kit (5 μg)
    货号 产品中文名称 产品英文名称 规格
    T4130L Monarch® 磁珠法 PCR & DNA 纯化试剂盒(5 μg) Monarch Mag PCR & DNA Cleanup Kit (5 µg) 400 preps
    T4130S Monarch® 磁珠法 PCR & DNA 纯化试剂盒(5 μg) Monarch Mag PCR & DNA Cleanup Kit (5 µg) 100 preps
    T4130V Monarch® 磁珠法 PCR & DNA 纯化试剂盒(5 μg) Monarch Mag PCR & DNA Cleanup Kit (5 µg) 10 preps

    产品特点
    • Magnetic bead-based kit for reliable, high-throughput PCR and DNA cleanup and purification
    • Purify up to 5 μg of DNA using a standard bind-wash-elute workflow
    • Compatible with manual and automated systems to support workflow flexibility
    • No pH monitoring needed, with our optimized buffer chemistry
    • Modified protocols available for purifying oligonucleotides, genomic DNA, and RCA products
    • Additional protocol supports varying DNA binding capacities and sample volumes

    The Monarch Mag PCR & DNA Cleanup Kit (5 μg) enables rapid and reliable purification and concentration of up to 5 μg of DNA, including both single- and double- stranded forms, from common enzymatic reactions such as PCR, restriction digestion, ligation, reverse transcription, and rolling circle amplification (RCA). Using a streamlined bind-wash-elute workflow with silica-coated magnetic beads, the kit delivers highly pure, inhibitor-free DNA ready for immediate use in downstream applications such as in vitro transcription (IVT), sequencing, restriction digestion, library construction, labeling, and other enzymatic manipulations. The magnetic bead format offers flexibility and scalability, supporting both manual and automated workflows. Additional modified protocols support varying DNA input amounts and sample volumes and enable purification of oligos, genomic DNA, and RCA products.

    The kit includes magnetic beads, optimized buffers, and reagents, all compactly packaged. The magnetic bead technology in this kit eliminates the need for centrifugation or vacuum-based processing and requires no pH monitoring, with the optimized buffer chemistry.

    Monarch kits are manufactured to ensure high quality and consistency. As with all Monarch kits, this product is designed with sustainability in mind, reducing plastic usage where possible and in the design of buffer bottles and other plastic components, while maintaining performance and reliability across a wide range of applications.

    Properties
    Purification Format Magnetic bead
    DNA Sample Type Compatibility DNA from various enzymatic reactions (restriction digestion, ligation, reverse transcription, PCR, RCA, etc.)
    dsDNA, ssDNA, circular/linear DNA, oligonucleotides, gDNA, and RCA
    Typical Recovery 70 - 90%
    DNA Purity A260/280 > 1.8 and A260/230 > 1.8
    Binding Capacity Up to 5 µg using a standard protocol. The binding capacity can be scaled up or down as needed to accommodate different sample requirements.
    Elution Volume 25–50 µl
    DNA Size Range Standard protocol: 50 bp – 25 kb
    Oligonucleotide Cleanup protocol: ssDNA ≥18 nt and dsDNA ≥14 nt
    gDNA cleanup protocol: ≥25 kb
    Compatible Downstream Applications Ligation, restriction digestion, labeling and other enzymatic manipulations, library construction and DNA sequencing, in vitro transcription template


    备注:以上仅为 T4130 的部分产品信息,如需NEB货号 T4130 的完整产品信息及相关的实验操作手册等等,请通过NEB官网查找对应的货号获取。

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    图标文献和实验
    相关实验
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      糖凝胶上检测分析。如图一所示 图一:2.2 超声破碎后,8000g,30秒,4°C,离心。将上清移入新的管子中。开始准备进行染色质免疫共沉淀(IP)。2.3 每份超声样品取50ul,这时的样品标记为INPUT,用于定量DNA浓度和作为PCR的空白对照。超声后的染色质应立刻冻入液氮中或者储存于-70°C可储存2个月。避免多次反复冻融。3检测DNA浓度1INPUT样品用于为后来的IP样品计算DNA浓度。DNA可采用PCR纯化试剂盒(加入70ul洗脱液,接着进入3.2a)或者采用酚/氯仿抽提(加入350ul

    • PCR产物的TA克隆 (DNA的胶回收和连接)

      原理】 1.DNA片段回收方法:DNA片段在适当浓度的琼脂糖凝胶中,通上一定电压进行电泳,不同大小的DNA分子由于迁移率的不同而分离开。切下带有所需DNA片段的凝胶,用冻融法、玻璃奶回收法或商品化胶回收试剂将目的片段回收纯化。 2.利用Taq酶能够在PCR产物的3’末端加上一个非模板依赖的A,而T载体是一种带有3’T突出端的载体,在连接酶作用下,可以把PCR产物插入到质粒载体的多克隆位点,可用于PCR产物的克隆和测序。

    • LightCycler通过实时荧光PCR技术进行DNA甲基化分析

      的定量。 更多有关特定CpG位点的甲基化的详细信息,可采用重亚硫酸氢盐修饰后测序分析。 LightCycler主要应用:实时荧光PCR技术进行快速准确的DNA甲基化分析 我们使用罗氏诊断公司的LightCycler®480高分辨熔解扩增试剂在LightCycler®480实时荧光PCR仪上,通过MS-HRM测定法对两种已知的经过启动子(FANCE和MGMT)甲基化的DNA修复基因的检测性能。 材料和方法 将多种细胞株的DNA样本作为检测模板。每μg的每种DNA样本都经过重亚硫酸盐修饰

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