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当前位置: 首页 > 产品中心 > > Bioclone/ BcMag™ Oligo-dT Magnetic Beads/4 ml/MMS102
商品详细Bioclone/ BcMag™ Oligo-dT Magnetic Beads/4 ml/MMS102
Bioclone/ BcMag™ Oligo-dT Magnetic Beads/4 ml/MMS102
Bioclone/ BcMag™ Oligo-dT Magnetic Beads/4 ml/MMS102
商品编号: MMS102
品牌: Bioclone Inc
市场价: ¥7600.00
美元价: 4560.00
产地: 美国(厂家直采)
公司:
产品分类: 其他
公司分类:
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

Poly(A)+ RNA extraction is a crucial step in many downstream applications, such as qRT-PCR, RNA sequencing, and microarray analysis. However, traditional methods for RNA isolation, such as phenol-chloroform extraction, can be time-consuming, labor-intensive, and hazardous to human health due to the use of organic solvents. Therefore, there is an urgent need for a rapid and efficient method for poly(A)+ RNA extraction that ensures the isolation of intact mRNA molecules.

The BcMag™ Quick mRNA Purification Kit is a novel tool designed to extract intact poly(A)+ RNA from cells and tissue samples. Unlike other methods that use chemical solvents like phenol, this kit uses Oligo-d(T)25 attached to 1µm paramagnetic beads to bind the poly(A)+ RNA directly. This makes it possible to manually process multiple samples or adapt the process for high-throughput automated applications. The use of magnetic separation technology allows for the elution of intact mRNA in small amounts, which means that the poly(A)+ transcripts do not need to precipitate in the eluent. In less than an hour, this method can produce intact poly(A)+ RNA that is fully representative of the original sample’s mRNA population.

Workflow: Simplified and User-Friendly

The purification with magnetic beads is a straightforward and user-friendly process. First, mix the beads with the cell lysates and incubate them with continuous rotation for a sufficient time. The beads remain suspended in the sample solution during mixing, allowing the mRNA to bind to oligo-dT magnetic beads. Ribosomal RNA and tiny RNA molecules (transfer RNA, microRNA, small nucleolar RNA, and small cytoplasmic RNA) do not adhere to the beads and are eliminated. After incubation, only polyadenylated RNA species (mRNA) are collected and separated from the sample using a magnet rack. Then the ultrapure mRNAs are eluted and used in downstream applications.

Workflow for quick mRNA purification

Advantages of BcMag™ Quick mRNA Purification Kit

High Yield: The kit produces a high yield of poly(A)+ RNA from various sources, such as cultured cells, tissues, and blood.

Fast and Efficient: The entire process takes less than an hour, making it a fast and efficient method for poly(A)+ RNA extraction.

Compatible with Automated Systems: The process is adaptable to automated systems, allowing for high-throughput applications.

Easy-to-Use: The protocol is straightforward and user-friendly, making it accessible to a broad range of researchers.

Intact mRNA: The BcMag™ Quick mRNA Purification Kit ensures the isolation of intact mRNA molecules, which is crucial for downstream applications such as qRT-PCR and RNA sequencing.

Advantages of BcMag™ Quick mRNA Purification Kit

The purified poly(A)+ RNA obtained from the BcMag™ Quick mRNA Purification Kit can be used in various downstream applications, such as:

qRT-PCR: The kit provides high-quality RNA for qRT-PCR analysis, which is a widely used technique for gene expression analysis.

RNA Sequencing: The kit produces high-quality RNA suitable for RNA sequencing, which allows for the identification of novel transcripts and alternative splicing events.

Microarray Analysis: The kit produces high-quality RNA suitable for microarray analysis, which allows for the simultaneous analysis of the expression of thousands of genes.

Learn More

Instruction Manual

MSDS

DNA & RNA Purification Related Products →

General Reference

1.

Ferrier DC, Shaver MP, Hands PJW. Micro- and nano-structure-based oligonucleotide sensors. Biosens Bioelectron. 2015 Jun 15;68:798-810.

2.

Sethi D, Gandhi RP, Kuma P, Gupta KC. Chemical strategies for immobilization of oligonucleotides. Biotechnol J. 2009 Nov;4(11):1513-29.

3.

Zuo P, Ye BC. A novel immobilization strategy using oligonucleotide as linker for small molecule microarrays construction. Biosens Bioelectron. 2008 Jun 15;23(11):1694-700.

品牌介绍
Bioclone的用于学术研究和治疗应用的重组蛋白/ DNA的数量已大大增加。然而,成功的重组蛋白表达取决于许多因素,例如密码子偏好性,RNA二级结构,异源表达系统中的GC含量。越来越多的实验结果证明,与预优化相比,取决于不同的基因,表达水平显着提高,从两倍提高到一百倍。Bioclone开发了一个独特的专有技术平台,并生成了超过14,000个人工合成的,经过密码子优化的cDNA / DNA克隆(克隆在大肠杆菌表达载体中,图1)和重组蛋白(在大肠杆菌酵母中生产)。Bioclone为所有cDNA克隆和重组蛋白生产提供即用型和基于客户的服务。特别设计和合成了数十万种重组蛋白和密码子优化的cDNA (DNA开放阅读框)。  密码子优化的cDNA / DNA:    产生更高产量的重组蛋白。将cDNA / DNA 克隆克隆到具有6x His -tag的大肠杆菌表达载体中,可立即用于重组蛋白生产。可以使用作为验证的RNAi的功能由于在其〜30%差的RNAi的援助cDNA序列时相比原的cDNA / DNA 。Bioclone 还提供客户服务克隆中的cDNA插入NY 所需的客户向量小号。重组蛋白:重组蛋白C 在N末端或C末端具有6x His-tag重组蛋白P roduced在大肠杆菌或小号F9昆虫细胞。  provid 我纳克准备使用的重组蛋白和p rotein点播服务的所有cDNA克隆。通过SDS-PAGE 测定的重组蛋白纯度> 90%。ř ecombinant蛋白应用:Western印迹,ELISA 或可以用于其它应用。  cDNA克隆和重组蛋白包括:我nfection疾病抗原(病毒,细菌,寄生虫,细菌毒素),抗过敏的蛋白质,细胞因子,   激酶,磷酸酶,信号转导,   干细胞和发展,神经科学, 药物   metabollism,普通的病,转录因子,癌症和更重组蛋白质和克隆是g 还是机翼.......