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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
RapidOut DNA Removal Kit
- 规格:
50 preps
描述
Thermo Scientific RapidOut DNA Removal Kit rapidly and safely removes genomic DNA from total RNA and mRNA preparations. Complete digestion of DNA and safe removal of DNase I from the digestion reaction is ensured without RNA damaging steps, such as heating or organic extraction. First, the RNA sample is treated with recombinant RNase-free DNase I to levels below the limit of detection by routine PCR. DNase I is safely removed subsequently using proprietary DNase Removal Reagent (DRR).DRR efficiently binds DNase I and the complex is collected at the bottom of the tube by centrifugation. The purified RNA is collected as a supernatant. The RNA after RapidOut procedure is free from DNA contamination and free of DNase I. It is ready to use in different applications including end-point or real-time RT-PCR, cloning, microarrays, and Northern blotting.
Highlights
• Efficient—complete ds and ssDNA digestion and proprietary technology for DNase I removal
• Rapid—single step sufficient for complete DNase I removal
• Safe—no need for toxic organic extractions or RNA-damaging heating steps
Applications
Main Applications
• RNA isolation and RNA analysis, particularly RT-qPCR and RT-PCR (customers performing expression analysis of low transcription level genes.
• Customers performing ds-cDNA synthesis from total RNA preps.
Other applications
• Elimination of DNA from RNA for microinjections and transfection.
• Elimination of DNA from RNA prior microarray analysis.
• Elimination of DNA from RNA prior Northern blot analysis.
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文献和实验• 以96孔板方式,从同一个细胞或组织样本中同时纯化基因组 DNA和总RNA • 处理 96 个样本,只需不到60 分钟 • 从同一样本中纯化高品质的基因组DNA和总RNA • 96孔板方式,高效的操作流程 • 高度标准化的操作流程 • 高重复性的DNA和RNA产量 Product description The AllPrep DNA/RNA 96 Kit is well suited for high
FDA、SFDA对重组蛋白、vero细胞疫苗等生物制品的DNA残留均有严格要求,近年来包括大牌进口产品在内的狂犬疫苗DNA残留超标问题,引起了社会和业界的广泛关注。为什么一个看似简单的问题,却给众多专业人员带来如此大的困扰?一方面是由于DNA超强的化学稳定性,另一方面是由于DNA其带有大量的电荷易与其他生物大分子结合从而产生聚集(吸附)、包裹作用而难以完全除去。DNA的去除方法主要有层析、膜过滤、离心、沉淀、酶解等方法。这里对工业上应该最广泛和有效的离子交换层析、鱼精蛋白沉淀、酶解三类方法进行
Removal of Ethidium Bromide from DNA by Extraction with Organic Solvents Joseph Sambrook Peter Maccallum Cancer Institute and The University of Melbourne, Australia David W
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