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主要产品:NEB、内切酶、基因表达、RNAi DNA修饰酶、各种载体、 Marker 、引物、测序 等等
℡ 4000-520-616
℡ 4000-520-616
NEB/HiScribe® T7 High Yield RNA Synthesis Kit/50 reactions/E2040S
产品编号:E2040S
市  场 价:¥0.00
场      地:美国(厂家直采)
产品分类: 分子类>核酸酶类>其他>
联系QQ:1570468124
电话号码:4000-520-616
邮      箱: info@ebiomall.com
美  元  价:待定
品      牌: NEB
公      司:New England Biolabs
公司分类:
NEB/HiScribe® T7 High Yield RNA Synthesis Kit/50 reactions/E2040S
商品介绍
The HiScribe T7 High Yield RNA Synthesis Kit is an extremely flexible system for in vitro transcription of RNA using T7 RNA Polymerase. The kit allows for synthesis many kinds of RNA including internally labeled and co-transcriptionally capped transcripts.RNA synthesized from the kit is suitable for many applications including RNA structure and function studies, ribozyme biochemistry, probes for RNase protection assays and hybridization based blots, anti-sense RNA and RNAi experiments, microarray analysis, microinjection, and in vitro translation and RNA vaccines.The kit contains sufficient reagents for 50 reactions of 20 μl each. Each standard reaction yields up to 180 μg of RNA from 1 μg control template. Each kit can yield up to 9 mg RNA. For 32P labeling, the kit contains enough reagents for 100reactions of 20 μl each.Materials Not Included:
  • DNA Template: The DNA template must be linear and contain the T7RNA Polymerase promoter with correct orientation in relation to target sequence to be transcribed.
  • 3′-O-Me-m7G(5′)ppp(5′)G RNA Cap Structure Analog (NEB #S1411)
  • m7G(5′)ppp(5′)G RNA Cap Structure Analog (NEB #S1404)
  • m7G(5′)ppp(5′)A RNA Cap Structure Analog (NEB #S1405)
  • G(5′)ppp(5′)A RNA Cap Structure Analog (NEB #S1406)
  • G(5′)ppp(5′)G RNA Cap Structure Analog (NEB #S1407)
  • Modified-NTP: Biotin-, Fluorescein-, Digoxigenin-, or Aminoallyl-NTP
  • Labeling: [α-32P] labeled ribonucleotide (800-6,000 Ci/mmol)
  • General: 37°C incubator or PCR machine, nuclease-free water
  • DNase I: DNase I (RNase-free) (NEB #M0303)
  • Purification: Buffer- or water-saturated phenol/chloroform, ethanol and 3 M sodium acetate, pH 5.2, spin columns
  • Gel Analysis: Gels and running buffers, gel apparatus, power supply
Figure 1. Transcription by T7 RNA PolymeraseFigure 1. Transcription by T7 RNA Polymerase
Figure 2. Time course of standard RNA synthesis from three DNA templatesFigure 2. Time course of standard RNA synthesis from three DNA templates
Reactions were incubated at 37°C in a PCR machine. Transcripts were purified by spin columns and quantified on NanoDrop™ Spectrophotometer.
Figure 3. Effect of template amount on RNA yieldFigure 3. Effect of template amount on RNA yield
Standard reactions were incubated at 37°Cin a PCR machine for 2 hours. Transcripts were purified by spin columns and quantified on NanoDrop™ Spectrophotometer.
Figure 4: Improved RNA yield and integrity from extended duration transcription reactionsFigure 4: Improved RNA yield and integrity from extended duration transcription reactions
reactions were assembled, in duplicate, according to the manufacturers’ suggested protocols using 3 ng of dsDNA template encoding a 1.8 kb RNA, and incubated at 37°C for 16, 24 and 40 hours. At each time point, the corresponding tubes were transferred to -20°C to stop the reaction. Transcription reactions were column purified after the last time point.(A) Transcript yield – After column purification, RNA concentration was measured using a NanoDrop spectrophotometer and total RNA yield was calculated. These data demonstrate that a substantially higher yield of RNA was synthesized using the HiScribe T7 High Yield RNA Synthesis Kit as compared to the competitor’s kit.(B) Transcript integrity – 150 ng of column purified RNA was run a 1.2% denaturing agarose gel, stained with ethidium bromide and visualized by UV fluorescence. The data demonstrate greatly improved transcript integrity after extended duration RNA synthesis reactions using the HiScribe T7 High Yield RNA Synthesis Kit as compared to the competitor’s kit.
This product is related to the following categories:
RNA Synthesis Products
This product can be used in the following applications:
RNA Labeling,
In vitro Transcription for RNA Synthesis
品牌介绍

NEB公司成立于二十世纪七十年代中期,拥有众多经验丰富的科学家,是生产生命科学试剂的领导者。目前,NEB为基因组研究提供最齐全的重组酶和天然酶,并且公司业务范围已延伸至蛋白质组学和药品开发领域。回顾三十余年来的历程,NEB公司作为先驱公司之一,为促进生物科技工业的发展做出了巨大的贡献。NEB美国总部乔 迁新址后拥有最尖端的设备,有一座现代化的发酵中心及设备齐全的实验室,这些实验室主要用于产品生产、质量监控、 产品开发和基础科研之用。作为首批以商业规模生产限制性内切酶的公司之一,NEB一直专注于内切酶的研究,并保持 业内领先水平。NEB公司一贯坚持以科学为本的原则,公司生产的试剂因其高质量、高性价比享誉世界。NEB(北京)有限公司 New England Biolabs (Beijing) LTD. NEB(北京)有限公司New England Biolabs (Beijing) LTD. 为美国New England Biolabs, Inc.在华投资兴建的独资子公司,负责处理其在中国内地及香港地区的全部业务,同时承担部分新产品的研发工作。纽英伦生物技术(北京)有限公司成立于2001年11月,为中国生命科学研究者提供一流的产品和专业的技术服务,促进国内外生命科学学术交流,与中国科研工作者一起将中国推入到二十一世纪生命科学的前沿中去。

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