来宝网Logo

热门词:生物显微镜 水质分析仪 微波消解 荧光定量PCR 电化学工作站 生物安全柜

现在位置首页>技术资料首页>行业动态>促销与活动>TonkBio cDNA 位列前茅链合成试剂盒免费试用

TonkBio cDNA 位列前茅链合成试剂盒免费试用

上海同科生物科技有限公司2017年10月23日 10:40 点击:1258

Storage and Stability

Store all system components at -20 for one year.

Description

The TonkBioTM First Strand cDNA Synthesis Kit for RT-PCR is optimized to efficient synthesize first strand cDNA from mRNA or total RNA templates. The kit uses M-MLV reverse transcriptase with lower RNase H activity, which avoids degradation of RNA when RNA-DNA hybrid forms in the progress of cDNA synthesis. It is suitable for synthesis of cDNA up to 9 kb.

The cDNA products could be used directly in a variety of downstream applications, including PCR, qPCR, gene clone.

Caution

1. For research use only.

2. Use RNase-free reagents during RNA extraction and cDNA synthesis process.

3. NO repeated freezing and thawing RNA. RNA should be dissolved in ice-water mixture.

4. The reverse transcription reaction products should be stored at -20℃.

5. Wear gloves when handling RNA and all reagents as skin is a common source of RNases.

Example of application

TonkBio-First-Chain-cDNA-Synthsis-Kit-700-447.jpg

Troubleshooting Guide

1. NO or low product of RT PCR

1Degradation of RNA template. RNA Purity and integrity is important to obtain full length cDNA. Users have to make gel electrophoresis detection to ensure no degradation occurred. And avoid repeated freezing and thawing RNA.

2Low concentration of RNA template. Trace amount of agents used in RNA purification may remain in solution and inhibit cDNA synthesis. Suggest to wash RNA with 75% ethanol ( prepared by DEPC water) carefully.

3Incorrect primers. Select random primers or specific primers instead of OligodT primer with bacterial RNA or RNA without a poly A tail.

4GC rich template. If the RNA template is GC-rich or contains secondary structures, choose random primers and increase the reaction temperature of transcription up to 55℃.

2. RT-PCR product longer than expected

RNA sample is contaminated with DNA. To avoid genomic DNA contamination, User could use DNase I to digest RNA sample before transcription or design primers on exon-intron boundaries.

3. Product of RT-PCR in negative control

RNA template is contaminated with DNA. Perform DNaseI digestion prior reverse transcription.

免费试用说明:

1.运费:申请机构(单位)无需承担试用装的运输费用

2.发货时间:申请审核通过后,协商发货时间;

3.申请要求:申请实验室有相应实验,能够近期开展实验;

4.其它说明:请提供试用报告,谢谢配合!


(来源: 上海同科生物科技有限公司


全年征稿 / 资讯合作

联系邮箱:kefu@labbase.net

版权与免责声明

  • 凡本网注明“来源:来宝网”的所有作品,版权均属于来宝网,转载请必须注明来宝网, //www.next-search.com,违反者本网将追究相关法律责任。
  • 本网转载并注明自其它来源的作品,目的在于传递更多信息,并不代表本网赞同其观点或证实其内容的真实性,不承担此类作品侵权行为的直接责任及连带责任。其他媒体、网站或个人从本网转载时,必须保留本网注明的作品来源,并自负版权等法律责任。
  • 如涉及作品内容、版权等问题,请在作品发表之日起一周内与本网联系,否则视为放弃相关权利。