Clontech/Long ssDNA for knockins/25 Rxns/632644

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Long ssDNA for gene knockin experiments

CRISPR/Cas9 and other gene editing tools have been successfully used for obtaining knockout mutations, but knockin mutations have proven to be much harder to introduce. A major challenge has been the production and delivery of the repair template along with the Cas9-sgRNA ribonucleoprotein complex.

CRISPR/Cas9 and other gene editing tools have been successfully used for obtaining knockout mutations, but knockin mutations have proven to be much harder to introduce. A major challenge has been the production and delivery of the repair template along with the Cas9-sgRNA ribonucleoprotein complex.

Although single-stranded DNA (ssDNA) repair templates have recently been shown to have several advantages over double-stranded DNA (dsDNA) templates, the usefulness of long ssDNA templates is limited due to the difficulty and cost of producing them. The Guide-it Long ssDNA Strandase Kit is designed to produce a long ssDNA oligo of up to 5 kb in length for use as a repair template in knockin experiments using CRISPR/Cas9 or other gene editing tools. This kit provides a simple method for converting a dsDNA PCR product into ssDNA by selectively digesting either the sense or the antisense strand. The kit contains sufficient reagents to create 50 ssDNA strands (25 pairs of sense and antisense strands).

Benefits of using ssDNA as a template over dsDNA:

  • Drastically reduced tendency to randomly integrate into the genome, resulting in an improved gene editing efficiency
  • Low cytotoxic response to ssDNA template delivery
  • No expression from nonintegrated templates, making identification of correctly edited clones significantly easier
  • NOTE: The Guide-it Long ssDNA Production System includes a NucleoSpin Gel and PCR Clean-up kit to purify the strandase reaction before using it for gene editing
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美国Clontech www.clontech.com www.takara.com.cn www.takara-bio.com www.takara.co.jp 2005年7月1日,日本最大的生物工程公司TaKaRa公司据说花费了6千万美元成功此收购计划已经于2005年8月底完成,Clontech已成为TaKaRa全资子公司。美国Clontech是1984年由华人方瑞贤创立的,一度曾经是众多海外华人的骄傲。因为方瑞贤创立的是全美第一家,也是建立了最大的分子生物公司,更重要的是Clontech建立了生物技术中建立基因文库的模式。在Clontech被BD收购时已有四百名员工,包括六十五位博士,拥有五十多个专利,产品已达两千多个,堪称全球数一,数二的基因库,提供全球三十多个国家基因实验室或学术界做研究之用。该公司有曾于预期四,预期五,预期八及预期九年被圣荷西及旧金山商业报纸选为一百个成长速度的私人公司。Clontech公司一直锐意进取,其开发的产品多次获得全美R&D100金奖。产品范围包括基因识别,基因表达,基因功能研究,大家熟悉的Smart Race,Altas DNA矩阵,SSH消减杂交,MTN膜,多色荧光蛋白载体,MatchMaker酵母双杂交系列也在其中。TaKaRa公司于1979年年从生产限制性内切酶起步,首先将PCR技术引入日本市场,并逐渐成为日本生命科学研究领域领先的公司.TaKaRa在2004年财政年度试剂销售达到118亿日元(1十亿美元左右),其中85%的收益来自于日本本土市场,其他有部分来自于中国等亚洲市场。此次收购会给Takara带来以下收益:极大地丰富Takara原来的产品线;迅速扩大TaKaRa在欧美市场的份额,因为Clontech 70%以上的销售是来自于欧美,而Takara 85%的收益来自于日本本土市场。本次收购将全面扩展日本产品在欧美的销售。另外宝将整合并加强日本本土和位于美国的Clontech公司研发部,加快产品的开发,提高宝在全球生命科学研究市场的份额。