国产精品久久久久久永久牛牛,55国产福利在线视频,成人午夜精品视频在线观看

目錄產品 » GenCRISPR™/Cas9 基因編輯相關產品 » GenCRISPR™ Cas9 Enzymes » GenCrispr NLS-Cas9-NLS Nuclease
GenCrispr NLS-Cas9-NLS Nuclease

In vitro DNA cleavage assay with GenCrispr NLS-Cas9-NLS nuclease
Reactions were set up according to recommended conditions, and cleavage products were resolved on a 1% agarose gel. Input DNA is EcoRV-linearized pUC57 plasmid DNA

GenCrispr NLS-Cas9-NLS Nuclease

GenCrispr NLS-Cas9-NLS nuclease is the recombinant Streptococcus pyogenes Cas9 (wt) protein with a nucleic localization signal (NLS) on both N and C terminal, which can be used for genome editing by inducing site-specific DNA double stranded breaks. Cas9 protein forms a very stable ribonucleoprotein (RNP) complex with the guide RNA (gRNA) component of the CRISPR/Cas9 system, which can localize to the nucleus immediately once entering the cell with the guide of the NLS. Compared with the mRNA or plasmid systems, transcription and translation processes are not required. This DNA-free system avoids the risk of inserting foreign DNA into the genome, which can be quite useful for gene editing-based disease therapy. Our highly pure and active Cas9 nuclease meets all of the researcher′s requirements (e.g. in vitro cleavage assay, RNP complex transfection, micro injection). Product Source: GenCrispr NLS-Cas9-NLS is produced by expression in an E. coli strain carrying a plasmid encoding the Cas9 gene from Streptococcus pyogenes with a double-ends nuclear localization signal (NLS). Key features: DNA-free: no external DNA added to system. High cleavage efficiency: Double NLS ensures the efficient entry of Cas9 protein into nuclei. Low off target: transient expression of Cas9 nuclease. Time-saving: no need for transcription and translation. With this Cas9 Nuclease, you can: Screening the highly efficient and specific targeting gRNAs using in vitro DNA cleavage. In vivo gene editing combined with specific gRNA by electroporation or injection.
Z03389
詢價

聯系我們
Description

GenCrispr NLS-Cas9-NLS nuclease is the recombinant Streptococcus pyogenes Cas9 (wt) protein with a nucleic localization signal (NLS) on both N and C terminal, which can be used for genome editing by inducing site-specific DNA double stranded breaks. Cas9 protein forms a very stable ribonucleoprotein (RNP) complex with the guide RNA (gRNA) component of the CRISPR/Cas9 system, which can localize to the nucleus immediately once entering the cell with the guide of the NLS. Compared with the mRNA or plasmid systems, transcription and translation processes are not required. This DNA-free system avoids the risk of inserting foreign DNA into the genome, which can be quite useful for gene editing-based disease therapy. Our highly pure and active Cas9 nuclease meets all of the researcher´s requirements (e.g. in vitro cleavage assay, RNP complex transfection, micro injection).

Product Source: GenCrispr NLS-Cas9-NLS is produced by expression in an E. coli strain carrying a plasmid encoding the Cas9 gene from Streptococcus pyogenes with a double-ends nuclear localization signal (NLS).

Key features:

  • DNA-free: no external DNA added to system.
  • High cleavage efficiency: Double NLS ensures the efficient entry of Cas9 protein into nuclei.
  • Low off target: transient expression of Cas9 nuclease.
  • Time-saving: no need for transcription and translation.

With this Cas9 Nuclease, you can:

  1. Screening the highly efficient and specific targeting gRNAs using in vitro DNA cleavage.
  2. In vivo gene editing combined with specific gRNA by electroporation or injection.

Note

1000 nM is equal to 160 ng/ul.

Storage & Stability GenCrispr NLS-Cas9-NLS nuclease is supplied with 1 x storage buffer (10 mM Tris, 300 mM NaCl, 0.1 mM EDTA, 1 mM DTT, 50% Glycerol pH7.4 at 25℃) and recommended to be stored at -20℃.

  • GenCrispr NLS-Cas9-NLS Nuclease
  • GenCrispr NLS-Cas9-NLS Nuclease

    In vitro DNA cleavage assay with GenCrispr NLS-Cas9-NLS nuclease
    Reactions were set up according to recommended conditions, and cleavage products were resolved on a 1% agarose gel. Input DNA is EcoRV-linearized pUC57 plasmid DNA


喜歡新升級的網站嗎?

討厭

不喜歡

一般

喜歡

非常喜歡

*
    主站蜘蛛池模板: 舒城县| 乌拉特后旗| 泗洪县| 九龙坡区| 太保市| 宝兴县| 班戈县| 廉江市| 仪陇县| 海安县| 珲春市| 即墨市| 卫辉市| 抚宁县| 甘南县| 六枝特区| 耿马| 贵南县| 千阳县| 玉门市| 阿巴嘎旗| 黄平县| 宁乡县| 昌吉市| 乌兰察布市| 金乡县| 大安市| 城市| 凌云县| 胶州市| 靖安县| 绥棱县| 宣威市| 青田县| 台中市| 灵璧县| 民乐县| 根河市| 巴青县| 扎赉特旗| 新疆|