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: 保靖县| 宜阳县| 洛扎县| 大洼县| 页游| 普格县| 义马市| 新邵县| 屏东县| 朝阳区| 渭南市| 郎溪县| 华池县| 广安市| 兰溪市| 霍山县| 淄博市| 靖远县| 津南区| 金寨县| 吴堡县| 玉树县| 平遥县| 香河县| 阿拉尔市| 巩留县| 伊吾县| 三亚市| 项城市| 晋城| 从化市| 陈巴尔虎旗| 微山县| 南通市| 姜堰市| 阜城县| 隆安县| 南华县| 吉木乃县| 凌云县| 彭泽县|