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Key Documents

DCAS9P

Sigma-Aldrich

Dead Cas9 plasmid

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About This Item

分類程式碼代碼:
41106609
NACRES:
NA.51

重組細胞

expressed in E. coli

形狀

liquid

包裝

vial of 50 μL

濃度

20 ng/μL in TE buffer; DNA (1μg of plasmid DNA)

應用

CRISPR

啟動子

Promoter name: CMV

選擇

kanamycin

運輸包裝

dry ice

儲存溫度

−20°C

一般說明

This product is an expression plasmid that utilizes the CMV promoter for strong transient expression of Dead Cas9 (CMV-dCas9). The dCas9 expression plasmid is one part of a two part CRISPR system with individual dCas9 and gRNA expression vectors.

To order gRNA in any format click here

應用

Functional Genomics/Target Validation
  • Proxy CRISPR
  • Suitable for genomic DNA detection

特點和優勢

  • Highly specific
  • Sequence verified
  • Ready to use purified plasmid DNA

原則

CRISPR/Cas systems are employed by bacteria and archaea as a defense against invading viruses and plasmids. Recently, the type II CRISPR/Cas system from the bacterium Streptococcus pyogenes has been engineered to function in eukaryotic systems using two molecular components: a single Cas9 protein and a non-coding guide RNA (gRNA).The Cas9 endonuclease can be rendered inactive (dCas9) with mutations to the two protein domains, RuvC and HnH (D10A and H840A respectively), which are responsible for nuclease activity. The nuclease deficient protein can then be programmed with a gRNA and directed to bind at a desired sequence of DNA. Variants of programmable endonucleases are often unable to cleave a large number of the targets that are efficiently cleaved by canonical SpCas9 in human cells. Cotargeting dead Cas9 may alter local chromatin structures and render otherwise inaccessible target sites now accessible and cleavable by alternative nucleases such as type II-B FnCas9, type II-C CjCas9 and NcCas9 and type V FnCpf1.

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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存取文件庫

Targeted activation of diverse CRISPR-Cas systems for mammalian genome editing via proximal CRISPR targeting.
Chen, F. et al.
Nature Communications, 8 (2017)

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