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Key Documents

Safety Information

DCAS9PROT

Sigma-Aldrich

dCas9-3XFLAG-Biotin Protein

from Streptococcus pyogenes with D10A and H840A mutations, recombinant, expressed in E. coli, 1X NLS

Synonym(s):

Cas9 D10A H840A, Dead Cas9, dCas9, catalytically inactive Cas9

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50 μG
CN¥1,033.50
250 μG
CN¥3,704.33

CN¥1,033.50


Estimated to ship onJune 24, 2025Details


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50 μG
CN¥1,033.50
250 μG
CN¥3,704.33

About This Item

UNSPSC Code:
12352202
NACRES:
NA.51

CN¥1,033.50


Estimated to ship onJune 24, 2025Details


Request a Bulk Order

recombinant

expressed in E. coli

Quality Level

Assay

≥90% (SDS-PAGE)

form

lyophilized powder

packaging

pkg of 1 kit (3 components)

shipped in

ambient

storage temp.

−20°C

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This Item
CAS9PROTESPCAS9PROPECAS9
recombinant

expressed in E. coli

recombinant

expressed in E. coli

recombinant

expressed in E. coli

recombinant

expressed in E. coli

form

lyophilized powder

form

lyophilized powder

form

lyophilized powder

form

lyophilized powder

shipped in

ambient

shipped in

ambient

shipped in

ambient

shipped in

wet ice

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

packaging

pkg of 1 kit (3 components)

packaging

pkg of 1 kit (3 components)

packaging

pkg of 1 kit (3 components)

packaging

pkg of 1 kit (4 components)

General description

Recombinant dCas9-3X FLAG-Biotin protein from Streptococcus pyogenes (~165 KD) is a ready-to-use reagent for genome engineering and genomic DNA detection, isolation and imaging experiments. When combined with target-specific guide RNAs, dead Streptococcus pyogenes Cas9 protein acts as a DNA targeting protein suitable for transfection of cell cultures, microinjection, DNA pull-down, chromatin enrichment, microbial identification and in situ DNA imaging. At the C terminus, the protein is tagged with a SV40 large T antigen nuclear localization signal (NLS) for nuclear import and both a 3XFLAG epitope and biotin for anti-FLAG®-based or streptavidin-based experiments.

Application

Functional Genomics/Target Validation/Genome Editing/Molecular Biology/Synthetic Biology/DNA detection/isolation/DNA imaging

Features and Benefits

  • Highly specific
  • Suitable for genomic DNA detection/isolation
  • Ready-to-inject/transfect

Packaging

  • pkg of 50 μg (≥ 300 pmol)
  • pkg of 250 μg (≥ 1500pmol)

Components

Each kit consists of:
  • one vial of dCas9 recombinant protein
  • one vial containing 1 mL of 1× dilution buffer
  • one vial containing 1 mL of Nuclease free water with glycerol

Principle

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 protein can then be programmed with a gRNA and directed to bind at a desired sequence of DNA.

Reconstitution

Lyophilized dCas9 protein should be resuspended in the Reconstitution solution provided to desired concentration. Gently tap tube to completely dissolve lyophilized powder, incubate for 10 minutes on ice, and spin tube to bring material to bottom of tube.

Other Notes

Use our CRISPR Selection Tool to order gRNA

Check out our other MISSION® Cas9 Proteins at SigmaAldrich.com/CRISPRproteins

Legal Information

3xFLAG is a trademark of Sigma-Aldrich Co. LLC
FLAG is a registered trademark of Merck KGaA, Darmstadt, Germany
MISSION is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

10 - Combustible liquids

Regulatory Information

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Matthew D Newton et al.
Methods in molecular biology (Clifton, N.J.), 2478, 349-378 (2022-09-06)
The discovery of CRISPR/Cas9 as an easily programmable endonuclease heralds a new era of genetic manipulation. With this comes the prospect of novel gene therapy approaches, and the potential to cure previously untreatable genetic diseases. However, reports of spurious off-target

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