Both Cas9-GFP and eSpCas9-GFP exhibit similar transfection rates in terms of efficiency. However, in terms of editing activity, Cas9-GFP has greater activity than eSpCas9-GFP. The eSpCas9-GFP variant, while more specific, compromises on activity, particularly noticeable with difficult-to-edit targets. The eSpCas9 variant is suitable when high specificity is a priority, the target is relatively easy to modify, and the model system can effectively recover after transfection to enable the isolation of a decreased population of edited cells.
ECAS9GFPPR
eSpCas9-GFP Protein
from Streptococcus pyogenes with mutations conferring enhanced specificity, fused with enhanced GFP, recombinant, expressed in E. coli, 3X NLS
Sinonimo/i:
eSpCas9-EGFP, eSpCas9-GFP
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50 μG
CHF 283.00
250 μG
CHF 566.00
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Cambia visualizzazione
50 μG
CHF 283.00
250 μG
CHF 566.00
About This Item
Codice UNSPSC:
12352202
NACRES:
NA.51
Prodotti consigliati
Ricombinante
expressed in E. coli
Saggio
≥90% (SDS-PAGE)
Stato
lyophilized powder
Confezionamento
pkg of 1 kit (3 components)
Gene reporter
GFP
Condizioni di spedizione
wet ice
Temperatura di conservazione
−20°C
Descrizione generale
Recombinant enhanced specificity Cas9-GFP protein from Streptococcus pyogenes (~192 KD) is a ready-to-use reagent for genome engineering experiments. When combined with target-specific guide RNAs, eSpCas9-GFP protein will act as a targeted nuclease suitable for transfection of cell cultures and for the accelerated development of genetically-modified animals via one-cell embryo injection.
An N-terminally fused enhanced green fluorescent protein with an excitation peak at 488 nm and emission peak at 509 nm allows for visualization of transfected RNP complex in addition to utility in flow cytometry applications. The protein also contains three varied nuclear localization sequences postioned for optimal activity.
An N-terminally fused enhanced green fluorescent protein with an excitation peak at 488 nm and emission peak at 509 nm allows for visualization of transfected RNP complex in addition to utility in flow cytometry applications. The protein also contains three varied nuclear localization sequences postioned for optimal activity.
Applicazioni
- Functional Genomics
- Target Validation
- Genome Editing
- Fluorescence Microscopy
- Flow Cytometry
Caratteristiche e vantaggi
- Enhanced specificity compared to wild type Cas9
- Highly active
- Ready-to-inject/transfect
Confezionamento
pkg of 50 μg ( ≥260 pmol )
pkg of 250 μg ( ≥1300 pmol)
pkg of 250 μg ( ≥1300 pmol)
Componenti
Each kit consists of:
- one vial of lyophilized eSpCas9-GFP recombinant protein
- one vial containing 1 mL of 1x dilution buffer
- one vial containing 1 mL of nuclease-free water with glycerol
Principio
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 programmed with a single gRNA, directing a DNA double-strand break (DSB) at a desired genomic location. Similar to DSBs induced by zinc finger nucleases (ZFNs), the cell then activates endogenous DNA repair processes, either non-homologous end joining (NHEJ) or homology-directed repair (HDR), to heal the targeted DSB.
Newly engineered eSpCas9 (1.1) enables the efficient targeted gene editing of established CRISPR systems with the benefit of reduced off-target effects. Point mutations (K848A/K1003A/R1060A) in the chromosome-binding motif of SpCas9, as described by Slaymaker, et al., provide higher on-target fidelity without loss of cleavage efficiency.
Newly engineered eSpCas9 (1.1) enables the efficient targeted gene editing of established CRISPR systems with the benefit of reduced off-target effects. Point mutations (K848A/K1003A/R1060A) in the chromosome-binding motif of SpCas9, as described by Slaymaker, et al., provide higher on-target fidelity without loss of cleavage efficiency.
Ricostituzione
Lyophilized enhanced specificity S. pyogenes eSpCas9-GFP 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.
Altre note
Use our CRISPR Selection Tool to order gRNA
Check out our other MISSION® Cas9 Proteins at SigmaAldrich.com/CRISPRproteins
Check out our other MISSION® Cas9 Proteins at SigmaAldrich.com/CRISPRproteins
Note legali
MISSION is a registered trademark of Merck KGaA, Darmstadt, Germany
Codice della classe di stoccaggio
11 - Combustible Solids
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Articoli
Validate CRISPR gene editing experiments easily with Sigma-Aldrich® T7E1 mismatch detection kit, ensuring successful editing.
Protocolli
Combine guaranteed sgRNAs with our comprehensive range of CRISPR products and tools, including Cas9 and delivery reagents, for efficient genome modification with higher specificity.
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What are the differences between CAS9GFPPRO and ECAS9GFPPR in terms of transfection efficiency and applicability in various cell types?
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