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ECAS9GFPPR

Sigma-Aldrich

eSpCas9-GFP Protein

from Streptococcus pyogenes with mutations conferring enhanced specificity, fused with enhanced GFP, recombinant, expressed in E. coli, 3X NLS

Sinônimo(s):

eSpCas9-EGFP, eSpCas9-GFP

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50 μG
R$ 2.355,00
250 μG
R$ 4.730,00

R$ 2.355,00


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Selecione um tamanho

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50 μG
R$ 2.355,00
250 μG
R$ 4.730,00

About This Item

Código UNSPSC:
12352202
NACRES:
NA.51

R$ 2.355,00


Check Cart for Availability

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recombinante

expressed in E. coli

Ensaio

≥90% (SDS-PAGE)

Formulário

lyophilized powder

embalagem

pkg of 1 kit (3 components)

gene repórter

GFP

Condições de expedição

wet ice

temperatura de armazenamento

−20°C

Descrição geral

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.

Aplicação

  • Functional Genomics
  • Target Validation
  • Genome Editing
  • Fluorescence Microscopy
  • Flow Cytometry

Características e benefícios

  • Enhanced specificity compared to wild type Cas9
  • Highly active
  • Ready-to-inject/transfect

Embalagem

pkg of 50 μg ( ≥260 pmol )
pkg of 250 μg ( ≥1300 pmol)

Componentes

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

Princípio

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.

Reconstituição

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.

Outras notas

Use our CRISPR Selection Tool to order gRNA

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

Informações legais

MISSION is a registered trademark of Merck KGaA, Darmstadt, Germany

Código de classe de armazenamento

11 - Combustible Solids


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Questions

  1. What are the differences between CAS9GFPPRO and ECAS9GFPPR in terms of transfection efficiency and applicability in various cell types?

    1 answer
    1. 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.

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