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GeneArt® CRISPR Nuclease Vector with CD4 Enrichment Kit

日期: 2015-06-01
浏览次数: 753

货号: A21175

 

规格

 

Promoter: CMV, U6
Reporter: CD4
Key Function: Gene Editing, Stable Cell Line Development, Genome Engineering, Episomal Expression
Product Size: 10 reactions
Cloning Method: Restriction Enzyme ⁄ MCS
Delivery Method: Transfection
Protein Tag or Fusion: CD4 fusion

 

内容及储存

 

Contains:
• CRISPR CD4 Nuclease Vector, linearized
• 10X Oligonucleotide Annealing Buffer
• DNase/RNase-free Water
• 5X Ligation Buffer
• T4 DNA Ligase
• U6 Forward Sequencing Primer
• Control Double-stranded Oligonucleotide

Store in freezer (-5 to -30°C).

 

描述

 

The GeneArt® CRISPR Nuclease Vector with CD4 Enrichment Kit is a vector system for expression of the functional components needed for CRISPR/Cas9 genome editing in mammalian cells with a CD4 reporter. The CD4 reporter enables bead-based enrichment, an option for magnetic bead-based sorting/enrichment of Cas9 & CRISPR expressing cells using Dynabeads® CD4 magnetic beads. Transfection efficiency can also be tracked using anti-CD4 fluorescent antibodies. The linearized GeneArt® CRISPR nuclease vectors provide a rapid and efficient way to clone double-stranded oligonucleotides encoding a crRNA representing a desired target into an expression cassette that allows sequence-specific targeting of the Cas9 nuclease.

The GeneArt® CRISPR Nuclease Vector system offers:

• Easy–to-design genome engineering system
• Affordable, ready-to-use cloning vectors
• Enrichment for hard to transfect or difficult to modify cell lines

All-in-one Vector System for CRISPR-based Genome Editing
The GeneArt® CRISPR Nuclease Vector kit offers a simple, ready-to-use, all-in-one expression vector system consisting of both a Cas9 nuclease expression cassette and a guide RNA (gRNA) cloning cassette for rapid and efficient cloning of DNA that encodes target-specific CRISPR RNA (crRNA). This system allows you to edit and engineer a genomic locus of choice in a sequence-specific manner from a single plasmid. After relevant targets have been identified with fast and easy-to-use GeneArt® CRISPR vectors, the biologically relevant mutations can be precisely created with GeneArt® Precision TALs, with high specificity and low off-target effects.

 

 

 

 

 

 

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