Genome Engineering
- Cas9 Activity Assays
- Cas9 Protein with Nuclear Localization Signal
- Cas9 Quantitation
- CRISPR Cas9 AAVS1 Safe Harbor Knockin System
- CRISPR Cas9 AAVS1 Safe Harbor Targeting System
- CRISPR Cas9 Expression Constructs
- CRISPR Cas9 Guide RNA Custom Constructs
- CRISPR Cas9 Lentiviral Guide RNA Cloning Vectors and Control Constructs
- CRISPR Cas9 Lentiviral Guide RNA Libraries with expressed barcodes for RNA-Seq / Perturb-Seq
- CRISPR Cas9 Lentiviral Guide RNA Premade Libraries
- CRISPR Cas9 Lentiviral sgRNA Premade Particles
- CRISPR Cas9 Multiplex Guide RNA Cloning Kits
- CRISPR Cas9 pCAS-Guide Genome Engineering System: Gene-specific Ready-to-Go Knockout Kits
- CRISPR Cas9 pCAS-Guide Genome Engineering System: Vector-based
- CRISPR Cas9 Retroviral Cloning Vectors
- CRISPR Cas9 ROSA26 Safe Harbor Targeting System
- CRISPR Cas9 SmartNuclease Genome Engineering System: AAV vector-based for in vivo applications
- CRISPR Cas9 SmartNuclease Genome Engineering System: Lentiviral Vector-based
- CRISPR Cas9 SmartNuclease Genome Engineering System: RNA-based for in vivo applications
- CRISPR Cas9 SmartNuclease Genome Engineering System: Vector-based
- CRISPR Human sgRNA Libraries for Gene Knockout
- CRISPR/CAS9 Antibodies
- CRISPR/CAS9 RT-PCR Primers
- CRISPRa Lentiviral Guide RNA Premade Libraries
- CRISPRi Lentiviral Guide RNA Premade Libraries
- crRNA Oligo Template Synthesis
- Custom Clonal Gene Knockout/Editing Cell Line Engineering
- Custom CRISPR Cell Line Engineering
- Custom Knockout Cell Line Engineering
- Gene Editing Quantitation
- Homologous Recombination Targeting Vectors
- Indel Detection
- Recombinant CAS9 Nucleases and Nickases
- Recombinant Cpf1 Nucleases
- sgRNA expressing Lentivirus Controls for Cas9 Cell Lines
- TALE-Nuclease AAVS1 Targeting
- Transcriptional Activation of endogenous genes by CRISPR/Cas9 SAM
- Transcriptional Activation of endogenous genes by dCas9-VPH
- Transcriptional Repression of endogenous genes by dCas9-KRAB
Powerful Tools for Engineering Genomes
Genome editing technologies using engineered, site-specific nucleases including designer Transcription Activator-Like Effector Nucleases (TALENs) and Cas9/CRISPR-mediated multiplex Genome editing abilities have revolutionized the field of engineering target genomes.
These designed nucleases, when used in combination with Homologous Recombination (HR) targeting vectors, now enable gene knock-outs, knock-ins and even single base Genome editing on demand.