Description
Premium T7 Endonuclease I for CRISPR/Cas9 Validation and Mutation Detection
Transform your gene editing experiments with riboEDIT™ T7 Endonuclease I, the gold standard enzyme for CRISPR validation and mutation detection. Our high-fidelity enzyme delivers premium accuracy in identifying CRISPR-induced mutations, DNA mismatches, and structural variations, making it an indispensable tool for modern genome editing workflows.
Advanced Features for CRISPR Validation
Our premium mismatch detection enzyme T7 Endonuclease I brings superior specificity with sensitivity to your CRISPR validation process:
- Industry standard specificity for detecting and cleaving mismatched DNA heteroduplexes with precision down to single-base resolution
- Enhanced sensitivity capable of identifying the smallest genetic variations, including point mutations, insertions, and deletions
- Optimized enzymatic activity through recombinant production ensures batch-to-batch consistency
- Rigorous validation through extensive testing across diverse CRISPR applications and workflows
- Convenient ready-to-use format with our proprietary reaction buffer for maximum efficiency
Comprehensive Applications in Genome Engineering
Elevate your research with a versatile tool perfect for:
- Rapid assessment of CRISPR/Cas9 editing efficiency
- High-throughput mutation detection assays
- Precise SNP analysis and verification
- Advanced heteroduplex analysis
- Comprehensive DNA mismatch screening
- Quality control in gene editing protocols
- Validation of genetic modifications
- Off-target effect analysis
Why Choose riboEDIT™ T7 Endonuclease I?
Developed specifically for demanding CRISPR applications, our riboEDIT™ enzyme delivers reliable results for both routine validation and challenging gene editing projects. The optimized formulation ensures consistent performance while minimizing background noise, making it the preferred choice for researchers who demand accuracy in their genome editing experiments.
Our premium riboEDIT™ T7 Endonuclease I is backed by extensive validation data and comes with comprehensive technical support to ensure success in your gene editing workflows.
For research use only. Not for use in diagnostic procedures
