Description
CRISPR Libraries Construction
CRISPR technology has become one of the most effective methods for gene/genome editing. CRISPR libraries/sgRNA libraries can simultaneously edit multiple genes in a signal pathway or an entire genome. This makes it a powerful research tool in CRISPR screening. Through functional screening and enrichment, PCR amplification, and deep sequencing analysis, the functional gene can be identified. With the same techniques, the related signal pathway and molecular mechanism can also be recognized. This technology has been widely used in physiology mechanism, cancer diagnosis, drug discovery, etc.
Synbio Technologies has more than ten years of high standard CRISPR gRNA library experience. We provide customers around the world with precise, efficient, and customized solutions. Some of these include sgRNA design, oligo pool synthesis, CRISPR library/sgRNA library construction, NGS validation, and high-content screening.
Highlights
- Precision Editing with Minimal Off-target Effect
- One Stop Solution, Starting from Genome Wide sgRNA Design to Library Construction
- Construction of Any Type of Library for Any Species
- Fast Delivery of Transfection Grade Plasmids
Service Details
| Service Specifications | Service Steps | Turnaround Time |
|---|---|---|
| sgRNA Design | sgRNA sequences are designed for specific genes 3-6 sgRNAs for each target gene | 1-2 weeks |
| Oligo Pool Synthesis | All designed sgRNAs and negative controls will be synthesized simultaneously | 3-4 weeks |
| sgRNA Library Construction | Cloning sgRNAs pool onto the target vector | 2-3 weeks |
| Plasmid Purification | Transfection-grade plasmid preparation to meet the shipping need | 1 week |
| Library Quality NGS Verification(Optional) | 1.100x greater library coverage 2.>70% cloning accuracy rate 3.>99% library accuracy rate by NGS verification 4.<10 library uniformity index | 2-3 weeks |
| Total | 9-13 weeks | |
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