Professional Gene Editing Services

Comprehensive gene editing services, from gene knockout to high-throughput screening, empowering your research innovation

Gene Knockout Service
Precise gene knockout using CRISPR/Cas9 technology

Our gene knockout service uses state-of-the-art CRISPR/Cas9 technology to achieve efficient and precise gene knockout in various cell lines. From sgRNA design to monoclonal cell line establishment, we provide comprehensive technical support.

Key Features:

  • Efficient sgRNA design and validation
  • Multiple cell line support
  • Monoclonal screening and identification
  • Complete sequencing validation report
Targeted Knock-in Service
Precise gene targeted insertion technology

Through HDR (Homology-Directed Repair) or NHEJ (Non-Homologous End Joining) mechanisms, we can achieve precise insertion of target genes. We support various knock-in strategies, including Safe Harbor locus knock-in and tag protein fusion.

Key Features:

  • Safe Harbor locus knock-in
  • Tag protein fusion expression
  • Reporter gene knock-in
  • Conditional knock-in system
High-Throughput Gene Editing
Automated large-scale gene editing screening

Our high-throughput gene editing platform combines automated liquid handling systems with advanced sequencing technology, enabling functional screening of thousands of genes simultaneously, greatly accelerating research progress.

Key Features:

  • Genome-wide CRISPR screening
  • Candidate gene function validation
  • Drug target screening
  • Automated data analysis
Gene Knockdown Service
Controllable gene expression suppression

We provide multiple gene knockdown strategies, including CRISPRi, shRNA, and siRNA methods. Reversible, dose-dependent gene expression suppression can be achieved, suitable for gene function research and drug target validation.

Key Features:

  • CRISPRi technology
  • shRNA/siRNA design
  • Inducible knockdown system
  • Expression level validation
Stable Cell Line Construction
High-quality stable expression cell lines

Using advanced viral vector systems to construct high-expression, high-stability cell lines. We support both constitutive and inducible expression systems to meet different research needs.

Key Features:

  • Lentiviral/retroviral system
  • Inducible expression system
  • Multi-gene co-expression
  • Stability validation
Customized Service
Tailored to your specific needs

Our expert team will provide personalized technical solutions based on your specific research needs. From project design to implementation, we provide professional technical support and consulting services throughout the process.

Key Features:

  • Project design
  • Technical consulting support
  • Experimental optimization
  • Data analysis and interpretation

Our Advantages

Choose ELEM Biotech, choose professionalism and quality

Advanced Technology

Using the latest CRISPR technology and automation platforms

Quality Assurance

Strict quality control system ensuring reliable experimental results

Fast Delivery

Optimized workflow to shorten project timelines

Professional Team

Experienced researchers providing technical support

Service Workflow

Simple and efficient collaboration process to ensure smooth project execution

01

Requirements Discussion

Understand your research goals and technical needs

02

Solution Design

Develop detailed experimental plan and quotation

03

Project Implementation

Professional team executes experiments with regular updates

04

Results Delivery

Provide complete experimental data and analysis report

Start Your Project

Contact us for professional technical consultation and customized service solutions

ELEM Biotech - 粒曼生物

Professional high-throughput gene editing solutions provider, dedicated to advancing drug discovery and fundamental research innovation.

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