녹아웃(KO) 마우스 | Cyagen Korea

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What Our Customers Say

“Among several commercial services who have claimed to be specialized to generate mouse models with genetic modifications, I recognize that Cyagen is one of the best. We are looking forward to having more cooperation with them.”

Korea Brain Research Institute (KBRI)

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Overexpression 세포주

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None Overexpression Cell Lines Overexpression Cell Lines
Stable cell lines are crucial laboratory tools. Gene overexpression, inducible gene expression, gene knockout, gene knockdown all can be achieved by custom lentiviral-based stable cell line service. With years of gene editing experience, Cyagen has established a comprehensive cell repository which will facilitate your research significantly with our optimized lentiviral platform.
◆ Broad tropism

Lentivirus can target most mammalian cell types including hard-to-transfect cells, primary cells, stem cells and terminally differentiated cells such as neurons.

 

◆ Workflow

  

◆ Why work with Cyagen?
  • Guaranteed: 100% money back guarantee.
  • Substantial experience: Over 13 years of experience with thousands of gene editing projects delivered.
  • Premium services: Experienced scientific team and dedicated project managers provide you with premium services.
  • Customer citations: Over 2,400 publications citing our services and products.

 

1. Custom Overexpression Stable Cell Lines

Our Lentiviral-based overexpression stable cell lines can be used to express large amounts of a protein of interest. After transduced by Lentiviruses, the gene of interest will be integrated into host cell genome and permanently pass to next cell generation. Lentivirus with broad tropism can target most mammalian species and cell types.

We provide our customers with full services from strategy design, vector construction, virus packaging, virus transduction to positive clone selection.

Note: You can choose your selection markers: Antibiotic resistance or GFP for FACS.

 

2. RNA Interference Stable Cell Lines

It allows long-term, inducible RNA interference in human, mouse, and rat cells by using lentiviral-based short hairpin RNA (shRNA). shRNA sequences are encoded in a DNA vector which can be introduced into host cells via lentiviral transduction. shRNA provides a cost-effective, rapid, and high-efficient way for long term down-regulation of target genes.

Compared to synthesized siRNA as well as transient expression of shRNA vector, lentiviral-based shRNA can be transduced and consistently expressed in host cells including primary cells, suspension cell lines, nondividing cells and hard-to-transfect cells.

Note: You can choose your selection markers: Antibiotic resistance or GFP for FACS.

 

◆ Inquiries and quote requests

Request a quote now. Alternatively, you can always email service-apac@cyagen.com to inquire about our services or obtain a quote for your project.

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