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Custom Mammalian Gene Editing

Biology

Custom Mammalian Gene Editing

DCB offers a full CRISPR (Clustered Regulatory Interspaced Short Palindromic Repeats) based gene editing service, to produce a genetically modified cell using any mammalian cell line and targeting any gene.

CRISPR/Cas9 systems is a newly developed yet the most popular method for genome editing. Our scientists are experts at performing gene editing with CRISPR, from designing specific gRNA constructs to transfection and single clone generation of a wide range of cells.

Why DC Biosciences?

  • Expert guidance through project design and completion
  • Many years of experience with a variety of cell lines
  • Cost-effective and competitive pricing
  • Continual interaction at all stages of the process
We Offer

  • Multiple Modification Options: permanent knock-out, conditional knock-out, point mutation, insertion
  • Complete Service: we design and clone the gRNA and HR donor plasmid as well as generate a stable cell line
  • Timeline: 2-4 months depending on project requirements
  • Required Materials: cell line (2 vials) and indication of culture media and supplements
  • Deliverables: 5 vials of mutant cells
Interested in any of our services?
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