Knock-in iPS Cell Generation Service Details

Service Advantages:

  • Optimized CRISPR protocols for high success rate
  • Footprint-free, feeder-free transfection and iPSC culture protocols
  • Isogenic control lines for reliable experiments
  • Knock-in a variety of genes for different applications
    • Locus-specific small/ large fragment gene insertions
    • Safe harbor locus knock-in
    • Reporter gene knock-in/ gene tagging
    • Gene overexpression (Ex. Antibody/ antigen expression)
    • Promoter modifications
    • Gene replacement; gene therapy
    • Gene fusion/ translocation

Standard Packaging:

Standard Deliverables:

  • Two (2) clones that are homozygous for the targeted insertion, with two (2) vials of each clone at 1 x 10^6 cells/vial.
  • Project Milestones Reports, as well as a Final Report containing details of targeting design, experimental, and genotyping results.

Standard Workflow and Timeline:

Workflow includes:

  • Cell line evaluation
  • gRNA design, CRISPR vector, and donor DNA construction, and reagent validation
  • Transfection of targeting vectors and optimization
  • Screening for single cell clones and clone confirmation
  • Cell expansion and cryopreservation

Timeline: 3-4 months

Required Starting Material & Information

Applications:

  • Physiologically relevant disease models for hard-to-model diseases (Ex. ALS, muscular dystrophy, Parkinson’s disease, Alzheimer’s)
  • Differentiate to study mutations in different tissue lineages with an isogenic panel of cell line models
  • Ideal for target drug discovery, drug and toxicity screening

Also available, downstream iPSC differentiation and characterization services.

Reviews

There are no reviews yet.

Be the first to review “CRISPR (Cas9) Knock-in iPSC Service”

Your email address will not be published. Required fields are marked *