Knock-Out

Gene knockout mouse models are beneficial for insight into key genetic mechanisms, accelerating your research. Discover gene functions, understand disease pathogenesis, and advance drug development processes.

  • Conventional knockout
  • Conditional knockout

Knock-Out applications

  • Discover gene functions, explore cellular processes.
  • Gain a deep understanding of disease mechanisms and prevention methods.
  • Simplify the efficacy evaluation in drug discovery.

Using CRISPR gene editing technology

Characteristics of the Cas9 method

  • Short cycle: 4-6 months
  • Efficient, fast, and low-cost
  • Versatility

Using ES cell targeting technology

Characteristics of ES cell targeting technology

  • Long cycle: 7-12 months
  • Mature technology, precise with no off-target effects.
  • Capable of various complex genetic modifications

Conventional Knock-Out

Osteoporosis mice model

  • Osteoprotegerin (OPG) gene polymorphism is associated with bone density
  • The OPG knockout mouse model established using gene knockout technology exhibits clear symptoms of osteoporosis.
  • It provides an ideal animal model for the study of human osteoporosis.

Conditional Knock-Out

Using CRISPR gene editing technology

Using CRISPR gene editing technology

Parkinson's disease mouse model

  • Mutations in the SLC39A14 gene lead to manganese accumulation in the brain and early-onset Parkinson-like pathology.
  • Slc39a14 knockout mice exhibit significant manganese accumulation and behavioral abnormalities.
  • By crossing Slc39a14-flox mice with Alb-Cre mice, liver-specific Slc39a14 knockout mice were obtained, and it was found that the loss of Slc39a14 in the liver was not sufficient to cause manganese accumulation.
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