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Animal Models
C57BL/6JCya-Ivdem1/Cya
Ivd is located on chromosome 2 of mice. Nuclease Technology will be used to design sgRNA; Ivd knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
C57BL/6NCya-Cfdem1/Cya
Cfd is located on chromosome 10 of mice. Nuclease Technology will be used to design sgRNA; Cfd knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
C57BL/6JCya-Cfdem1/Cya
Cfd is located on chromosome 10 of mice. Nuclease Technology will be used to design sgRNA; Cfd knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
C57BL/6JCya-Ivlem1/Cya
Ivl is located on chromosome 3 of mice. Nuclease Technology will be used to design sgRNA; Ivl knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
C57BL/6JCya-Bivmem1/Cya
Bivm is located on chromosome 1 of mice. Nuclease Technology will be used to design sgRNA; Bivm knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
C57BL/6JCya-Ivlem1flox/Cya
Ivl is located on chromosome 3 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Ivl conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
C57BL/6JCya-Ivdem1flox/Cya
Ivd is located on chromosome 2 of mice. SgRNA and ssDNA will be designed using Nuclease Technology; Ivd conditional knockout mice will be obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm will be collected for cryopreservation.
C57BL/6JCya-Cfdem1flox/Cya
Cfd is located on chromosome 10 of mice. SgRNA and ssDNA were designed using Nuclease Technology; Cfd conditional knockout mice were obtained by high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
C57BL/6JCya-Scfd1em1/Cya
Scfd1 is located on chromosome 12 of mice. Nuclease Technology was used to design sgRNA; Scfd1 knockout mice were obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
C57BL/6JCya-Siva1em1/Cya
Siva1 is located on chromosome 12 of mice. Nuclease Technology will be used to design sgRNA; Siva1 knockout mice will be obtained by applying high-throughput electroporation of fertilized eggs. After sexual maturity, sperm were collected for cryopreservation.
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Global Antibody Drug Industry Development BlueBook (Frost & Sullivan)
Key Insights
The industry is undergoing a rapid transformation driven by next-generation modalities, globalized markets, and upstream technological innovations.
  • Market Structural Shift: Monoclonal antibodies drive steady growth, but ADCs and bispecifics are rapidly accelerating, reshaping the market with higher-value innovations.
  • Chinese Market Globalization: China is actively expanding globally, evidenced by a surge in high-value cross-border license-out deals.
  • Technology-Driven Efficiency: Advanced discovery engines—exemplified by Cyagen's HUGO-Ab platform and AI algorithms—are streamlining candidate screening, optimizing molecular design, and localizing the upstream supply chain.
  • Oncology-Focused Innovation: R&D pipelines remain heavily concentrated on high-incidence malignancies like non-small cell lung cancer, utilizing complex modalities to combat clinical resistance.
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