Express Gene-to-AAV Production Service in Southeast Asia

Express Gene-to-AAV Production Service in Southeast Asia

Tired of long turnaround times and unreliable AAV production?

Our Express Gene-to-AAV service offers a streamlined and efficient solution to accelerate your research. By combining expert design, rapid production, and rigorous quality control, we deliver high-quality AAV vectors in just 4 weeks.

Our Express Gene-to-AAV Service Includes:

Serotype60+ serotypesVector typeOver-expression, CRISPR, shRNA, miRNA, etc.
AAV typessAAV, scAAVPromoterCMV, CAG, EFS, hSyn, U6, H1 etc. or custom promoter
Packaging plasmidEnhanced yield with PackGene-provided RC and helper plasmidGene of InterestCustom Gene, or pre-synthesized gene elements (Reporter, Gene editing, etc.)
  1. Gene Synthesis and Cloning:
    • Expert Design: Our experienced team designs optimal gene constructs.
    • Efficient Cloning: We utilize advanced cloning techniques to ensure rapid and accurate gene insertion.
  2. AAV Vector Production:
    • High-Titer AAVs: We produce high-titer AAVs with a range of serotypes to maximize transduction efficiency.
    • Rigorous Quality Control: Our stringent quality control measures ensure purity, potency, and safety.
  3. Comprehensive Quality Control:
    • Purity and Potency: We perform comprehensive tests to assess the purity and titer of your AAV vectors.
    • Safety Testing: We conduct rigorous safety testing to ensure compliance with regulatory standards.

What do you get from our Express Gene-to-AAV Service?

  1. AAV Vector: High-quality AAV vector, ready for your research experiments.
  2. Detailed Quality Control Report: Comprehensive documentation of vector quality and performance.
  3. Plasmid Map and Sequence: Detailed information about the plasmid construct used for AAV production.
  4. Customizable Reporting: Tailored reports to meet your specific needs.

Why Choose PackGene?

  • Rapid Turnaround Time: Experience accelerated timelines with our efficient production process.
  • Customizable Solutions: Tailor your AAV vectors to your specific research needs, including serotype, promoter, and transgene selection.
  • Unmatched Quality: Benefit from our commitment to quality, ensuring consistent and reliable results.
  • Expert Technical Support: Experienced team provides guidance and support throughout the entire process.
  • Competitive Pricing: Cost-effective solutions help you maximize your budget.

Case Study

  • Case 1
  • Case 2
  • Case 3
  • Case 4
Screenshot of a mother’s testimonial in Chinese dated September 19, 2024, describing her two children’s improvements after 13 days of gene therapy and anti-epileptic medication. She shares that one child no longer has seizures for 11 days, the other can now walk, eat, and ride a bicycle, and her child has started practicing climbing stairs again.
  • Spinal muscular atrophy with myoclonic epilepsy (SMA-PME, ASAH1 gene defect)
  • Single dose, intrathecal and intracerebroventricular injection.
Screenshot of a research article titled “AAV1-hOTOF gene therapy for autosomal recessive deafness 9: a single-arm trial,” reporting that in six children with OTOF-related hereditary deafness, five showed significant improvement in hearing and speech after AAV1-hOTOF treatment, demonstrating good safety and efficacy.
  • OTOF biallelic mutations cause severe hearing impairment or complete hearing loss.
  • Single dose, cochlear injection.
Screenshot of a Chinese news article reporting that GenAns Biotech (Jienda Jiuzhou) achieved a breakthrough with its GA001 gene therapy. A patient with total blindness regained light perception under the guidance of Professor Zhang Xuxiang (张旭乡), showing early evidence of safety and efficacy in treating retinal degenerative diseases.
  • Advanced blindness caused by retinitis pigmentosa.
  • Single dose, intraocular intravitreal injection.
Screenshot of a Chinese news article reporting that SineuGene Therapeutics announced positive clinical progress for its SNUG01 gene therapy in amyotrophic lateral sclerosis (ALS). The study, led by Professor Fan Dongsheng at Peking University Third Hospital, showed no serious adverse reactions and early signs of safety and therapeutic potential.
  • Amyotrophic lateral sclerosis (ALS).
  • Single dose, intrathecal injection.

Your Success, Our Priority

By choosing PackGene, you’re investing in a partnership dedicated to your research success. Our team is committed to providing exceptional service and delivering high-quality AAV vectors.

Contact us today to discuss your specific research needs and learn how our Express Gene-to-AAV service can accelerate your scientific discoveries.

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