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AAV Empty/Full Capsid Ratio Test by AUC

  • We provide gold-standard Analytical Ultracentrifugation (AUC) services, offering unparalleled insights into your AAV preparations. This technique is widely recognized as the gold-standard method for accurately quantifying the empty/full capsid ratio in AAV preparations. As a label-free, high-resolution technique, AUC precisely separates particles based on their sedimentation velocity, enabling clear differentiation between genome-filled capsids, empty capsids, and partial particles. Accurately measuring this empty/full ratio is critical for assessing product potency, mitigating immunogenicity risks, and ensuring overall quality throughout AAV gene therapy development.

AUC
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Key Benefits

  • Gold-Standard Accuracy

  • Direct Quantification

  • High Resolution

Service Details

Our AAV Empty/Full Capsid Ratio Test by AUC service provides precise and reliable quantification of your AAV vector preparations, crucial for demonstrating product quality, potency, and safety.

Feature Detail
Minimum Titer 5.00E+12 vg/mL
Minimum Sample Volume 500µL
Turnaround Time 5 Business Days

Performance

  • Our AAV Empty/Full Capsid Ratio Test by AUC delivers unmatched precision for gene therapy development, manufacturing, and QC. Whether for research, IND-enabling studies, or GMP release testing, our data ensures your AAV product meets the highest safety, efficacy, and regulatory standards.

    Sedimentation coefficient

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