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Avioq Product Line

VioOne HIV Profile
• FDA Approved and CE Mark
• ELISA for confirmation and differentiation of individual antibodies directed to various gene products of HIV-1 and HIV-2
• Human Serum or Plasma
• Proven microelisa technology, microwell solid phase

HTLV-1 Infection

AVIOQ HTLV-I/II Assay
FDA Licensed and CE Marked for:
• Serum and Plasma (Clinical or Donor Testing)
• Serum and Plasma (Deceased Organ and Tissue Donors)
Total incubation time only 2 hours, 30 minutes

Two HIV Particles

AVIOQ HIV-1 Assay
FDA Approved for:
• Serum
• Plasma
• Oral Fluid and Dried Blood Spot

GMP Recombinant Proteins and Synthetic Peptides
• GMP compliant
• Bulk quantities available
• Avioq maintains a FDA (BLA) licensed and ISO 13485 certified manufacturing facility

Avioq, Inc.

104 T.W. Alexander Drive

Research Triangle Park

North Carolina, 27709

United States

Phone: 1.919.314.5535

Email: infor@avioq.com

Products

• Avioq HTLV I/II

 

• Avioq HIV-1

 

• VioOne HIV Profile

 

• GMP Recombinant Proteins

Services

• IVD Assay Development

 

• IVD Contract Manufacturing

 

• Cell Culture Development

 

Contact Us
About Avioq
Support

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