The Diagnostic Reference panels consist of individual serum or plasma samples.
They are patient consented, clinically characterized, and physician documented.

• Delinked
• Diagnostically Characterized
• IRB Approved

CURRENTLY AVAILABLE REFERENCE PANELS:

Clinical Validation Panels

Clinical Normal Panel
CATALOG #CN-6710 (25 Specimens 1.0mL)

Flu Vaccine Panel
CATALOG #6230 (26 Specimens 1.0mL)

Post Menopausal Panel
CATALOG #PM6310 (24 Specimens 1.0mL)

Diagnostic Reference Panels

Autoimmune Disease Panel
CATALOG # 6405 (10 Specimens 0.5mL)

PSA Sensitivity Panel
CATALOG # PR-6115 (15 Specimens 1.0mL)

HAMA Panel
CATALOG # HM-6111 (15 Specimens 1.0mL)

Misc Panels

Syphilis Mixed Titer Panel
CATALOG # K-ZMC002 (15 Specimens 1.0mL)

ToRCH Mixed Titer Panel
CATALOG #K-ZMC004 (24 Specimens 0.5mL)

Hepatitis E Positive Titer Panel
CATALOG # K-ZMC003 (24 Specimens 0.5mL)

Global HIV Surveillance Panel
CATALOG # KGSP101 (24 Specimens 0.25mL)

Mixed Titer Bacteria Panel
CATALOG #0820000

CUSTOM OEM PANELS:

Any specific panel matrix can be developed to complement your custom application. Specific Areas Include:

New Product Development
Regulatory Submissions
Kit “lot” Release & other QC Applications
Clinical Trials
Training
Equipment Validation & Familiarization

You can use this form to design and order
custom panels.