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ZeptoMetrix Corporation SeroDetect™ QC Validation Panels

For monitoring assay performance across wide range of reactivity levels

Specifications

Biosafety Level 2
Format Solution
For Use With (Application) In vitro assay procedures for the determination of Antibodies to Hepatitis C Antigen (Anti-HCV)
Media Type Vial
Shelf Life 60 Days
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Alert:

Product capable of transmitting infectious agents.


Products 1
Catalog Number Mfr. No. Product Type Quantity Price Quantity & Availability  
Catalog Number Mfr. No. Product Type Quantity Price Quantity & Availability  
22-157-299
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ZeptoMetrix Corporation
KZMC012
SeroDetect HIV Ag/Ab Combo Panel 5 x 1.25mL This item has been discontinued by the manufacturer and is no longer available. Please call customer service for assistance: 1-800-766-7000.
Due to product restrictions, please to purchase or view availability for this product.
N/A
Description

Description

  • Prepared from proteins derived from human sources, and non human components (antimicrobial agents and stabilizers)
  • Processed to eliminate contaminants
  • Needs evaluation of members as per instructions

CMV IgG Range Validation Panel

  • Three vials SeroDetect CMV IgG Negative (1.5mL each)
  • Seven vials SeroDetect CMV IgG Positive (1.5mL each)
CMV IgG Panel
  • One vial SeroDetect CMV IgG Negative (1.5mL each)
  • Four vials SeroDetect CMV IgG Positive (1.5mL each)
Mixed Titer Panel I
  • One vial SeroDetect HIV positive material (1.25mL)
  • One vial SeroDetect HBsAg positive material (1.25mL)
  • One vial SeroDetect HBc Total positive material (1.25mL)
  • One vial SeroDetect HBc IgM positive material (1.25mL)
  • One vial SeroDetect Negative material (1.25mL)
HIV Ag/Ab Combo Panel
  • One vial SeroDetect HIV, non-reactive for antibodies and antigens to HIV (1.25mL)
  • Four vials SeroDetect HIV, containing antibodies and antigens to HIV (1.25 each)

Not substitute for mandatory positive and negative control reagents provided with licensed test kits.

For training, lot-to-lot comparison of reagent test kits and to evaluate and compare intra laboratory and inter laboratory performances

Specifications

Specifications

2
In vitro assay procedures for the determination of Antibodies to Hepatitis C Antigen (Anti-HCV)
60 Days
Solution
Vial
2° to 8°C
SDS
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