Home / Clinical Laboratory / Test Kits / Test Kit / Test Kit ImmunoDOT™ Mono-M ELISA Epstein-Barr Virus / Cytomegalovirus / Toxoplasma Serum Sample 25 Tests800-6025
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Test Kit ImmunoDOT™ Mono-M ELISA Epstein-Barr Virus / Cytomegalovirus / Toxoplasma Serum Sample 25 Tests800-6025

Test-Kit-ImmunoDOT™-Mono-M-ELISA-Epstein-Barr-Virus--Cytomegalovirus--Toxoplasma-Serum-Sample-25-Tests800-6025

SKU #

#795469

MPN #

800-6025

Brand

Genbio

Stock

In Stock

Quantity

100

Features

TEST KIT, LAB MONO M IMMUNODOT(25/KT)

$647.58 USD

Product Specifications Product Usage Additional Information
Print
Attribute Name Attribute Value
McKesson # 795469
Manufacturer # 800-6025
Brand ImmunoDOT™ Mono-M
Manufacturer Genbio
Application Test Kit
CLIA Classification CLIA Moderate Complexity
Contents Assay Strips, Diluent (#1), Enhancer (#2), Conjugate (#3), Developer (#4), Reaction Vessels
Number of Tests 25 Tests
Reading Type Visual Read
Sample Type Serum Sample
Storage Requirements Requires Refrigeration
Test Format Dipstick Format
Test Method Enzyme-linked Immunoabsorbent Assay
Test Name Epstein-Barr Virus / Cytomegalovirus / Toxoplasma
Test Type ELISA
Time To Results 135 to 175 Minute Results
UNSPSC Code 41116126
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  • ImmunoDOT is an easy-to-use, visually interpreted, rapid-test format, dipstick ELISA that allows individual patients to be tested for multiple parameters simultaneously
  • ImmunoDOT is a sophisticated test format which is a multiparameter, nitrocellulose ELISA with sensitivities and specificities similar to reference method western blots
  • The Mono-M Test is a qualitative enzyme immunoassay (EIA) that detects IgM antibodies to Paul-Bunnell heterophil, Epstein-Barr virus capsid antigen (EBV-VCA), and cytomegalovirus (CMV)
  • When used in conjunction with Mono-G Test, it is an aid in the serodiagnosis of infectious (EBV) mononucleosis and presumptive serodiagnosis of CMV mononucleosis-like syndrome
  • This assay has not been FDA cleared or approved for the screening of blood or plasma donors
  • Performance with this device has not been established for either prenatal screening or newborn testing
  • Performance of this assay has not been established in a non-clinical laboratory environment (e.g., point of care testing)
  • The assay uses an enzyme-linked immunoassay (EIA) dot technique for the detection of antibodies