Reveal® Q+ for Fumonisin

Item No.  8885

  • Quantitative lateral flow format
  • For use with portable reader with data management software
  • Rapid and accurate quantitative testing
This item has shipping restrictions.
$336.81 each
In stock
Out of stock
Expect availability in 2-4 weeks
Minimum quantity required: 1
This item must be ordered in multiples of one case. Quantity per case: 1
Reveal® Q+ for Fumonisin is a single-step lateral flow immunochromatographic assay based on a competitive immunoassay format intended for the quantitative testing of fumonisin in grain and grain products.
Brand Reveal®
Analyte Fumonisin
Platform Lateral Flow
Result Type Quantitative
Approvals FGIS: 2018-116
Limit of Detection 0.3 ppm
Testing Time 6.00
Quantity per Package 25 tests
Package Dimensions 8.30 in x 5.20 in x 2.40 in
Package Weight 0.44
  1. 25 Reveal Q+ for Fumonisin test strips
  2. 25 red sample dilution cups
  3. 25 clear sample cups
  4. 1 bottles of sample diluent
  5. Instructions for use
  1. 65% ethanol solution (Neogen® item 8073, 8074)
  2. Sample collection cups with lids (Neogen item 9428)
  3. Agri-Grind grinder or equivalent (Neogen item 9401, 9453)
  4. Scale capable of weighing 5–50 g ± 0.1 g (Neogen item 9427)
  5. Timer (Neogen item 9426)
  6. Reveal sample cup rack (Neogen item 9475)
  7. AccuScan reader: AccuScan III (Neogen item 9590), AccuScan Pro (Neogen item 9565), or AccuScan Gold (Neogen item 9595)
  8. Dispensing pump or graduated cylinder (Neogen item 9448, 9447)
  9. Filter syringe or Whatman no.1 filter (Neogen item 9420, 9430)
  10. Sample collection tubes with caps (Neogen item 9421, 9421B)
  11. Pipettor, 100 µL (Neogen item 9272, 9278)
  12. Pipette tips, 100 µL (Neogen item 9407, 9410, 9417)
  13. Pipettor, 200 µL (Neogen item 9488)
  14. Pipette tips, 200–1000 µL (Neogen item 9464, 9487)


To access the Certificate of Analysis (COA), please use our COA Search.


Assay Principle

Reveal Q+ for Fumonisin is a single-step lateral flow immunochromatographic assay based on a competitive immunoassay format. The extract is wicked through a reagent zone, which contains antibodies specific for fumonisin conjugated to colloidal gold particles. If fumonisin is present, it will be captured by the particle-antibody complex. The fumonisin-antibody-particle complex then is wicked onto a membrane, which contains a zone of fumonisin conjugated to a protein carrier. This zone captures any uncomplexed fumonisin antibody, allowing the particles to concentrate and form a visible line. As the level of fumonisin in a sample increases, free fumonisin will form a complex with the antibody-gold particles. This allows less antibody-gold to be captured in the test zone. Therefore, as the concentration of fumonisin in the sample increases, the test line density decreases. Algorithms programmed into the AccuScan® readers convert these line densities into a quantitative result displayed in parts per million (ppm). The membrane also contains a control zone where an immune complex present in the reagent zone is captured by an antibody, forming a visible line. The control line always will form regardless of the presence of fumonisin, ensuring the strip is functioning properly.


Our customers’ success is our shared success. Our experts are ready to train you and your team on our solutions, so you can rest easy knowing procedures are performed properly and yield accurate results. In addition, we provide certificates upon completion of training to provide you with the documentation needed for audit traceability.



Our experts are here to help. If you need information beyond what is provided in Validation Reports under the Documents tab, please contact us and we will be happy to assist you. Learn more