Art. No.: RBRDP07 / RBRP07
The procedure is based on monoclonal antibody technology, which makes the test highly specific, sensitive, rapid and simple to perform.
The columns contain a gel suspension of monoclonal antibody specific to the toxins of interest. Following extraction of the toxins the sample extract is filtered, diluted and passed slowly through the immunoaffinity column. Any toxins which are present in the sample are retained by the antibody within the gel suspension. The column is washed to remove unbound material and the toxins are then released from the column following elution with solvent. The eluate is collected prior to analysis by HPLC or LC-MS/MS. Aflatoxins are required to be derivatised when anal HPLC or LC-MS/MS. Aflatoxins are required to be derivatised when analysed by HPLC.
Premium quality and performance:
- Exceeds Official Method criteria
- Demonstrated performance in collaborative trials
- Numerous publications referencing the product and demonstrating superior performance
- The preferred supplier of immunoaffinity columns in proficiency testing rounds
- High antibody loading ensuring excellent recoveries
- Optimised methods to ensure ease of analysis
- Ability to work with highly contaminated samples
- Manufactured with bespoke automated systems ensuring product consistency and providing unique batch number etching
- Dedicated technical support available from our expert team
- Global mycotoxin test kit supplier for over 35 years
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|Art. No||RBRDP07 / RBRP07|
|Test format||10 columns (1 ml format) (RBRDP07)|
50 columns (1 ml format) (RBRP07)
500 columns ( 1ml format) (RBRP07/500)
|Sample preparation||A representative sample should be obtained by following an officially recognised sampling procedure. Sample is extracted using solvent (Extraction solvent can vary depending on the commodity analysed) filtered and diluted ready for applying to the immunoaffinity column.|
|LOD (Detection Limit)||Information provided is typical LOD obtained by R-Biopharm. Please note that this is dependant on method, LC conditions and equipment used.|
B1 0.031 ng/ml
B2 0.016 ng/ml
G1 0.031 ng/ml
G2 0.004 ng/ml
Aflatoxin B1, Aflatoxin B2, Aflatoxin G1 and Aflatoxin G2. May also cross react with other metabolites.
|Available application notes|
Methods are available for all matrices covered by legislation as well as additional commodities. Please contact your local R-Biopharm distributor for further information.
|Evaluation||HPLC or LC-MS/MS.|
|Approvals||The product has been used in numerous CEN and AOAC collaborative trials and meets all Official Method recovery and capacity specifications.|