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Cambridge Nutritional Sciences Ltd
Eden Research Park
Henry Crabb Road
Littleport, Cambridgeshire
United Kingdom, CB6 1SE

TEL: 44 (0) 1353 863279
FAX: 44 (0) 1353 863330
Email: info@camnutri.com
Web: www.camnutri.com
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Testimonial

"I'd have put money on my symptoms being food-related, but none of the medics would entertain that idea until I took the Food Detective test", John Morris, West London. The test confirmed that John did indeed react to dairy, wheat and a whole host of other common ingredients and foods. Milk was the main culprit, but yeast, egg white, cola nut, wheat, pineapple and barley were also on his 'to-ban' list. John said "People who suspect an intolerance to some foods should take a test like Food Detective; carefully read ingredients lists on pre-packaged foods....and get a good cookbook"!
John Morris, West London
Retired Businessman

Foodprint® Indicator - Technical Literature

The Foodprint® Indicator Test utilizes basically the same technology as the Foodprint® 40, 60, 120 and 200+. The Genarrayt® Food IgG test is a rapid colorimetric microarray-based ELISA for the measurement of IgG antibodies for up to 221 foods in whole blood, human serum or plasma. Genarrayt® Microarray Food IgG technology has been developed by our sister company Genesis Diagnostics Ltd. For further information visit www.elisa.co.uk

Explanation of the Test
Many people exhibit chronic food sensitivity reactions to specific food antigens.  Unlike the immediate effects of IgE-mediated allergy, IgG-mediated food sensitivity reactions may take several days to appear. Controlled removal of the problem foods from the patient’s diet will, in many cases, rapidly improve the patient’s condition. General lethargy, weight gain, dermatitis, arthritis and tiredness are associated with food intolerances.  Irritable bowel syndrome may also be linked to food sensitivity.

Principle of the test

Up to 221 foods are microarrayed onto each of 16 nitrocellulose pads on a glass microscope slide.  Non-specific binding sites are blocked with blocking buffer prior to incubation with diluted patient whole blood, serum or plasma. After washing away unbound serum components, anti-human IgG conjugated to horseradish peroxidase is added to the pads, and this binds to food extract-bound antibodies in the second incubation. Unbound conjugate is removed by washing, and a solution containing 3,3’,5,5’-tetramethylbenzidine (TMB) and enzyme substrate is added to trace specific antibody binding. After washing with distilled water, the slides are dried by centrifugation prior to scanning.The optical densities of the standards, positive and negative controls and samples are measured using a high resolution flat bed scanner with associated software.Optical density is directly proportional to antibody activity in the sample.