Detection method for on-site fast detection protein nitrogen
A detection method, protein nitrogen technology, which is applied in the field of food analysis, can solve the problems of high detection cost, high price, unsuitable detection, etc., and achieve the effect of simple, convenient and fast operation and low use cost
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Embodiment 1
[0024] A detection method for rapidly detecting protein nitrogen on the spot, which is made by using the result obtained after the color reaction of protein standard substance with protein nitrogen content of 10-40% and iTAG reagent or Coomassie brilliant blue staining reagent or Folin-phenol reagent Standard color comparison card, take 0.2 g of milk powder of the sample to be tested, dilute to 10 ml with distilled water, take 2 g of the solution and add it to a 50 ml beaker, then add iTAG reagent or Coomassie brilliant blue staining reagent or Folin-phenol reagent 2 After mixing evenly, the color develops, and the content of protein nitrogen in the sample is read by comparing the card reader with the standard color card.
Embodiment 2
[0026] A detection method for on-site rapid detection of protein nitrogen, using a standard colorimetric card made from the result of the color reaction between a protein standard with a protein nitrogen content of 10-40% and iTAG reagent, and setting it on a handheld In the colorimeter, take 2 grams of milk as the sample to be tested, add 2 grams of distilled water to dilute, then take 2 grams of sample and add it to the sample hole of the hand-held colorimeter, then add 2 grams of iTAG reagent, mix well and develop color, and The content of protein nitrogen in the sample is read by comparison with the standard color card.
Embodiment 3
[0028] A colorimetric test paper, a standard colorimetric card made from the results obtained after the color reaction of a protein standard with a protein nitrogen content of 10-40% and iTAG reagent or Coomassie brilliant blue staining reagent or Folin-phenol reagent It consists of two parts, the test area coated with iTAG reagent or Coomassie brilliant blue staining reagent or Folin-phenol reagent.
[0029] The following samples are each taken in an appropriate amount (0.2 grams of solid samples are fixed to 10 milliliters and 2 grams are taken; 2 grams of liquid samples are taken), and the protein nitrogen content is measured by using this test paper, and then the nitrogen content is measured by the Kjeldahl method. See Table 1:
[0030] Table 1
[0031]
[0032] Then take the same sample and add 1% "melamine" according to the mass ratio, and use this test paper and the Kjeldahl method to detect the nitrogen content respectively. The results are shown...
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