Method of tracing places of origin of aquatic products based on amino acid carbon stable isotopes
A carbon stable isotope, origin traceability technology, applied in measurement devices, instruments, scientific instruments, etc., can solve the problems of unconvincing, discrepancies, inaccurate identification results, etc., and achieve the effect of single composition and accurate identification results
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Embodiment 1
[0035] In April 2016, our laboratory collected samples of imitation japonicus from Fujian, Dalian and Shandong for testing. After the samples were refrigerated and transported back to the laboratory, they were immediately dissected, the viscera and lime ring were removed, the muscle part was washed with ultrapure water, and then placed in a -20°C refrigerator for 24 hours. Freeze-dry the completely frozen imitation japonicus muscle at -50°C for 24 hours, then grind it into a powder with a glass mortar without stable isotope interference, and store it dry.
[0036] The above-mentioned processed samples are tested according to the following steps:
[0037] 1. Amino acid extraction and purification: Take 20 mg of the sample and place it in a hydrolysis tube, add 2 mL of 6N hydrochloric acid, and pour N into the tube 2 , to completely replace the air therein, seal the tube, hydrolyze at 110 ° C for 24 h, centrifuge the obtained hydrolyzate at 430 g for 10 min, take the supernatan...
Embodiment 2
[0050] In June 2016, samples of Chlamys farreri and Ezo scallops were collected from Hebei, Shandong, Liaoning and Jiangsu for testing. After the samples were refrigerated and transported back to the laboratory, they were dissected immediately, the viscera and outer shell were removed, the adductor muscle part was selected and washed with ultrapure water, and then placed in a -20°C refrigerator for 24 hours. Freeze-dry the completely frozen imitation japonicus muscle at -50°C for 24 hours, then grind it into a powder with a glass mortar without stable isotope interference, and store it dry.
[0051] The above-mentioned processed samples are tested according to the following steps:
[0052] 1. Amino acid extraction and purification: Take 20 mg of the sample and place it in a hydrolysis tube, add 2 mL of 6N hydrochloric acid, and pour N into the tube 2 , until the air in it is completely replaced, seal the tube, hydrolyze at 110°C for 24 hours, centrifuge the obtained hydrolyza...
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