Almond mass spectrometric detection characteristic sequence group and detection kit
A characteristic sequence and mass spectrometry detection technology, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve problems such as false positive results of antibodies, shorten the detection time, meet the needs of a large number of screening and confirmation work, and meet the requirements of quantitative detection Effect
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[0047] Sample: The bread package is marked with a statement stating that it contains almond ingredients, and it is detected by mass spectrometry.
[0048] Take 2 g of bread matrix, add 10ml of extraction buffer, shake at 60°C for 3h, centrifuge at 14000g for 10min, take the supernatant, add 1M DTT solution 1μl, 37°C for 2h, then add 1M IAA 5μl at room temperature for 40min. After the reaction, directly add 2 μL trypsin (200 ng / μL) and hydrolyze with shaking at 37 °C for 1.5 hours.
[0049] After enzymolysis is completed, centrifuge at 20,000 g for 5 minutes, take the supernatant, and directly inject the sample for analysis.
[0050] Liquid chromatography conditions:
[0051] Column: Hypersil GOLD aQ column (100 x 2.1 mm, 1.9 μm); sample volume: 10 μL; phase A: 0.1% formic acid aqueous solution; phase B: 0.1% formic acid acetonitrile solution; flow rate: 300 μL / min; analytical gradient : 0 – 2 min 5% B, 2 – 12 min 5%–95% B, 12–17 min 95% B, 17–18 min, 95%–5% B, 18–23 min 5% B.
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