Deer fetus DNA identification kit and method
An identification method and a technology of a detection kit, which are applied in the field of deer fetal DNA identification kits and identification, can solve the problems of cumbersome operation and inability to accurately identify the authenticity, and achieve reliable detection results
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Embodiment 1
[0059] 1. Pretreatment of test samples
[0060] There are two types of test samples, 1 is genuine deer fetus (fresh), and 2 is genuine deer fetus (dry), both provided and identified by Longtan Mountain Deer Industry Company in Jilin City). Take 1g for each, scrub and rinse with deionized water , dried at room temperature, and irradiated with ultraviolet light for more than 30 minutes. Use a mortar to grind the sample to about 2-3 mm, place it in a centrifuge tube, add the corresponding volume of treatment solution (mainly containing sucrose, Tris-HCl, Na 2 EDTA), shaking in a 56°C incubator for 4h. After centrifugation at 12000r / min for 10min, the supernatant was discarded, and the pellet was used for later use.
[0061] 2. Mitochondrial DNA Extraction
[0062] (1) Sample lysis Add 5ml of lysate to the pretreated sample, place it in a water bath, and shake it in a water bath at 56°C for 4 hours.
[0063] (2) Precipitation Add 2ml of precipitation solution directly to the l...
Embodiment 2
[0077] Example 2 Identification of Commercially Available Deer Fetus Medicinal Materials
[0078] 1. Materials
[0079] 2 samples of commercially available deer fetus powder, 2 genuine deer fetuses (provided and identified by Longtan Mountain Deer Industry Company in Jilin City); counterfeit sheep fetuses, pig fetuses, and cow fetuses (provided by Longtan Mountain Deer Industry Company in Jilin City), mutton , pork and beef (purchased from RT-Mart Supermarket in Jilin City).
[0080] 2. Method
[0081] 2.1 Pretreatment of test samples Take 1g of each test sample, put it in a centrifuge tube, add the corresponding volume of treatment solution (mainly containing sucrose, Tris-HCl, Na 2 EDTA), shaking in a 56°C incubator for 4h. After centrifugation at 12000r / min for 10min, the supernatant was discarded, and the pellet was used for later use.
[0082] 2.2 Mitochondrial DNA extraction
[0083] (1) Sample lysis Add 5ml of lysate to the pretreated sample, place it in a water ...
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