Primer for multi-PCR (Polymerase Chain Reaction) recognition of bungarus multicinctus medicinal material, standard decoction and traditional Chinese medicine formula granules as well as application and recognition method of primer
A technology of traditional Chinese medicine formula granules, money white snake, applied in biochemical equipment and methods, recombinant DNA technology, microbial determination/inspection, etc. , Overcome the effect of the interference of excipients
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Embodiment 1
[0086] Example 1 Primer Design
[0087]Based on the NADH; Cytochrome Oxidase I; 12SrRNA; 16S rRNA; Cytochrome b sequence analysis of the Chinese Pharmacopoeia 2020 edition and common snake species, the homology comparison of the Cytochrome Oxidase I sequences of common snake species in the GeneBank database was performed using BioEdit software Yes, after proofreading, analyze the specific SNP site of Snake chrysalis, import the base sequence containing the SNP site into the Primer Premier 5 software, and design primers.
[0088] After sequence comparison, it was found that the specific site of the golden snake is T and the others are C. After determining the SNP site, make the SNP site close to the 3' end of the forward primer, and adjust the primer score and GC content by moving the position of the upstream primer , and with the help of Primer Premier 5 software, further adjust the position of the reverse primer, and determine the best combination through the final primer sco...
Embodiment 2
[0096] Embodiment 2 identification method is established
[0097] (1) DNA extraction and concentration adjustment
[0098] Take 0.5 g of dried sample, grind it into powder, put it in a 2 mL centrifuge tube, add 1.5 mL of CTAB precipitation solution preheated at 56 °C, 20 μL of proteinase K, mix well, heat in a water bath at 56 °C for 60 min, cool to room temperature, and use Centrifuge at 10000r / min for 5min, discard the supernatant, then add 900μL CTAB precipitation solution, 20μL proteinase K, and operate in the same way. Add 900 μL CTAB extract and 10 μL β-mercaptoethanol to the centrifuge tube successively, mix well, heat in a water bath at 65°C for 120 min, centrifuge, and take the supernatant after cooling to room temperature; add an equal volume of chloroform-isoamyl alcohol (24: 1), shake for 3 minutes, mix well; then centrifuge at 12000r / min, 4°C for 10 minutes, take 750 μL of the supernatant and add it to a new 2mL centrifuge tube, add an equal volume of chloroform-...
Embodiment 3
[0110] Embodiment 3 identification method verification
[0111] All kinds of samples of white snake, red chain snake and golden krait were taken (as shown in Table 1).
[0112] The identification method established in Example 2 was used to identify the samples. Wherein, in the PCR system, the amount of DNA template is 50ng.
[0113] Table 1 Sample sheet
[0114]
[0115]
[0116] Identification results such as figure 1 As shown, it can be seen from the figure that the medicinal materials of white snakes, standard decoction (freeze-dried powder) of snakes, traditional Chinese medicine formula granules of snakes, and the mixture containing snakes medicinal materials, standard decoction containing snakes There is a band of 160bp in all the mixtures of snakes; while other snake samples do not get this band. It can be seen from the figure that there is a band of 207bp in the red chain snake medicinal material, the red chain snake standard decoction (freeze-dried powder), ...
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