PCR detection kit for zaocys dhumnades
A technology of black snake and kit, applied in the field of identification of traditional Chinese medicine and Chinese medicinal materials
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Embodiment 1
[0021] Embodiment 1: the configuration of black-headed snake PCR detection kit
[0022] This embodiment provides 10 detection times and storage conditions of various components, and the specific quantity configured in the kit can be adjusted according to needs during specific implementation.
[0023]
[0024] Note: The working concentration of 50×TAE buffer is 1×TAE buffer; all reagents should be stored according to the specified conditions; 2×Taq PCR Green Mix is recommended to be aliquoted in small quantities to avoid repeated freezing and thawing.
Embodiment 2
[0025] Embodiment 2: the detection method of black snake kit
[0026] The detection method of the above kit comprises the following steps:
[0027] 2.1 DNA extraction
[0028] 2.1.1 Preparation before experiment
[0029] Prepare a clean mortar, pestle and spoon
[0030] Add all the RNase solution (for removing RNA) to the nucleus lysate Ⅰ and store at 4°C
[0031] Add 24ml of 95% absolute ethanol to the eluent, mark the bottle and store it at room temperature
[0032] 2.1.2 Template DNA extraction
[0033] ①Take an appropriate amount (about 0.5g) of the test sample, remove surface pollutants, grind it fully in liquid nitrogen to make powder, and take an appropriate amount (0.1ml scale) into a 1.5ml centrifuge tube;
[0034] ② Add 255 μl of cell nucleus lysate I (for lysing cell walls, etc.), and mix well;
[0035] ③ Add 20 μl proteinase K and mix well;
[0036] ④ Place it in a 55°C water bath and incubate for 1 hour;
[0037] ⑤ After taking it out, add 250 μL lys...
Embodiment 3
[0063] Embodiment 3: the preparation of PCR control substance
[0064] 3.1 PCR amplification with universal primers
[0065] Using the universal primer WS_ty_F: GGCCAGCAGCAGTAGTTAATATTAG; WS_ty_R:
[0066] TGGCGACGGCGGTATATAGACT amplified the total DNA of genuine black snake snake and counterfeit chinchilla snake respectively. Primers were synthesized by Huada Gene Technology Co., Ltd.
[0067] Perform PCR reactions in 200 µL centrifuge tubes. The total reaction volume was 25 μL, including 2.5 μL of 10×PCR buffer, dNTP (2.5 mmol L -1 ) 2 μL, universal primer (10 μmol L -1 ) each 0.5μL, Ex Taq DNA polymerase (5U·L -1 ) 0.2 μL, template 0.5 μL, make up the reaction volume with sterile double distilled water. Put the centrifuge tube into the PCR machine, and the PCR reaction parameters: pre-denaturation at 94°C for 5 minutes, cycle reaction 35 times (94°C for 30s, 56°C for 30s, 72°C for 30s), extension at 72°C for 5 minutes, and incubation at 4°C to end the reaction. Take ...
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