Method for detecting and identifying Cernuella virgata Da Costa by PCR
A snail and reaction technology, applied in the field of molecular biology detection and identification, can solve problems such as little knowledge of terrestrial mollusk classification, and achieve rapid and reliable detection and identification, high specificity, and strong practicability.
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Embodiment 1
[0016] Embodiment 1: Mediterranean white snail PCR primer specificity test
[0017] 1. Preparation of materials
[0018] The snails tested are as follows: Mediterranean white snail Cernuella virgata (Da Costa, 1778) (Australian specimen), Mediterranean white snail Cernuella virgata (Da Costa, 1778) (New Zealand specimen), wrinkled snail Camaena cicatricosa , Boling Samo Satsuma stenozona , Zhiba snail Bradybaena virgo virgo , garden snail Cepaea hortensis Tianshui baby snail Pupinidius tianshuiensis , cover big snail Helix pomatia , young stone ring rib snail Plectotropis lithina , isomorphic snail Bradybaena similaris , umbilical snail Aegista permellita ; short-snail Bradybaenabrevispira , Satsuma snail Satsuma uncopila , bright big snail Helix lucorum , Cystosnail Physa acuta , pizza tea snail Theba pisana .
[0019] The above-mentioned snails were intercepted in the national port quarantine or obtained through domestic investigation and col...
Embodiment 2
[0031] Embodiment 2: PCR detection sensitivity test of Mediterranean white snail
[0032] The Mediterranean white snail DNA stock solution (100 ng / μL) extracted in Example 1 was diluted into 10 ng / μL, 1 ng / μL, 100 pg / μL, 10 pg / μL, 1 pg / μL, 100 There are 7 different concentration gradients of fg / μL and 10 fg / μL.
[0033] PCR amplification reaction system: the total volume is 25 μL, including 12.5 μL of 2×Taq PCR MasterMix mixture, 0.5 μL of upstream and downstream primers, 3 μL of DNA template, and the rest with sterilized ddH 2 O make up. After mixing, put it into a PCR amplification instrument for amplification.
[0034] The PCR amplification reaction program was: 94°C pre-denaturation for 5 minutes; 94°C for 30s, 46°C for 30s, 72°C for 1min, 25 cycles; 72°C for 10min, and the reaction was terminated.
[0035] Detection and identification of PCR products: Take 10 μL of PCR products and electrophoresis on 1.5% agarose gel (containing ethidium bromide) at 130V for about 30...
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