Xyleborus sp insect gene barcode detection kit and detection method thereof
A detection kit and barcode technology, which is applied in biochemical equipment and methods, microbiological determination/inspection, DNA/RNA fragments, etc., can solve many problems, and meet the needs of simple operation, lower sample quality, and amplification high efficiency effect
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Embodiment 1
[0043] Embodiment 1, a gene barcode detection kit for the genus Beetle insects, comprising a gene barcode sequence disc and a primer reagent with an amount of more than 10 times The primer sequence is as follows:
[0044] Upstream primer C1-J-2183 (5 , -CAACATTTATTTTTGATTTTTTGG-3 , )
[0045] Downstream primer TL2-N-3014 (5 ,-TCCAATGCACTAATCTGCCATATTA-3 , )
[0046] The gene barcode sequence disk has 37 standard barcode sequences, the sequences of which are shown in sequence 3-sequence 39 in the gene sequence table, and are suitable for the detection of the following 12 kinds of barcode insects:
[0047] Table 1 Names of species
[0048]
[0049] Its matching components also include the following reagents with an amount of more than 10 times: Taqbuffer, MgC1 2 , dNTPmix, TaqDNA polymerase, ddH 2 O, DNA template.
Embodiment 2
[0050] Embodiment 2, method for detecting the barcode of the insect gene of the genus Brutus:
[0051] Seven samples of red wood beetle, bamboo beetle, broad-faced wood beetle, double-spined long beetle, single-cut wood beetle, four-grain beetle, and chestnut-grain beetle were selected as the samples to be tested. Adopt the kit detection of embodiment 1, the steps are as follows:
[0052] (1) Extraction of DNA: The total DNA was extracted by conventional proteinase K digestion. The extraction steps are as follows:
[0053] Put the worm body (place) into an appropriate amount of distilled water, shake it properly, replace the alcohol in the worm body, and then place the worm body on absorbent paper to absorb the water on the worm body surface; put the worm body into a 1.5ml centrifuge Grind the tube quickly with a special small pestle; add 100 μL of non-toxic CTAB separation buffer (PH8.3), grind, then add 100 μL of the above separation solution, and continue grinding until t...
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