Identification primers, kit and identification method for tridacna crocea, tridacna maxima and first filial generation of tridacna crocea and tridacna maxima
A technology of safranaceus and identification method, which is applied in the directions of biochemical equipment and methods, microbial determination/inspection, DNA/RNA fragments, etc. Low cost, intuitive results, simple method effect
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[0023] A small amount of mantle tissue was cut from the foot silk pores of Tridacna safranatum, Tridacna longis and their hybrids, and 40 individuals of each of 40 individuals of Tridacna safranus, Tridacna longis and their hybrids were extracted by phenol-chloroform extraction. Genomic DNA. Specifically, shred the mantle tissue fully, absorb the water with clean filter paper, put it into a 1.5mL centrifuge tube, then add 400μl lysate and 10μl proteinase K (10mg / ml), mix well on a shaker, and store at 50°C Digest in a water bath for 3 to 5 hours until the lysate is clear. Add an equal volume of saturated phenol (200 μL), chloroform / isoamyl alcohol (24:1) (200 μL) mixture and extract three times. Precipitate DNA with 1 mL of absolute ethanol, wash with 70% alcohol, dry at room temperature and dissolve in 100 μL of ultrapure water. The concentration and purity of DNA were detected by ultraviolet spectrophotometer, and the integrity of DNA was detected by 1% agarose gel electro...
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