Nucleic acid preserving fluid, preparation method thereof and method for applying nucleic acid preserving fluid
A technology for preservation solution and nucleic acid, applied in the field of nucleic acid preservation, which can solve the problems of high production cost, cumbersome operation, and heavy workload of preservation solution, and achieve the effects of low cost, convenient preparation process and low production cost
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Embodiment 1
[0050] Example 1: Nucleic acid preservation solution, the components included and their corresponding dosages are shown in Table 1, and are prepared through the following steps:
[0051] Step 1, thoroughly mix trisodium citrate, biological buffer, disodium edetate and 30ml of pure water until completely dissolved to form the first mixture;
[0052] Step 2, add an acid-base regulator to the first mixture obtained in step 1, mix well, adjust the pH value to 3.5-4.0, then add preservative Proclin-300, and finally add pure water to 100ml to obtain nucleic acid preservation liquid.
[0053] Wherein, the concentration of triethanolamine hydrochloride is 400mmol / L, the concentration of N,N-bis(2-hydroxyethyl)-2-aminoethanesulfonic acid is 600mmol / L; the concentration of glacial acetic acid is 0.7mol / L, polyacrylic acid The concentration is 5wt%. In terms of bases, the length of a nucleic acid is 10,000 bases.
[0054] In addition, trisodium citrate, triethanolamine hydrochloride, ...
Embodiment 2-4
[0057] Example 2-4: Nucleic acid preservation solution, the difference from Example 1 is that the components included and their corresponding dosages are shown in Table 1.
Embodiment 5
[0058] Embodiment 5: Nucleic acid preservation solution, the difference from Example 1 is that in the biological buffer, the concentration of triethanolamine hydrochloride is 500mmol / L, N, N-bis(2-hydroxyethyl)-2-aminoethanesulfonic acid The concentration is 500mmol / L.
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