High-stability inactivated virus preserving fluid and preparation method thereof
A high-stability, preservation solution technology, applied in the medical field, can solve problems such as the integrity of virus nucleic acid needs to be improved, nucleic acid damage, etc., to achieve the effect of improving protection efficiency, improving research utility, and ensuring integrity
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Embodiment 1
[0026] A highly stable inactivated virus preservation solution, including lysis salt, RNase enzyme inhibitor, tromethamine, ethylenediaminetetraacetic acid, glycerol, nucleic acid protection peptide, water, and the RNase enzyme inhibitor includes iso Guanidine Thiocyanate, Phenol, Sodium Citrate, Dithiothreitol, and Sodium Lauroyl Sarcosinate;
[0027] The weight ratio of each component in the RNase enzyme inhibitor is: 16 parts of guanidine isothiocyanate, 2 parts of phenol, 10 parts of sodium citrate, 1 part of dithiothreitol, and 1 part of sodium lauroyl sarcosinate;
[0028] The protection solution is composed of the following proportions by weight: including 9 parts of cleavage salt, 20 parts of RNase inhibitor, 14 parts of tromethamine, 3 parts of ethylenediaminetetraacetic acid, 10 parts of glycerin, 6 parts of nucleic acid protection peptide, 100 parts of water.
Embodiment 2
[0030] A highly stable inactivated virus preservation solution, including lysis salt, RNase enzyme inhibitor, tromethamine, ethylenediaminetetraacetic acid, glycerol, nucleic acid protection peptide, water, and the RNase enzyme inhibitor includes iso Guanidine Thiocyanate, Phenol, Sodium Citrate, Dithiothreitol, and Sodium Lauroyl Sarcosinate;
[0031] The weight ratio of each component in the RNase enzyme inhibitor is: 16 parts of guanidine isothiocyanate, 2 parts of phenol, 10 parts of sodium citrate, 1 part of dithiothreitol, and 1 part of sodium lauroyl sarcosinate;
[0032] The protection solution is composed of the following proportions by weight: including 9 parts of cleavage salt, 20 parts of RNase inhibitor, 14 parts of tromethamine, 3 parts of ethylenediaminetetraacetic acid, 10 parts of glycerin, 6 parts of nucleic acid protection peptide, 100 parts of water;
[0033] The method for preparing the above-mentioned inactivated virus preservation solution is characteri...
Embodiment 3
[0038] A highly stable inactivated virus preservation solution, including lysis salt, RNase enzyme inhibitor, tromethamine, ethylenediaminetetraacetic acid, glycerol, nucleic acid protection peptide, water, and the RNase enzyme inhibitor includes iso Guanidine Thiocyanate, Phenol, Sodium Citrate, Dithiothreitol, and Sodium Lauroyl Sarcosinate;
[0039]The weight ratio of each component in the RNase enzyme inhibitor is: 16 parts of guanidine isothiocyanate, 2 parts of phenol, 10 parts of sodium citrate, 1 part of dithiothreitol, and 1 part of sodium lauroyl sarcosinate;
[0040] The protection solution is composed of the following proportions by weight: including 9 parts of cleavage salt, 20 parts of RNase inhibitor, 14 parts of tromethamine, 3 parts of ethylenediaminetetraacetic acid, 10 parts of glycerin, 6 parts of nucleic acid protection peptide, 100 parts of water;
[0041] The method for preparing the above-mentioned inactivated virus preservation solution is characteriz...
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