Method for extracting DNA by echinoderm living body sampling
A technology for echinoderms and living organisms, which is applied in biochemical equipment and methods, determination/inspection of microorganisms, sugar derivatives, etc., and can solve the problems of lack of practical significance of genetic information and unfavorable genetic and breeding work of echinoderms.
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Embodiment 1
[0024] a. Put live sea urchins in a container filled with a small amount of seawater. The depth of seawater should be just submerged in sea urchins. In this way, the tube feet of sea urchins can protrude radially in the water, which is convenient for sampling; cut a small amount with scissors Sea urchin podia (according to the actual situation, about 1-3mm long podia can be obtained), put them on filter paper to absorb the water; weigh the quality of the sea urchin podia, the sampling volume should not be less than 0.01g, put them in 1.5ml centrifuge tube;
[0025] b. Add 200 μl of lysate to the centrifuge tube containing sea urchin podia, then cut or homogenize the tube podia in the lysate, digest at 50°C for 45-55 minutes, and oscillate once every 10 minutes during this period to ensure Ensure that the sample tissue is fully digested; the components and final concentration of the lysate are 0.2g / l proteinase K, 0.5% SDS, 100mmol / l EDTA, 0.05g / l RNase; because the content of ...
Embodiment 2
[0038] a. Put live sea cucumbers in a container filled with a small amount of seawater. It is advisable that the depth of seawater should be just submerged in sea cucumbers. Use scissors to cut out 1 to 3 tentacles (according to the size of sea cucumbers) or a few tube feet of sea cucumbers, and put them in Blot the water on the filter paper for later use; weigh the quality of the tube feet or tentacles of the sea cucumbers taken, and the sampling volume should not be less than 0.01g, and put them into a 1.5ml centrifuge tube; in order to prevent sea cucumbers from being infected due to tentacles or tube feet Add penicillin anti-inflammatory in seawater at the dosage of / L;
[0039] DNA was extracted according to steps b-1 of Example 1.
[0040] The results of electrophoresis showed by gel imaging that the concentration and quality of the DNA of the embodiment of the present invention were consistent with the DNA extracted from traditional (dead body) sampling tissues of echin...
Embodiment 3
[0042] a. Inject fresh water into the sea cucumber to stimulate the sea cucumber. The sea cucumber will excrete viscera at the same time as the injection. You can also inject 0.35mol / L KCl2~4mL, and the internal organs will be discharged after 1~2min; Rinse with double distilled water, then put the washed sea cucumber intestines on the filter paper to absorb the water; weigh the quality of the sea cucumber intestines taken, the sampling amount should not be less than 0.01g, and put them into a 1.5ml centrifuge tube;
[0043] Operate according to steps b~f;
[0044] After step f, observe the middle layer and the lower layer. If the middle layer or the lower layer is dark in color (unclear), add 400 μl of chloroform-isoamyl alcohol (24:1) and extract again.
[0045] Then follow steps g~l to extract DNA.
[0046] The results of electrophoresis showed by gel imaging that the concentration and quality of the DNA of the embodiment of the present invention were consistent with the D...
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