Detection method of prawn IHHNV (infectious hypodermal and hematopoietic necrosis virus) and used nucleic acid isothermal amplification detection kit
A detection kit and isothermal amplification technology, applied in the direction of microbial determination/inspection, biochemical equipment and methods, etc., can solve the problems of limiting the popularization and application of PCR detection methods, low detection sensitivity, and inability to detect viruses, and reduce false positives. Positive results, good detection specificity, and less error-prone effects
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Embodiment 1
[0048] Embodiment 1, a kind of prawn IHHNV nucleic acid isothermal amplification detection kit (5 samples, can be used for the detection of 5 samples), it is made up of following content:
[0049] (1) Grinding solution tube, 1 tube, 3ml.
[0050] Grinding solution preparation: 10 parts of 1M Tris-HCl solution (Tris-HCl, pH8.0), 0.25M ethylenediaminetetraacetic acid disodium solution (EDTANa 2 ) 2 parts, 10 parts of sodium dodecylsulfonate solution (SDS) with a mass fraction of 5%, 0.5 part of mercaptoethanol, 0.01 part of 8-hydroxyquinoline, 7 parts of balanced phenol, 8 parts of chloroform, fixed with double distilled water Can hold up to 100 copies. The above parts are all parts by volume.
[0051] (2) Tube A of nucleic acid extraction solution, 1 tube, containing 400 μl of 3M sodium acetate solution (NaAc, pH 5.2).
[0052] (3) Tube B of nucleic acid extraction solution, 1 tube, filled with 10ml of absolute ethanol.
[0053] (4) Tube C of nucleic acid extraction solutio...
Embodiment 2
[0077] Embodiment 2. A prawn IHHNV nucleic acid isothermal amplification detection kit (5 samples), which is different from embodiment 1 only in the following content, and the rest are the same as embodiment 1.
[0078] Grinding solution preparation: 5 parts of 2M Tris-HCl solution (Tris-HCl, pH8.0), 0.5M ethylenediaminetetraacetic acid disodium solution (EDTANa 2 ) 1 part, 7 parts of sodium dodecylsulfonate solution (SDS) with a mass fraction of 7%, 0.01 part of mercaptoethanol, 0.02 part of 8-hydroxyquinoline, 5 parts of balanced phenol, 10 parts of chloroform, fixed with double distilled water Can hold up to 100 copies. The above parts are all parts by volume.
[0079] The composition of the LAMP reaction solution is as follows: LAMP primers IHHNV-FIP and IHHNV-BIP each 4 μM, LAMP primers IHHNV-F3 and IHHNV-B3 each 0.5 μM, dATP, dGTP and dCTP each 2 mM, dTTP, dUTP each 1.0 mM, Tris- HCl 40mM, KCl 20mM, (NH 4 ) 2 SO 4 15mM, MgSO 4 4mM, Triton X-100 1.0%, Betaine 0.8M...
Embodiment 3
[0080] Embodiment 3. A prawn IHHNV nucleic acid isothermal amplification detection kit (5 samples), which is different from Example 1 only in the following content, and the rest are the same as Example 1.
[0081] Grinding solution preparation: 7 parts of 1.5M Tris-HCl solution (Tris-HCl, pH8.0), 1.0M ethylenediaminetetraacetic acid disodium solution (EDTANa 2 ) 0.5 part, 5 parts of sodium dodecylsulfonate solution (SDS) with a mass fraction of 10%, 0.01 part of mercaptoethanol, 0.015 part of 8-hydroxyquinoline, 10 parts of balanced phenol, 10 parts of chloroform, fixed with double distilled water Can hold up to 100 copies. The above parts are all parts by volume.
[0082] The composition of the LAMP reaction solution is as follows: LAMP primers IHHNV-FIP and IHHNV-BIP each 1 μM, LAMP primers IHHNV-F3 and IHHNV-B3 each 0.25 μM, dATP, dGTP and dCTP each 0.5 mM, dTTP, dUTP each 0.5 mM, Tris -HCl 40mM, KCl 10mM, (NH 4 ) 2 SO 4 5mM, MgSO 4 1mM, Triton X-1000.05%, Betaine 0...
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