Methods for the recovery of nucleic acids from a nucleic acid-containing material are provided, by which nucleic acids can be rapidly and easily recovered at a high purity without deteriorating the yield. The methods are composed of a step for promoting the release of nucleic acids from a nucleic ac
Methods for the recovery of nucleic acids from a nucleic acid-containing material are provided, by which nucleic acids can be rapidly and easily recovered at a high purity without deteriorating the yield. The methods are composed of a step for promoting the release of nucleic acids from a nucleic acid-containing material, a step for mixing the released nucleic acids with an accelerator substance for the binding of nucleic acids to a solid phase, a step for making the mixture in contact with a solid phase bondable to nucleic acids, a step for isolating the solid phase from a liquid, a step for washing the solid phase with a solution containing a salt, and a step for eluting the nucleic acids from the solid phase. Accordingly, nucleic acids at a suitable purity for genetic tests or gene analyses can be rapidly and easily recovered without the use of hazardous substances.
대표청구항▼
What is claimed is: 1. A method for purification of nucleic acids, comprising: mixing a nucleic acid-containing material with an accelerator substance containing a chaotropic substance for binding of nucleic acids to a solid phase; contacting the mixture of said nucleic acid-containing material an
What is claimed is: 1. A method for purification of nucleic acids, comprising: mixing a nucleic acid-containing material with an accelerator substance containing a chaotropic substance for binding of nucleic acids to a solid phase; contacting the mixture of said nucleic acid-containing material and said accelerator substance with the solid phase to bind nucleic acids to the solid phase; isolating the solid phase containing bound nucleic acids from the mixture; washing the solid phase containing bound nucleic acids with a solution containing a chaotropic substance and then washing said solid phase with a solution containing alcohol and acetate; and thereafter eluting the nucleic acids bound to the solid phase. 2. The method according to claim 1, wherein the alcohol is ethanol. 3. The method according to claim 1, wherein the acetate is solium acetate or potassium acetate. 4. The method according to claim 1, wherein the mixture of said nucleic acid-containing material and said accelerator substance is stirred with the solid phase at room temperature to bind the nucelic acids to the solid phase. 5. The method according to claim 1, wherein the solid phase is selected from the group consisting of glass beads, silica powder, quartz filter paper, quartz wool, diatomaceous earth, and crushed products of said glass beads, silica powder, quartz filter paper, or quartz wool. 6. The method according to claim 1, wherein said solid phase containing bound nucleic acids is washed with said solutions while maintaining said nucleic acids bound to said solid phase. 7. The method according to claim 1, wherein the solid phase includes particles having a particle size of about 1 to about 100 μm. 8. A method for recovery of nucleic acids from a material containing nucleic acids, which comprises: a step of mixing a nucleic acid-containing material with an accelerator substance containing a chaotropic substance for binding of nucleic acids to a solid phase containing silicon oxide; a step of contacting the mixture obtained in said mixing step with the solid phase containing silicon oxide to bind nucleic acids to the solid phase; a step of isolating the solid phase containing bound nucleic acids from the mixture; a step of washing the solid phase containing bound nucleic acids with a solution containing a chaotropic substance and then washing said solid phase with a solution containing alcohol and acetate; and a step of eluting the nucleic acids from the solid phase obtained after said washing step. 9. The method according to claim 8, wherein the alcohol is ethanol. 10. The method according to claim 8, wherein the acetate is sodium acetate or potassium acetate. 11. The method according to claim 8, which further comprises: a step of removing alcohol and acetate remaining in the eluted nucleic acids. 12. The method according to claim 8, wherein said contacting step includes stirring the mixture obtained in the mixing step with the solid phase at room temperature to bind the nucleic acids to the solid phase. 13. The method according to claim 8, wherein the solid phase is selected from the group consisting of glass beads, silica powder, quartz filter paper, quartz wool, diatomaceous earth, and crushed products of said glass beads, silica powder, quartz filter paper, or quartz wool. 14. The method of according to claim 8, wherein the washing step does not elute bound nucleic acids from the solid phase. 15. The method according to claim 8, wherein the solid phase includes particles having a particle size of about 1 to about 100 μm.
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이 특허에 인용된 특허 (4)
Kopaciewicz William ; Sheer Donald G. ; Arnold Todd E. ; Goel Vinay, Cast membrane structures for sample preparation.
Raybuck Margaret P. (Pontyclun Mid Glamorgan GBX) Kenrick Michael K. (Cardiff GBX) Parry David A. (London GBX), Device and method for affinity separation.
Boom Willem R. (Amsterdam NLX) Adriaanse Henritte M. A. (Arnhem NLX) Kievits Tim (The Hague NLX) Lens Peter F. (Amsterdam NLX), Process for isolating nucleic acid.
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