IP Library Granted Patent US 9,464,316
Granted Patent B2
US 9,464,316 · App. 14/035,890 · Granted Oct 11, 2016

Method for isolating nucleic acids comprising the use of ethylene glycol multimers

Inventor: Erling Sigurd Finne (Hvalstad, NO)
Assignee: Life Technologies AS
C12Q1/6806C12N15/1013
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Quick Facts
Patent No.
US 9,464,316
App. No.
14/035,890
Granted
Oct 11, 2016
Kind
B2
Abstract

A method of isolating nucleic acid from a sample is provided that includes contacting a sample that includes nucleic acid with a solid support, wherein the surface of the solid support includes groups that can complex with the nucleic acid, in the presence of a solution that includes an oligoethylene glycol having 10 or fewer ethylene oxide-units and a salt comprising a monovalent or divalent metal ion, whereby soluble nucleic acid in said sample binds to the surface of the support; separating the solid support with bound nucleic acid from the sample; and eluting the bound nucleic acid from the solid support, thereby isolating nucleic acid from the sample. Also provided is a method of washing nucleic acids bound to a solid support that includes providing a solid support, wherein nucleic acid molecules are bound to the surface of the solid support; and washing the solid support with a solution that includes an oligoethylene glycol having 10 or fewer ethylene oxide units.

Claims (21)

1. A method of isolating nucleic acid from a sample, said method comprising:

contacting a sample that comprises nucleic acid with a solid support having a hydrophilic surface that is neutral or has a net negative charge when the method is performed at a pH of 4 to 9, wherein the surface of the solid support comprises groups that can complex with the nucleic acid, in the presence of a solution comprising tetraethylene glycol and a salt comprising a monovalent or divalent metal ion, whereby soluble nucleic acid in said sample binds to the surface of the support;

separating the solid support with bound nucleic acid from the sample; and

eluting the bound nucleic acid from the solid support, thereby isolating nucleic acid from the sample.

2. A method of claim 1 wherein said sample is contacted with the tetraethylene glycol at a final concentration of greater than 15%.

3. A method of claim 1 further comprising binding said nucleic acid to said solid support in the presence of the salt comprising a monovalent or divalent metal ion at a final concentration of less than 1 M.

4. A method of claim 1 , further comprising performing said method in the presence of ethanol at a final concentration of less than 30% (v/v).

5. A method of claim 1 , further comprising contacting said sample with a detergent before, simultaneously or after contact of said sample with the tetraethylene glycol and said detergent is present at a final concentration of 0.2 to 30% (w/v).

6. A method of claim 5 wherein said detergent is an anionic detergent.

7. A method of claim 1 , further comprising performing the method in the presence of less than 1% (w/v) detergent and less than 30% (v/v) ethanol.

8. A method of claim 7 , further comprising performing the method in the presence of less than 0.2% (w/v) detergent and less than 10% (v/v) ethanol.

9. A method of claim 8 , further comprising contacting the sample with a buffer solution comprising the tetraethylene glycol-and the salt comprising a monovalent or divalent metal ion, wherein the buffer solution does not comprise a chaotrope.

10. A method of claim 7 , further comprising binding nucleic acid molecules of greater than 100 base pairs bind to the solid support and oligonucleotides of less than 30 nucleotides remain soluble in the solution.

11. A method of claim 1 , further comprising sequencing the eluted nucleic acid.

12. A method of claim 1 wherein said nucleic acid is DNA.

13. A method of claim 1 wherein said solid support is particulate.

14. A method of claim 1 , further comprising contacting the sample with a solid support that comprises magnetic beads.

15. A method of claim 1 , further comprising contacting said sample with a solid support that carries hydroxyl, epoxy, carboxylic acid or sulfonic acid groups.

16. A method of washing nucleic acids bound to a solid support, comprising:

providing a solid support having a hydrophilic surface that is neutral or has a net negative charge when the method is performed at a pH of 4 to 9, wherein nucleic acid molecules are bound to the surface of the solid support; and

washing the solid support with a solution comprising tetraethylene glycol.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 17, 2013
From: FINNE, ERLING SIGURD
To: INVITROGEN DYNAL AS
Reel/Frame 031803/0990 →
CHANGE OF NAME Recorded Dec 17, 2013
From: INVITROGEN DYNAL AS
To: LIFE TECHNOLOGIES AS
Reel/Frame 031804/0006 →
Priority Claims (2)
GB 0502887.3 · Feb 11, 2005 · national
GB 0503339.4 · Feb 17, 2005 · national
Continuity (3)
Continuation 11815964
Provisional Application 60654958 · Feb 23, 2005
Related Publication 20140094597A1 · Apr 3, 2014