Apparatus, system, and method for purifying nucleic acids
Methods and devices for isolating nucleic acids from a mixture containing such nucleic acids and extraneous matter are provided. In one embodiment, the method of the invention comprises passing the mixture through a glass frit under conditions effective to separate the nucleic acids from the extraneous matter. In a more specific embodiment, the glass frit is a sintered glass frit.
1. A device for isolating nucleic acids from a mixture containing such nucleic acids and extraneous matter, comprising:
a hollow chamber having disposed therein at least one glass frit that is capable of binding to said nucleic acids in a cell lysate prepared by lysing cells outside said glass frit, said glass frit being arranged within said hollow chamber such that said mixture flows through said glass frit when said mixture is flowed through said hollow chamber, and said glass frit having a pore size of between about 2 microns and about 20 microns,
wherein said glass frit comprises a rigid, self-supporting frit structure with a thickness of about 1-20 mm and wherein said glass frit is not modified with a material with nucleic acid affinity.
2. The device of claim 1 , wherein said glass frit is a sintered glass frit.
3. The device of claim 2 , further comprising a heating device configured to heat said glass frit.
4. The device of claim 1 , wherein said glass frit has a pore size between about 10 microns and about 15 microns.
5. A fluidic device for identifying one or more nucleic acids from a mixture of such nucleic acids and extraneous matter, comprising: an inlet, an outlet, and at least one fluidic reaction chamber intermediate said inlet and said outlet and in communication with each of said inlet and said outlet; said device further comprising at least one glass fit arranged at a location proximal to said inlet and said at least one reaction chamber and in fluidic communication with each of said inlet and at least one fluidic reaction chamber, said glass frit having a pore size of between about 2 microns and about 20 microns and being capable of binding to said one or more nucleic acids in a cell lysate prepared by lysing cells outside said glass frit, such that said mixture enters said device through said inlet and passes through said glass frit to exit therefrom as a filtered product before entering said at least one fluidic reaction chamber; at least one fluidic reagent dispenser arranged intermediate said glass frit and said at least one reaction chamber, said at least one fluidic reagent dispenser being in fluidic communication with said at least one fluidic reaction chamber, wherein said glass frit comprises a rigid, self-supporting frit structure with a thickness of about 1-20 mm and wherein said glass frit is not modified with a material with nucleic acid affinity.
6. The device of claim 5 , wherein said at least one glass frit includes at least one sintered glass frit.
7. The device of claim 5 , wherein said at least one glass frit includes at least one glass frit having a pore size between about 10 microns and about 15 microns.
8. The device of claim 5 , further comprising a heater proximal to at least one said at least one glass frit.