최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
DataON 바로가기다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
Edison 바로가기다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
Kafe 바로가기국가/구분 | United States(US) Patent 등록 |
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국제특허분류(IPC7판) |
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출원번호 | US-0035725 (2011-02-25) |
등록번호 | US-8323900 (2012-12-04) |
발명자 / 주소 |
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출원인 / 주소 |
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대리인 / 주소 |
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인용정보 | 피인용 횟수 : 75 인용 특허 : 573 |
The present technology provides for an apparatus for detecting polynucleotides in samples, particularly from biological samples. The technology more particularly relates to microfluidic systems that carry out PCR on nucleotides of interest within microfluidic channels, and detect those nucleotides.
The present technology provides for an apparatus for detecting polynucleotides in samples, particularly from biological samples. The technology more particularly relates to microfluidic systems that carry out PCR on nucleotides of interest within microfluidic channels, and detect those nucleotides. The apparatus includes a microfluidic cartridge that is configured to accept a plurality of samples, and which can carry out PCR on each sample individually, or a group of, or all of the plurality of samples simultaneously.
1. An apparatus, comprising: a plurality of multi-lane microfluidic cartridges, each lane comprising a PCR reaction zone;a plurality of receiving bays, each receiving bay configured to receive one of the plurality of microfluidic cartridges;each PCR reaction zone comprising a separately controllable
1. An apparatus, comprising: a plurality of multi-lane microfluidic cartridges, each lane comprising a PCR reaction zone;a plurality of receiving bays, each receiving bay configured to receive one of the plurality of microfluidic cartridges;each PCR reaction zone comprising a separately controllable heat source thermally coupled thereto, wherein the heat source thermal cycles the PCR reaction zone to carry out PCR on a polynucleotide-containing sample in the PCR reaction zone and maintains a substantially uniform temperature throughout the PCR reaction zone during each cycle;a detector configured to detect the presence of an amplification product in one or more PCR reaction zones; anda processor coupled to the detector and the heat sources, configured to control heating of one or more PCR reaction zones by the heat sources. 2. The apparatus of claim 1, wherein the separately controllable heat source is configured to maintain a temperature gradient of less than 1° C. across a width of the PCR reaction zone at any point along a length of the PCR reaction zone. 3. The apparatus of claim 1, wherein the processor is programmable to operate the detector to detect a polynucleotide or a probe thereof in a plurality of microfluidic cartridges located in the plurality of receiving bays. 4. The apparatus of claim 1, wherein the detector comprises an optical detector, the optical detector comprising a light source that selectively emits light in an absorption band of a fluorescent dye and a light detector that selectively detects light in an emission band of the fluorescent dye, wherein the fluorescent dye corresponds to a fluorescent polynucleotide probe or a fragment thereof. 5. The apparatus of claim 4, wherein the optical detector comprises a bandpass-filtered diode that selectively emits light in the absorption band of the fluorescent dye and a bandpass filtered photodiode that selectively detects light in the emission band of the fluorescent dye. 6. The apparatus of claim 1, wherein the heat source comprises a plurality of heaters configured to maintain a substantially uniform temperature throughout a PCR reaction chamber thermally coupled to the heat source. 7. A device for carrying out PCR on a plurality of samples, the device comprising: a plurality of multi-lane microfluidic cartridges, each lane comprising a PCR reaction zone;a plurality of receiving bays, each receiving bay configured to receive one of the plurality of microfluidic cartridges;a separately controllable heat source thermally coupled to each PCR reaction zone, wherein the heat source is configured to thermal cycle the PCR reaction zone to carry out PCR on a polynucleotide-containing sample in the PCR reaction zone and to maintain a substantially uniform temperature throughout the PCR reaction zone during each cycle;a detector configured to detect the presence of an amplification product in one or more PCR reaction zones;a processor coupled to the detector and a plurality of the separately controllable heat sources, configured to control heating of one or more PCR reaction zones by one or more of the plurality of separately controllable heat sources; andan input device coupled to the processor and configured to permit concurrent or consecutive control of the plurality of multi-lane microfluidic cartridges. 8. The device of claim 7, wherein at least one of the plurality of separately controllable heat sources is a first contact heat source selected from a resistive heater, a radiator, a fluidic heat exchanger, and a Peltier device. 9. The device of claim 8, wherein the first contact heat source is thermally coupled to a distinct location in a first microfluidic cartridge received in a first receiving bay, whereby the distinct location is selectively heated. 10. The device of claim 9, wherein the distinct location has a surface area of between about 1 mm2 and about 225 mm2. 11. The device of claim 8, further comprising a second contact heat source configured to be independently thermally coupled to a distinct location in a second microfluidic cartridge received in a second receiving bay, whereby the distinct location in the second microfluidic cartridge is independently heated from the distinct location in the first microfluidic cartridge. 12. The device of claim 8, wherein the first contact heat source is configured to be in direct physical contact with the distinct location of the first microfluidic cartridge received in the first receiving bay. 13. The device of claim 8, further comprising a compliant layer configured to thermally couple the first contact heat source with at least a portion of the first microfluidic cartridge received in the first receiving bay. 14. The device of claim 7, wherein at least one of the plurality of separately controllable heat sources is a radiative heat source configured to direct heat to a distinct location of a first microfluidic cartridge received in a first receiving bay. 15. The device of claim 7, wherein the input device is selected from the group consisting of a keyboard, a touch-sensitive surface, a microphone, a hard disk drive, an optical disk drive, a serial connection, a parallel connection, a wireless network connection, a wired network connection, and a mouse. 16. The device of claim 7, further comprising at least one sample identifier coupled to the processor, the sample identifier being selected from an optical character reader, a bar code reader, and a radio frequency tag reader. 17. The device of claim 7, further comprising at least one output coupled to the processor, the output being selected from a display, a printer, a speaker, a serial connection, a parallel connection, a wireless network connection, and a wired network connection. 18. The device of claim 6, further comprising a heating stage configured to be removable from the device, wherein at least one of the plurality of separately controllable heat sources is located in the heating stage. 19. The device of claim 7, wherein the heat source comprises a plurality of heaters configured to maintain a substantially uniform temperature throughout a PCR reaction chamber thermally coupled to the heat source. 20. A method of carrying out PCR on a plurality of samples, the method comprising: introducing the plurality of samples into a plurality of multi-lane microfluidic cartridges, wherein each lane comprises a PCR reaction zone configured to permit thermal cycling of a sample independently of the other samples;moving the plurality of samples into the respective plurality of PCR reaction zones; andamplifying polynucleotides contained with the plurality of samples in the plurality of PCR reaction zones while thermal cycling the PCR reaction zones and maintaining a substantially uniform temperature throughout each PCR reaction zone during each cycle, at least one PCR reaction zone separately thermally controllable from another PCR reaction zone. 21. The method of claim 20, further comprising detecting the presence of a polynucleotide or a polynucleotide probe in the plurality of samples. 22. The method of claim 20, wherein thermal cycling the PCR reaction zones comprises heating each PCR reaction zone with a plurality of heaters configured to maintain a substantially uniform temperature throughout each PCR reaction zone.
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