JPH1194747A - Biochip and biochip reader - Google Patents
Biochip and biochip readerInfo
- Publication number
- JPH1194747A JPH1194747A JP25480997A JP25480997A JPH1194747A JP H1194747 A JPH1194747 A JP H1194747A JP 25480997 A JP25480997 A JP 25480997A JP 25480997 A JP25480997 A JP 25480997A JP H1194747 A JPH1194747 A JP H1194747A
- Authority
- JP
- Japan
- Prior art keywords
- biochip
- spots
- circular
- dna
- fluorescent light
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/0046—Sequential or parallel reactions, e.g. for the synthesis of polypeptides or polynucleotides; Apparatus and devices for combinatorial chemistry or for making molecular arrays
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00277—Apparatus
- B01J2219/00497—Features relating to the solid phase supports
- B01J2219/00527—Sheets
- B01J2219/00529—DNA chips
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00277—Apparatus
- B01J2219/00497—Features relating to the solid phase supports
- B01J2219/00527—Sheets
- B01J2219/00531—Sheets essentially square
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00277—Apparatus
- B01J2219/00497—Features relating to the solid phase supports
- B01J2219/00527—Sheets
- B01J2219/00536—Sheets in the shape of disks
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00583—Features relative to the processes being carried out
- B01J2219/00596—Solid-phase processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00583—Features relative to the processes being carried out
- B01J2219/00603—Making arrays on substantially continuous surfaces
- B01J2219/00605—Making arrays on substantially continuous surfaces the compounds being directly bound or immobilised to solid supports
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00583—Features relative to the processes being carried out
- B01J2219/00603—Making arrays on substantially continuous surfaces
- B01J2219/00605—Making arrays on substantially continuous surfaces the compounds being directly bound or immobilised to solid supports
- B01J2219/00608—DNA chips
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00583—Features relative to the processes being carried out
- B01J2219/00603—Making arrays on substantially continuous surfaces
- B01J2219/00659—Two-dimensional arrays
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/0068—Means for controlling the apparatus of the process
- B01J2219/00702—Processes involving means for analysing and characterising the products
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
- B01J2219/00718—Type of compounds synthesised
- B01J2219/0072—Organic compounds
- B01J2219/00722—Nucleotides
-
- C—CHEMISTRY; METALLURGY
- C40—COMBINATORIAL TECHNOLOGY
- C40B—COMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
- C40B40/00—Libraries per se, e.g. arrays, mixtures
- C40B40/04—Libraries containing only organic compounds
- C40B40/06—Libraries containing nucleotides or polynucleotides, or derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は分子生物学全般で使
用されているDNAや蛋白質に蛍光物質を標識して、レ
ーザーで蛍光物質を励起し、蛍光の発光量でDNAや蛋
白質の量を検出する読取り方式で、読取りが安価で実現
可能な手法に関する。バイオチップはDNAや蛋白質を
高密度に集積して格納したものに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for labeling DNA or protein used in general molecular biology with a fluorescent substance, exciting the fluorescent substance with a laser, and detecting the amount of DNA or protein by the amount of fluorescence emitted. The present invention relates to an inexpensive and feasible reading method. The biochip relates to a device in which DNAs and proteins are stored at a high density.
【0002】[0002]
【従来の技術】従来のバイオチップは四角形状で、図6
に示すようなスポットが植え付けてある。2はスポット
で、17は蛍光標識されたDNAや蛋白質で、16は蛍
光物質である。バイオチップの読取りは、例えば図2に
示すようなものがある。図2において、1はバイオチッ
プで、2はバイオチップに蛍光物質が標識されたDNA
や蛋白質をスポットしたものであり、1のバイオチップ
を読取るために、5のレーザーを発信させ、6のミラー
でレーザー光を横軸に振り、2のスポットの蛍光物質を
励起させ、発光した蛍光を8の光ファイバーで集光し、
9の光学フィルタで目的の波長を抽出し、7のホトマル
で検出し、1のバイオチップを4の縦軸方向に駆動さ
せ、次のラインを読取り、これを繰り返してバイオチッ
プ全体を読取っていた。2. Description of the Related Art A conventional biochip has a quadrangular shape, and FIG.
Spots as shown in the figure are planted. 2 is a spot, 17 is a fluorescently labeled DNA or protein, and 16 is a fluorescent substance. The reading of the biochip is, for example, as shown in FIG. In FIG. 2, 1 is a biochip, and 2 is a DNA in which a fluorescent substance is labeled on the biochip.
In order to read 1 biochip, a laser 5 is emitted, and a laser beam is moved along a horizontal axis by a mirror 6 to excite a fluorescent substance in a spot 2 to emit fluorescent light. With 8 optical fibers,
The objective wavelength was extracted by the optical filter 9 and detected by the photomultiplier 7, the biochip 1 was driven in the direction of the vertical axis of 4, the next line was read, and this was repeated to read the entire biochip. .
【0003】[0003]
【発明が解決しようとする課題】しかしながら、このよ
うな従来の方法では、バイオチップを読取るのにチップ
を駆動させるメカニズムとレーザーを振って読取るライ
ンセンサーのメカニズムが必要となり、コストが高くな
り問題となっていた。However, in such a conventional method, a mechanism for driving a chip and a mechanism for a line sensor for reading by shaking a laser are required for reading a biochip. Had become.
【0004】本発明はチップの形状を円形状にし、読取
りは円盤を回転させ、ポイントセンサーで読取ること
で、低コストで読取りを可能とすることを目的とする。An object of the present invention is to make it possible to read at low cost by making a chip into a circular shape, reading by rotating a disk and reading by a point sensor.
【0005】[0005]
【課題を解決するための手段】図1は本発明の原理説明
図である。本発明は10のバイオチップを円形状に作成
し、11のモータで回転させ、18のポイントセンサ部
を、19の円の中心方向に駆動させて読むことを特徴と
する。FIG. 1 is a diagram illustrating the principle of the present invention. The present invention is characterized in that 10 biochips are formed in a circular shape, rotated by 11 motors, and 18 point sensor units are driven in the direction of the center of 19 circles for reading.
【0006】また、2のスポット内が化学発光で光って
いる光を読取るときは5のレーザーを切って読取り、蛍
光方式でも化学発光方式でも読取りができることを特徴
とする。[0006] Further, when reading light in which the inside of the spot 2 shines by chemiluminescence, reading is performed by turning off the laser 5 and reading can be performed by a fluorescent method or a chemiluminescent method.
【0007】このような方式によれば、回転式でバイオ
チップを読取ることができ、センサーもポイントセンサ
ーであるため、ラインセンサーに比べ安価に装置の実現
ができる。バイオチップの読取装置が安価であれば各研
究室で手軽にバイオチップを使用した実験ができるよう
になり、遺伝子解明の研究のスピードアップに役立つ。[0007] According to such a system, the biochip can be read in a rotating manner, and since the sensor is also a point sensor, an apparatus can be realized at lower cost than a line sensor. If the biochip reader is inexpensive, it will be possible to easily carry out experiments using the biochip in each laboratory, which will help speed up research on gene elucidation.
【0008】[0008]
【発明の実施の形態】以下、本発明の実施の形態を図面
に基づいて説明する。図6はスポット構造で、2はスポ
ット、17は標識されたDNAあるいは蛋白質、16は
蛍光物質のTexasRedである。図3はスポットがトラック
単位に順次並んでいるバイオチップで、2はスポット、
10はチップ全体である。チップの素材としてはガラス
を使用する。図4はスポットが同一角度で並んでいるバ
イオチップで、2はスポットで、10はチップ全体であ
る。図5はスポットが渦巻きの形で並んでいるバイオチ
ップで、2はスポットで、10は全体像である。図3、
図4及び図5はいずれも円盤型バイオチップの実施例を
示す図である。Embodiments of the present invention will be described below with reference to the drawings. FIG. 6 shows a spot structure, 2 is a spot, 17 is a labeled DNA or protein, and 16 is a fluorescent substance, TexasRed. FIG. 3 shows a biochip in which spots are sequentially arranged in track units.
10 is the whole chip. Glass is used as a chip material. FIG. 4 shows a biochip in which spots are arranged at the same angle, 2 is a spot, and 10 is the entire chip. FIG. 5 shows a biochip in which spots are arranged in a spiral, 2 is a spot, and 10 is a whole image. FIG.
4 and 5 are diagrams each showing an embodiment of a disc-shaped biochip.
【0009】図1は本発明の一実施の形態に係わる全体
構成図である。図1において、10は円盤型のバイオチ
ップであり、11のモーターで回転させる。18はポイ
ントセンサー部であり、5は半導体励起固体レーザーで
532nmのレーザー光を発信させ、13のダイクロイ
ックミラーでレーザー光の波長のみを2のスポットに向
けて反射させ、12のレンズでレーザー光を絞って、2
のスポットに照射し、スポット中のDNAや蛋白質に標識
している蛍光物質を励起し、蛍光を発光させる。12は
レンズで発光した蛍光を集光して平行光にし、13のダ
イクロイックミラーを通り抜け、625nmを選択的に
透過する光学干渉フィルター9で蛍光以外の光をカット
し、15のレンズで絞り込み、7のホトマルへ光を入れ
て検出する。FIG. 1 is an overall configuration diagram according to an embodiment of the present invention. In FIG. 1, reference numeral 10 denotes a disk-shaped biochip, which is rotated by a motor 11. Reference numeral 18 denotes a point sensor unit. Reference numeral 5 denotes a semiconductor-excited solid-state laser that emits 532 nm laser light, 13 dichroic mirrors reflect only the wavelength of the laser light toward 2 spots, and 12 lenses transmit laser light. Squeeze 2
The spot is irradiated to excite a fluorescent substance labeled on DNA or protein in the spot to emit fluorescence. Numeral 12 converges the fluorescent light emitted by the lens into parallel light, passes through a dichroic mirror 13, cuts off light other than fluorescent light with an optical interference filter 9 that selectively transmits 625 nm, and narrows down with a lens 15. Light is injected into the photomultiplier to detect.
【0010】なお、本発明において、化学発光でDNA
や蛋白質の標識を発光させたときは、5のレーザーを切
り、14の光学干渉フィルターを発光波長を選択的に透
過する光学干渉フィルターに変更し読取れば、蛍光方式
と同様に、10のバイオチップを読取ることができると
いう特長を有する。[0010] In the present invention, DNA is produced by chemiluminescence.
When the label of protein or protein is emitted, the laser of 5 is turned off, the optical interference filter of 14 is changed to an optical interference filter that selectively transmits the emission wavelength, and reading is performed. It has the feature that a chip can be read.
【0011】更に、チップの両面にDNAなどをスポット
し、読み取ることにより、少ない検体の量で、効率的に
読み取ることが可能である。Further, by spotting and reading DNA or the like on both sides of the chip, it is possible to read efficiently with a small amount of sample.
【0012】[0012]
【発明の効果】以上説明をしたように、本発明によれば
円盤型のバイオチップを回転して読めば、従来のレーザ
ー光を振って、光ファイバで集光して読む機構が不要と
なり、低コストで読取装置の実現ができる。As described above, according to the present invention, if a disk-shaped biochip is rotated and read, a conventional mechanism for shaking a laser beam and condensing it with an optical fiber to read it is unnecessary. A reading device can be realized at low cost.
【図1】本発明の原理説明図である。FIG. 1 is a diagram illustrating the principle of the present invention.
【図2】従来の説明図である。FIG. 2 is a conventional explanatory diagram.
【図3】スポットがトラック単位に順次並んでいるバイ
オチップである。FIG. 3 is a biochip in which spots are sequentially arranged in track units.
【図4】スポットが同一角度で並んでいるバイオチップ
である。FIG. 4 is a biochip in which spots are arranged at the same angle.
【図5】スポットが渦巻きの形で並んでいるバイオチッ
プである。FIG. 5 is a biochip in which spots are arranged in a spiral.
【図6】スポットの構造である。FIG. 6 shows a spot structure.
【符号の説明】 1…四角型バイオチップ、2…スポット、3…レーザー
光のスキャン方向、4…チップの駆動方向、5…レーザ
ー、6…振動ミラー、7…ホトマル、8…集光光ファイ
バー、9…光学フィルター、10…円型バイオチップ、
11…回転モーター、12…集光レンズ、13…ダイク
ロイックミラー、15…ホトマル用集光レンズ、16…
蛍光物質、17…DNAまたは蛋白質、18…ポイントセ
ンサー部、19…ポイントセンサー部の駆動方向。[Description of Signs] 1 ... Square biochip, 2 ... Spot, 3 ... Scanning direction of laser light, 4 ... Drive direction of chip, 5 ... Laser, 6 ... Vibrating mirror, 7 ... Photomaru, 8 ... Condensing optical fiber, 9 optical filter, 10 circular biochip,
11: rotating motor, 12: condensing lens, 13: dichroic mirror, 15: condensing lens for photomaru, 16 ...
Fluorescent substance, 17: DNA or protein, 18: Point sensor section, 19: Drive direction of the point sensor section.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 藤宮 仁 神奈川県横浜市中区尾上町6丁目81番地 日立ソフトウェアエンジニアリング株式会 社内 (72)発明者 百合野 以子 神奈川県横浜市中区尾上町6丁目81番地 日立ソフトウェアエンジニアリング株式会 社内 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Jin Fujimiya 6-81 Ouecho, Naka-ku, Yokohama-shi, Kanagawa Prefecture In-house Hitachi Software Engineering Co., Ltd. 81 Hitachi Software Engineering Co., Ltd.
Claims (3)
スポットしたことを特徴とするバイオチップ。1. A biochip comprising probe DNAs and proteins spotted in a circular array.
取ることを特徴とするバイオチップ読取り装置。2. A biochip reader characterized in that a circular biochip is rotated and read.
DNAや蛋白質に蛍光物質を標識し、レーザーで励起し
て読取る手段と、DNAや蛋白質を化学発光させて読取
る手段を備えたことを特徴とする読取り装置。3. The biochip reader according to claim 2, wherein
A reading device comprising: means for labeling DNA or protein with a fluorescent substance, exciting by laser and reading; and means for reading DNA or protein by chemiluminescence.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25480997A JP3346727B2 (en) | 1997-09-19 | 1997-09-19 | Biochip and biochip reader |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25480997A JP3346727B2 (en) | 1997-09-19 | 1997-09-19 | Biochip and biochip reader |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH1194747A true JPH1194747A (en) | 1999-04-09 |
JP3346727B2 JP3346727B2 (en) | 2002-11-18 |
Family
ID=17270195
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25480997A Expired - Fee Related JP3346727B2 (en) | 1997-09-19 | 1997-09-19 | Biochip and biochip reader |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3346727B2 (en) |
Cited By (21)
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---|---|---|---|---|
WO2000068668A1 (en) * | 1999-05-11 | 2000-11-16 | Hitachi Software Engineering Co., Ltd. | Method and device for fluorescence measurement |
WO2001016600A1 (en) * | 1999-08-31 | 2001-03-08 | Mitsubishi Chemical Corporation | Method of analyzing mutual interaction between protein and molecule |
WO2001038875A1 (en) * | 1999-11-19 | 2001-05-31 | Hitachi Software Engineering Co., Ltd. | Biochip reader and labeling reagent |
WO2001057180A1 (en) * | 2000-01-31 | 2001-08-09 | Matsushita Seiko Co., Ltd. | Kit for detecting microorganisms, apparatus for quanitifying microorganisms and method for quantifying microorganisms |
WO2002016915A1 (en) * | 2000-08-23 | 2002-02-28 | Sanyo Electric Co., Ltd | Chemical sensor and method of detecting chemical |
WO2003079013A1 (en) * | 2002-03-15 | 2003-09-25 | Sony Corporation | Bio-assay substrate, bio-assay apparatus, and reading apparatus |
WO2004025296A1 (en) * | 2002-08-30 | 2004-03-25 | Sony Corporation | Substrate for bioassay, substrate information reader, and substrate information reading method |
WO2004068125A1 (en) * | 2003-01-31 | 2004-08-12 | Universal Bio Research Co., Ltd. | Continuous optical measuring apparatus and continuous optical measuring method |
JP2004257737A (en) * | 2003-02-24 | 2004-09-16 | Mitsui Eng & Shipbuild Co Ltd | Biochip reader |
JP2004264068A (en) * | 2003-02-28 | 2004-09-24 | Institute Of Tsukuba Liaison Co Ltd | Bio-sensor chip |
WO2005033703A1 (en) * | 2003-10-03 | 2005-04-14 | Sony Corporation | Method for producing bioassay substrate by superposing two substrates one on another and bioassay substrate |
WO2005038053A1 (en) * | 2003-10-18 | 2005-04-28 | Nanostorage Co., Ltd. | Biochip analysis system and diagnosis system having biochip analysis apparatus |
WO2005050205A1 (en) * | 2003-11-11 | 2005-06-02 | Sony Corporation | Bioassay substrate on which feeder wiring is laid |
KR100529477B1 (en) * | 2002-11-19 | 2005-11-22 | 재단법인서울대학교산학협력재단 | CIS(CMOS Image Sensor) detecting method for detecting intensity of fluorescence light from a biochip |
EP1643239A1 (en) * | 2004-09-30 | 2006-04-05 | Yokogawa Electric Corporation | Screening apparatus |
US7045362B2 (en) | 2000-03-17 | 2006-05-16 | Harald Lossau | Device and method for detecting organic molecules in a test substance |
US7217573B1 (en) | 1999-10-05 | 2007-05-15 | Hitachi, Ltd. | Method of inspecting a DNA chip |
US7632463B2 (en) | 2003-12-05 | 2009-12-15 | Mitsubishi Kagaku Iatron, Inc. | Analysis apparatus and condenser |
EP2159567A1 (en) * | 2004-09-10 | 2010-03-03 | Wallac Oy | Enhanced instrumentation and method for optical measurement of samples |
US8119391B2 (en) | 2003-10-18 | 2012-02-21 | Nanostorage Co., Ltd. | Biochip analysis system |
CN113308357A (en) * | 2021-07-28 | 2021-08-27 | 中国农业大学 | Intelligent anti-pollution PCR tube fluorescence detection system |
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1997
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