KR100443641B1 - DNA stealth pin manufacture method - Google Patents
DNA stealth pin manufacture method Download PDFInfo
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- KR100443641B1 KR100443641B1 KR10-2001-0059249A KR20010059249A KR100443641B1 KR 100443641 B1 KR100443641 B1 KR 100443641B1 KR 20010059249 A KR20010059249 A KR 20010059249A KR 100443641 B1 KR100443641 B1 KR 100443641B1
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
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- 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
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- 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
- B01J2219/00351—Means for dispensing and evacuation of reagents
- B01J2219/00364—Pipettes
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- 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
- B01J2219/00351—Means for dispensing and evacuation of reagents
- B01J2219/00373—Hollow needles
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- 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
- B01J2219/00457—Dispensing or evacuation of the solid phase support
- B01J2219/0047—Pins
Abstract
본 발명은 DNA 시료를 채취하여 일정용적을 취하는 DNA 함침 핀의 제조방법에 관한 것으로, 용접에 의해 접착되는 제 1접착면과, 상기 제 1접착면과 일정 곡률반경으로 굴곡되어 DNA 시료를 용적하는 제 1굴곡면과, 상기 제 1굴곡면과 일정 곡률반경으로 굴곡되어 DNA 함침 핀의 가장자리에 일정한 간격을 유지하는 제 1평탄면을 형성하는 몸체와, 상기 몸체에 면 대향되게 제 2접착면, 제 2굴곡면, 제 2평탄면을 형성하는 핀부재를 분리하여 가공하는 가공공정과, 상기 제 1평탄면과 제 2평탄면 사이에 미세간격이 형성되고, 한 쌍의 제 1굴곡면과 제 2굴곡면이 DNA 시료를 용적할 수 있는 수용부가 형성되도록 핀부재의 제 2접착면을 몸체의 제 1접착면에 밀착시켜 조립하는 조립공정과, 상호 밀착되어 있는 제 1접착면과 제 2접착면이 고정될 수 있도록 용접하는 용접공정으로 이루어져, DNA 함침 핀의 가장자리에 형성되는 미세간격을 몸체에 조립되는 핀부재를 이용하여 미세하게 조절할 수 있으므로 DNA 함침 핀의 정밀도를 향상시킨다.The present invention relates to a method for producing a DNA impregnating pin that takes a DNA sample and takes a certain volume. A body forming a first curved surface and a first flat surface curved at a predetermined radius of curvature with the first curved surface to maintain a predetermined distance at the edge of the DNA impregnation pin, and a second adhesive surface facing the body; A process of separating and processing the pin member forming the second curved surface and the second flat surface, and a fine gap is formed between the first flat surface and the second flat surface, and the pair of first curved surface and the first (2) an assembling process of assembling the second bonding surface of the pin member against the first bonding surface of the body so that the curved surface can accommodate the DNA sample, and the first bonding surface and the second bonding adhered to each other. For welding so that the face can be fixed It is made of a contact process, so that the micro-gaps formed at the edge of the DNA impregnation pin can be finely adjusted using a pin member assembled to the body, thereby improving the precision of the DNA impregnation pin.
Description
본 발명은 DNA 함침 핀의 제조방법에 관한 것으로, 보다 더 상세하게는 DNA 시료를 채취하여 일정용적을 취하는 DNA 함침 핀을 내구성이 강한 소재를 사용하여 정밀하게 가공하기 위한 DNA 함침 핀의 제조방법에 관한 것이다.The present invention relates to a method for producing a DNA impregnated pin, and more particularly to a method for producing a DNA impregnated pin for precisely processing a DNA impregnated pin taking a predetermined volume of DNA sample using a durable material. It is about.
최근, 유전학 및 단백질 연구분야에서는 DNA 시료가 순서대로 잘 정열되어 있는 마이크로 어레이 사용이 폭발적으로 증가하고 있다.Recently, in the field of genetics and protein research, the use of microarrays in which DNA samples are arranged in order is exploding.
상기 마이크로 어레이는 염기결합 법칙에 근거하여 알려지거나 알려지지 않은 유전자들을 결합시키는 매개체이고, 알려지지 않은 유전자를 밝혀내는 과정을 자동화하는 매개체를 제공하는 것으로, 유리판(glass) 위, 또는 나일론 멤블레이너(nylon membrane) 상에 DNA 함침 핀으로 수천개의 스팟(Spot)을 찍어 제작되며, 알고있는 프로우브(probe)를 사용하여 상보적인 결합을 탐색함으로써 동시에 대량의 유전자 발현과 유전자 탐색 등의 연구를 가능하게 한다.The microarray is a mediator that binds known or unknown genes based on the base binding law, and provides a mediator that automates the process of uncovering unknown genes. The microarray is on a glass or nylon nylon. Thousands of spots are made by DNA impregnating pins on the membrane, and the probe can be used to search for complementary binding using known probes. .
상기 DNA 함침 핀은 DNA 시료를 채취하여 일정용적을 취하는 초정밀 부품으로, 종래의 DNA 함침 핀을 도 1과 같이 설명하면 다음과 같다.The DNA impregnation pin is an ultra-precision component taking a DNA sample and taking a predetermined volume. Referring to FIG. 1, a conventional DNA impregnation pin is as follows.
도 1을 참조하면, 종래의 DNA 함침 핀는 한쌍의 핀부재(11a, 11b)가 일체로 형성되어 있으며, 상기 한쌍의 핀부재(11a, 11b)는 서로 면 대향되게 입출부(12)를 형성하고, 상기 입출부(12)에서 일정 곡률 반경으로 굴곡되어 있는 수용부(13)를 형성한다.Referring to FIG. 1, in the conventional DNA impregnation pin, a pair of pin members 11a and 11b are integrally formed, and the pair of pin members 11a and 11b form the entry and exit portions 12 facing each other. In addition, the receiving part 12 forms a receiving part 13 which is bent at a predetermined radius of curvature.
상기 입출부(12)는 상기 한쌍의 핀부재(11a, 11b)의 외측에서 내측으로 압축하여 상기 입출부(12)의 미세간격을 조절하며, 상기 수용부(13)는 DNA 시료의 함침량에 따라 직선형, 유선형 등 다양한 형태로 제작될 수 있다.The entrance and exit portion 12 is compressed from the outside to the inside of the pair of pin members (11a, 11b) to adjust the micro-gap of the entry and exit portion 12, the receiving portion 13 to the impregnation amount of the DNA sample Therefore, it can be produced in various forms, such as straight, streamlined.
따라서, DNA 시료는 한쌍의 핀부재(11a, 11b)에 의해 형성되는 입출부(12)를 통해 인입되고, 상기 입출부(12)를 통해 인입되는 DNA 시료는 일정 곡률 반경을 가지는 수용부(13)에 용적된다.Therefore, the DNA sample is introduced through the entry and exit 12 formed by the pair of pin members 11a and 11b, and the DNA sample introduced through the entry and exit 12 is a receiving portion 13 having a predetermined radius of curvature. Volume).
이후, DNA 시료가 용적되어 있는 DNA 함침 핀을 이동시켜 유리판 또는 나이론 멤블레이너 상에 찍으면 상기 DNA 함침 핀에 용적되어 있는 DNA시료가 유출되어 스팟을 형성한다.Subsequently, when the DNA impregnated pin, in which the DNA sample is deposited, is moved and taken on a glass plate or a nylon membrane, the DNA sample deposited on the DNA impregnated pin flows out to form a spot.
그러나, 상기와 같이 종래의 DNA 함침 핀은 한 쌍의 핀부재(11a, 11b)를 압축하여 입출부(12)의 간격을 조절하므로 입출부(12)의 간격을 미세하게 조절할 수 없어 정밀도가 낮아진다는 문제점이 있다.However, as described above, the conventional DNA impregnating pin compresses a pair of pin members 11a and 11b to adjust the gap between the entry and exit portions 12, so that the gap between the entry and exit portions 12 cannot be finely adjusted and thus the precision is low. Has a problem.
또한, 상기 입출부(12)의 간격을 조절하기 위해 한 쌍의 핀부재(11a, 11b)를 압축하므로 높은 경도을 가지는 금속 소재를 사용할 수 없어 DNA 함침 핀의 내마모성이 떨어진다는 문제점이 있다.In addition, since the pair of pin members 11a and 11b are compressed to adjust the gap between the entry and exit portions 12, a metal material having a high hardness cannot be used, and thus, the wear resistance of the DNA impregnation pin is inferior.
본 발명은 전술한 바와 같은 문제점을 감안하여 안출한 것으로, 그 목적 DNA 시료를 용적할 수 있는 DNA 함침 핀의 간격을 미세하게 조절할 수 있게 함으로써 DNA 함침 핀의 정밀도를 향상시키기 위한 것이다.The present invention has been made in view of the above-described problems, and is intended to improve the precision of DNA impregnated pins by making it possible to finely adjust the interval of the DNA impregnated pins, which can volume the target DNA sample.
또 다른 목적은 내구성이 강한 소재를 사용할 수 있게 함으로써 DNA 함침 핀의 반복적인 사용으로 인한 표면의 변형 및 형태 변화를 최소화 시키기 위한 것이다.Another aim is to minimize surface deformation and morphological changes due to the repeated use of DNA impregnated pins by enabling the use of durable materials.
도 1는 종래의 DNA 함침 핀을 도시한 사시도이다.1 is a perspective view showing a conventional DNA impregnation pin.
도 2는 본 발명의 DNA 함침 핀을 도시한 분해 사시도이다.Figure 2 is an exploded perspective view showing the DNA impregnation pin of the present invention.
도 3은 본 발명의 DNA 함침 핀을 도시한 조립도이다.도 4는 본 발명의 DNA 함침 핀의 정면도이다.Fig. 3 is an assembly view showing the DNA impregnation pin of the present invention. Fig. 4 is a front view of the DNA impregnation pin of the present invention.
*도면의 주요 부분에 대한 부호의 설명** Description of the symbols for the main parts of the drawings *
11a, 11b : 핀부재 12 : 입출부11a, 11b: pin member 12: entry and exit portion
13, 50 : 수용부 20 : 몸체13, 50: receiving portion 20: body
21 : 제 1접착면 23 : 제 1굴곡면21: first adhesive surface 23: the first curved surface
25 : 제 1평탄면 30 : 핀부재25: first flat surface 30: pin member
31 : 제 2접착면 33 : 제 2굴곡면31: second bonding surface 33: second bending surface
35 : 제 2평탄면 40 : 미세간격35: second flat surface 40: fine spacing
상기의 목적을 달성하기 위한 본 발명의 DNA 함침 핀의 제조방법은 다음과 같이 구성되어 있다.Method for producing a DNA impregnated pin of the present invention for achieving the above object is configured as follows.
용접에 의해 접착되는 제 1접착면과, 상기 제 1접착면과 일정 곡률반경으로굴곡되어 DNA 시료를 용적하는 제 1굴곡면과, 상기 제 1굴곡면과 일정 곡률반경으로 굴곡되어 DNA 함침 핀의 가장자리에 일정한 간격을 유지하는 제 1평탄면을 형성하는 몸체와, 상기 몸체에 면 대향되게 제 2접착면, 제 2굴곡면, 제 2평탄면을 형성하는 핀부재를 분리하여 가공하는 가공공정과,The first adhesive surface bonded by welding, the first curved surface and the first curved surface is bent to a predetermined radius of curvature to the volume of the DNA sample, and the first curved surface is bent to the constant radius of curvature and the DNA impregnation pin A processing step of separating and processing a body forming a first flat surface having a constant spacing at an edge, and a pin member forming a second adhesive surface, a second curved surface, and a second flat surface so as to face the body; ,
상기 제 1평탄면과 제 2평탄면 사이에는 미세간격이 이격되어 형성되고, 한 쌍의 제 1굴곡면과 제 2굴곡면에는 DNA 시료를 용적할 수 있는 수용부가 형성되도록 핀부재의 제 2접착면을 몸체의 제 1접착면에 밀착시켜 조립하는 조립공정과,A second gap is formed between the first flat surface and the second flat surface so as to be spaced apart from each other, and the pair of first curved surfaces and the second curved surfaces are provided with an accommodating portion capable of depositing a DNA sample. An assembling process of assembling the surface by bringing it into close contact with the first adhesive surface of the body;
상호 밀착되어 있는 제 1접착면과 제 2접착면이 고정될 수 있도록 용접하는 용접공정으로 이루어지는 것을 특징으로 한다.Characterized in that the welding process for welding so that the first adhesive surface and the second adhesive surface which are in close contact with each other can be fixed.
이하, 첨부된 도면을 참고로 하여 본 발명의 바람직한 실시예를 상세히 설명하면 다음과 같다.Hereinafter, exemplary embodiments of the present invention will be described in detail with reference to the accompanying drawings.
도 2는 본 발명의 DNA 함침 핀을 도시한 분해 사시도 이다.Figure 2 is an exploded perspective view showing a DNA impregnation pin of the present invention.
도 3은 본 발명의 DNA 함침 핀을 도시한 조립도이다.도 4는 본 발명의 DNA 함침 핀의 정면도이다.Fig. 3 is an assembly view showing the DNA impregnation pin of the present invention. Fig. 4 is a front view of the DNA impregnation pin of the present invention.
도 2 내지 도 3를 참조하면, 본 발명의 DNA 함침 핀의 제조방법은 DNA 시료를 용적할 수 있도록 몸체(20)와 상기 몸체(20)에 용접되는 핀부재(30)를 분리하여 가공하는 가공공정과, 상기 가공공정에서 가공된 몸체(10)와 핀부재(30)를 조립하는 조립공정과, 상기 조립공정에서 조립된 몸체(20)와 핀부재(30)를 용접하는 용접공정으로 이루어져 있다.2 to 3, the method of manufacturing the DNA impregnated pin of the present invention is processed to separate the body 20 and the pin member 30 welded to the body 20 so that the DNA sample volume Process, and an assembly process of assembling the body 10 and the pin member 30 processed in the processing process, and a welding process of welding the body 20 and the pin member 30 assembled in the assembly process. .
상기 가공공정에서 가공되는 몸체(20)에는 용접에 의해 접착되는 제 1접착면(21)과, 상기 제 1접착면(21)과 일정 곡률반경으로 굴곡되어 DNA 시료를 용적하는 제 1굴곡면(23)과, 상기 제 1굴곡면(23)과 일정 곡률반경으로 굴곡되어 DNA 함침 핀의 가장자리에 일정한 간격을 형성시키는 제 1평탄면(25)이 형성되며, 상기 핀부재(30)에는 상기 몸체(20)에 형성되어 있는 제 1접착면(21), 제 1굴곡면(23), 제 1평탄면(25)과 서로 면 대향되게 제 2접착면(31), 제 2굴곡면(33), 제 2평탄면(35)이 형성되어 있다.The body 20 to be processed in the processing step is a first adhesive surface 21 which is bonded by welding, the first bending surface and the first bending surface to be bent at a predetermined radius of curvature with the first adhesive surface 21 ( 23) and a first flat surface 25 that is bent at a predetermined curvature radius with the first curved surface 23 to form a predetermined gap at the edge of the DNA impregnated pin is formed, the pin member 30 is the body The first adhesive surface 21, the first curved surface 23, and the first flat surface 25 formed on the surface 20 of the second adhesive surface 31 and the second curved surface 33 to face each other. The second flat surface 35 is formed.
상기 조립공정은 상기 핀부재(30)를 몸체(20)에 접촉시키면, 한 쌍의 제 1접착면(21)과 제 2접착면(31)이 밀착되고, 한 쌍의 제 1굴곡면(33)과 제 2굴곡면(33)이 DNA 시료를 용적할 수 있도록 합치되며, 제 1평탄면(25)과 제 2평탄면(35) 사이에는 미세간격이 형성되도록 면 대향되게 조립된다.In the assembling process, when the pin member 30 is brought into contact with the body 20, the pair of first adhesive surfaces 21 and the second adhesive surface 31 are in close contact with each other, and the pair of first curved surfaces 33 are in contact with each other. ) And the second curved surface 33 are matched to the volume of the DNA sample, and are assembled so as to face each other so that a minute gap is formed between the first flat surface 25 and the second flat surface 35.
용접공정은 상호 접촉되어 있는 몸체(20)와 핀 부재(30)의 제 1접착면(21)과 제 2접착면(31)이 고정될 수 있도록 용접한다.The welding process welds the first adhesive surface 21 and the second adhesive surface 31 of the body 20 and the pin member 30 which are in contact with each other to be fixed.
따라서, 상기에서와 같이 가공되어진 DNA 함침 핀의 몸체(20)와 핀부재(30)를 서로 면대항 되게 조립하여 용접하면 DNA 함침 핀의 가장자리에 상기 제 1평탄면(25)과 제 2평탄면(35)이 일정 간격만큼 이격됨에 따라, 미세간격(40)이 형성되고, 이 미세간격(40)을 통해 DNA 시료가 입출되며, 상기 미세간격을 통해 인입된 DNA 시료를 용적할 수 있는 수용구(50)가 제 1굴곡면(23)과 제 2굴곡면(33)에 의해 일정 공간으로 형성된다.Therefore, when the body 20 and the pin member 30 of the DNA impregnated pin processed as described above are assembled to face each other and welded, the first flat surface 25 and the second flat surface at the edge of the DNA impregnated pin. As the 35 is spaced by a predetermined interval, the micro-gap 40 is formed, the DNA sample is extracted through the micro-gap 40, the receiving port that can volume the DNA sample introduced through the micro-gap. 50 is formed in a predetermined space by the first curved surface 23 and the second curved surface 33.
상기 미세간격(40)은 1/100[mm], 오차범위는 ±3/1000~1/1000로 형성하는 것이 바람직하며, 상기 수용구(50)의 형태는 용적량에 따라 다양하게 형성할 수 있다.The fine interval 40 is preferably 1/100 [mm], the error range is ± 3/1000 ~ 1/1000, the shape of the receiving port 50 can be formed in various ways depending on the volume. .
이상에서 설명한 바와 같은 본 발명의 작용 및 효과를 살펴보면 다음과 같다.Looking at the operation and effects of the present invention as described above are as follows.
용접에 의해 접착되는 제 1접착면(21)과, 상기 제 1접착면(21)과 일정 곡률반경으로 굴곡되어 DNA 시료를 용적하는 제 1굴곡면(23)과, 상기 제 1굴곡면(23)과 일정 곡률반경으로 굴곡되어 DNA 함침 핀의 가장자리에 일정한 간격을 유지하는 제 1평탄면(25)을 형성하는 몸체(20)와, 상기 몸체(20)에 면 대향되게 제 2접착면(21), 제 2굴곡면(33), 제 2평탄면(35)을 형성하는 핀부재(30)를 별도로 분리하여 가공한다.A first adhesive surface 21 adhered by welding, a first curved surface 23 that is bent to a predetermined radius of curvature with the first adhesive surface 21, and a first curved surface 23 for depositing a DNA sample, and the first curved surface 23 ) And a body 20 to be bent at a constant radius of curvature to form a first flat surface 25 that maintains a constant distance to the edge of the DNA impregnation pin, and the second adhesive surface 21 to face the body 20. ), The second curved surface 33, and the pin member 30 forming the second flat surface 35 is separated and processed.
따라서, DNA 함침 핀을 제조하기 위해 몸체(20)와 핀부재(30)로 분리하여 가공함으로써 초경 합금등과 같은 내구성이 우수한 금속소재를 사용하여 DNA 함침 핀을 제작할 수 있다.Therefore, the DNA impregnation pin can be manufactured using a metal material having excellent durability, such as cemented carbide, by separating and processing the body 20 and the pin member 30 to manufacture the DNA impregnation pin.
이후, 상기 제 1평탄면(25)과 제 2평탄면(35) 사이에 미세간격(40)이 형성되고, 한 쌍의 제 1굴곡면(23)과 제 2굴곡면(33)이 DNA 시료를 용적할 수 있는 수납구(40)가 형성되도록 핀부재(30)의 제 2접착면(31)을 몸체(20)의 제 1접착면(21)에 밀착시켜 조립한 다음, 상기 제 1접착면(21)과 제 2접착면(31)을 용접하여 DNA 함침 핀을 제작한다.Thereafter, a fine gap 40 is formed between the first flat surface 25 and the second flat surface 35, and the pair of first curved surfaces 23 and the second curved surfaces 33 are DNA samples. The second adhesive surface 31 of the pin member 30 is assembled to the first adhesive surface 21 of the body 20 so as to form a receiving opening 40 capable of forming a volume, and then the first adhesive surface is assembled. (21) and the second adhesive surface 31 are welded to produce a DNA impregnation pin.
따라서, 상기 제 1평탄면(25)과 제 2평탄면(35) 사이에 형성되는 미세간격(40)을 상기 핀부재(30)의 이동에 따라 미세하게 조절할 수 있으므로 상기 DNA 함침 핀에 미세간격(40)을 정밀하게 형성할 수 있다.Therefore, the micro-gap 40 formed between the first flat surface 25 and the second flat surface 35 can be finely adjusted according to the movement of the pin member 30, so that the micro-interval on the DNA impregnated pin 40 can be formed precisely.
이상에서 설명한 바와 같이 본 발명은 몸체와 핀부재로 분리하여 DNA 함침 핀을 제작함으로써 내구성이 우수한 금속 소재를 사용할 수 있으며, 내구성이 우수한 금속 소재를 사용함으로써 DNA 함침 핀의 반복적인 사용으로 인한 표면의 변형이나 형태변화를 감소시킨다.As described above, the present invention can use a metal material having high durability by separating the body and the pin member to produce a DNA impregnation pin, and by using a metal material having high durability, Reduces deformation or shape change
또한, DNA 함침 핀의 가장자리에 형성되는 미세간격을 몸체에 조립되는 핀부재를 이용하여 미세하게 조절할 수 있으므로 DNA 함침 핀의 정밀도를 향상시킨다.In addition, the fine spacing formed at the edge of the DNA impregnation pin can be finely adjusted using a pin member assembled to the body, thereby improving the precision of the DNA impregnation pin.
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US5807522A (en) * | 1994-06-17 | 1998-09-15 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for fabricating microarrays of biological samples |
US6101946A (en) * | 1997-11-21 | 2000-08-15 | Telechem International Inc. | Microarray printing device including printing pins with flat tips and exterior channel and method of manufacture |
JP2001215233A (en) * | 2000-02-03 | 2001-08-10 | Mitsubishi Chemicals Corp | Spotting pin |
KR20020085495A (en) * | 2001-05-08 | 2002-11-16 | (주)바이오니아 | Spotting Pin for microarraying of biological preparation |
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US5807522A (en) * | 1994-06-17 | 1998-09-15 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for fabricating microarrays of biological samples |
US6101946A (en) * | 1997-11-21 | 2000-08-15 | Telechem International Inc. | Microarray printing device including printing pins with flat tips and exterior channel and method of manufacture |
JP2001215233A (en) * | 2000-02-03 | 2001-08-10 | Mitsubishi Chemicals Corp | Spotting pin |
KR20020085495A (en) * | 2001-05-08 | 2002-11-16 | (주)바이오니아 | Spotting Pin for microarraying of biological preparation |
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