Method for reducing contact resistance of crystalline silicon solar cell

The invention discloses a method for reducing the contact resistance of a crystalline silicon solar cell, and the method comprises the steps: enabling each conductive wire which is arranged in parallel to be correspondingly pressed on a main grid line of a surface electrode of the solar cell, and enabling the conductive wires to extend in the extension direction of the main grid lines; electrically connecting the first end of a power supply with each conductive wire, electrically connecting the second end of the power supply with the back electrode of the solar cell, and applying reverse voltage to the solar cell through the power supply; a strip-shaped laser spot is irradiated on the solar cell, and the strip-shaped laser spot extends along a second direction; the strip-shaped laser spot moves in the extension direction of the main grid line to scan a surface electrode of the solar cell, and atoms of the metal and semiconductor materials are remelted and recrystallized at an interface; ...

一段人型乳头瘤病毒-6 DNA序列（1）特异性的确定及其应用

The present invention relates to definition of specificity of a tract of human papillomavirus-6 DNA sequence (1) and its application, belonging to the field of biomedicine technology. It utilizes the search and analysis of the gene data base material to define the specificity of a tract of human papillomavirus-6 DNA sequence (1) and PCR amplification primer, the length of said sequence is 213 bp. It utilizes the PCR amplification and clone of the human genital duct human papillomavirus-6 infection specimen to obtain said sequence, and the sequencing shows that sequence is identical to the predefined sequence, and the results of biological information method analysis and gene chip hybridization analysis show the specificity of said sequence. Said invention can be used as probe of gene chip diagnosis and PCR amplification detection sequence for diagnosing human papillomavirus-6.

一段脲解支原体DNA序列（5）特异性的确定及其应用

A determination to the specificity of a urea-decomposing mycoplasma DNA sequence (5) segment includes searching and analyzing gene database to determine the specificity of said DNA sequence (288 bp) segment and its PCR amplification primer, PCR amplificating and cloning to human genetic tract's urea-decomposing mycoplasma infective specimen to obtain the sequence, sequencing it to prove that it is consistant with the predicated sequence, biological information analysis, and gene chip cross analysis to prove the specificity of said sequence to urea-decomposing mycoplasma. It can be used as the probe of gene chip diagnosis and the test sequence of PCR amplification to diagnose human mycoplasma.

一段阴道加德纳氏杆菌DNA序列（5）特异性的确定及其应用

The present invention utilizes the search of the gene data base material and analysis of them to define the specificity of a tract of vaginal Gardner's bacillus DNA sequence (5) and PCR amplification primer, and the length of said sequence is 205 bp. Said invention utilizes the PCR amplification and clone of woman vaginal Gardner's bacillus infection specimen to obtain said sequence, and the sequencing shows that said sequence is identical to the predefined sequence, and the results of biological information method analysis and gene chip hybridization analysis show the specificity of said sequence. Said invention can be used as probe of gene chip diagnosis and PCR amplification detection sequence for diagnosing vaginal Gardner's bacillus.

一段脲解支原体DNA序列(1)特异性的确定及其应用

The present invention utilizes the search and analysis of gene data base to define the specificity of a segmentum of urea-hydrolyzed mycoplasma DNa sequence (1) and PCR amplification primer, said sequence length is 215 bp. Said sequence can be obtained by PCR amplification and clone of human genital tract urea-hydrolyzed mycoplasma infection specimen. Said invention can be used as probe for gene chip diagnosis and PCR amplification detection sequence for diagnosis of urea-hydrolyzed mycoplasma.

一段白色念珠菌DNA序列（2）特异性的确定及其应用

The present invention utilizes the search and analysis of gene data base to define the specificity of a segmentum of Candida albicans DNA sequence (2) and PCR amplification primer. Said sequence length is 184 bp, and said sequence can be obtained by means of PCR amplification and clone of female genital tract candida albicans infection specimen. Said invention can be used as probe for gene chip diagnosis and PCR amplification detection sequence for accurately diagnosing candida albicans infection.

一段人型支原体DNA序列（4）特异性的确定及其应用

The present invention relates to determination of a section of man-shaped mycoplasma DNA sequence (4) specificity and its application, and belongs to the field of biotechnology. Via search and analysis of gene data base information, one section of man-shaped mycoplasma DNA sequence (4) specificity and PCR amplimer are determined, with the sequence length being 202 bp. The sequence is obtained through the amplification and cloning of human genital tract man-shaped mycoplasma infection specimen, and its specificity to man-shaped mycoplasma is proved through bioinformatic analysis and gene chip hybridizing analysis. The present invention is used as the probe for gene chip diagnosis and PCR amplification detecting sequence in diagnosing man-shaped mycoplasma. The clinical detection technological method has the advantages of being fast, accurate, simple in operation and low in cost.

一段人型支原体DNA序列（5）特异性的确定及其应用

The present invention relates to determination of a section of man-shaped mycoplasma DNA sequence (5) specificity and its application, and belongs to the field of biotechnology. Via search and analysis of gene data base information, one section of man-shaped mycoplasma DNA sequence (5) specificity and PCR amplimer are determined, with the sequence length being 219 bp. The sequence is obtained through the amplification and cloning of human genital tract man-shaped mycoplasma infection specimen, and its specificity to man-shaped mycoplasma is proved through bioinformatic analysis and gene chip hybridizing analysis. The present invention is used as the probe for gene chip diagnosis and PCR amplification detecting sequence in diagnosing man-shaped mycoplasma. The clinical detection technological method has the advantages of being fast, accurate, simple in operation and low in cost.

一段淋球菌DNA序列（5）特异性的确定及其应用

The present invention utilizes the search and analysis of gene data base to define the specicity of a segmentum of gonococcus DNA sequence (5) and PCR amplification primer, sand sequence length is 187 bp, and said sequence can be obtained by PCR amplification and clone of human genital tract gonococcus infection specimen. Said invention can be used as probe for gene chip diagnosis and PCR amplification detection sequence for diagnosis of gonococcus infection.

Human type mycoplasma DNA sequence (3) specificity determination and its uses

The invention relates to the determination and the use for the specificity of a section of mycoplasma hominis DNA sequence (3), which belongs to the field of the biomedicine technology. The specificity and the PCR amplimer of a section of mycoplasma hominis DNA sequence (3) are determined by searching and analyzing the data in the gene database, and the length of the sequence is 222bp. The sequence is obtained by PCR amplification and cloning of the mycoplasma hominis infected specimen in human genital tract, and the determined sequence is coincident with the predicted sequence. The specificity of the sequence to the mycoplasma hominis is defined by biological informatics method and gene chip hybridization analysis.

一段人型乳头瘤病毒-6 DNA序列（4）特异性的确定及其应用

The present invention relates to definition of specificity of a tract of human papillomavirus-6 DNA sequence (4) and its application, belonging to the field of biomedicine technology. It utilizes the search and analysis of the gene data base material to define the specificity of a tract of human papillomavirus-6 DNA sequence (4) and PCR amplification primer, and the length of said sequence is 203 bp. It utilizes the PCR amplification and clone of human genital duct human papillomavirus-6 infection specimen to obtain said sequence, and the sequencing shows that said sequence is identical to the predefined sequence, and the results of biological information method analysis and gene chipp hybridization analysis show the specificity of said sequence. Said invention can be used as probe of gene chip diagnosis and PCR amplification detection sequence for diagnosing human papillomavirus-6.

Determination of man-shaped mycoplasma DNA sequence (5) specificity and its use

Specificity determination and application of one section of gonococcus DNA sequence

The present invention relates to specificity determination and application of one section of gonococcus DNA sequence, and belongs to the field of biomedicine. Through gene data base data search and analysis, the specificity and PCR amplification primer of one section of gonococcus DNA sequence is determined, and the sequence length is 197 bp. By means of PCR amplification and cloning of human genital tract gonococcus infection sample, the sequence is obtained and sequenced to obtain the result the same as the predicted. Biological informatics and gene chip hybrid analysis proves the specificity of the sequence to gonococcus. The present invention is used as probe and PCR amplification detection squence for gene chip diagnosis for gonococcus.

Multifunctional airtight detector and detection method thereof

The invention discloses a multifunctional airtight detector and a detection method thereof, and belongs to the leakage measuring technical field; the multifunctional airtight detector comprises a compressed gas path, a tracer gas path, a gas outlet valve, a communication valve, a standard component gas path, a to-be tested piece gas path, a static pressure sensor, a differential pressure transmitter and a gas detection gas path; the compressed gas path comprises a compressed gas pressure-reducing valve and a compressed gas inlet valve in sequence; the tracer gas path comprises a tracer gas pressure-reducing valve and a tracer gas inlet valve in sequence; the standard component gas path comprises a standard component sub-valve and a standard component; the to-be tested piece gas path comprises a to-be tested piece sub-valve and a to-be tested piece; the gas detection gas path comprises a probe, a laser detector and a gas collection pump in sequence; the beneficial effects are that the detection ...

一段人型支原体DNA序列（1）特异性的确定及其应用

A determination to the specificity of a human mycoplasma DNA sequence (1) segment includes searching and analyzing the gene database to determine the specificity of a human mycoplasma DNA sequence (196 bp) and its PCR amplification primer, PCR amplificating and cloning to human genetic tract's human mycoplasma infectious specimen to obtain the sequence, sequencing it to prove that it is consistent with the predicted sequence, biological information analyzing and gene chip cross analyzing to prove its specificity to human mycoplasma. It can be used as the probe of gene chip diagnosis and the test sequence of PCR amplification to diagnose human mycoplasma.

一段白色念珠菌DNA序列（4）特异性的确定及其应用

The present invention utilizes the search and analysis of gene bata base to define the specificity of a segmentum of Candida albicans DNA sequence (4) and PCR amplification primer, and said sequence length is 202bp. Said sequence is obtained by PCR amplification and clone of female genital tract candida albicans infection specimen. Said invention can be used as probe for gene chip diagnosis and PCR amplification detection sequence for diagnosis of Candida albicans.

一段人型乳头瘤病毒-6 DNA序列（2）特异性的确定及其应用

The present invention relates to definition of specificity of a tract of human papillomavirus-6 DNA sequence (2) and its application, belonging to the field of biomedicine technology. It utilizes the search and analysis of the gene data base material to define the specificity of a tract of human papillomavirus-6 DNa sequence (2) and PCR amplification primer, and the length of said sequence is 189 bp. It utilizes the PCR amplification and clone of the human genital duct human papillomavirus-6 infection specimen to obtain said sequence, and the sequencing shows that the sequence is identical to the predefined sequence, and the results of biological information method analysis and gene chip hybridization analysis show the specificity of said sequence. Said invention can be used as probe of gene chip diagnosis and PCR amplification detection sequence for diagnosing human papillomavirus-6.

一段白色念珠菌特异性DNA序列（4）的确定及其应用

... 本发明涉及一段白色念珠菌特异性DNA序列(4)的确定及其应用，属于生物医学技术领域。本发明通过基因数据库资料的搜寻和分析，确定了一段白色念珠菌DNA序列的特异性及PCR扩增引物，该序列长度为202bp。通过对妇女生殖道白色念珠菌感染标本的PCR扩增，克隆，获得该序列，测序证明与预计序列一致。再经生物信息学方法分析，基因芯片杂交分析，结果证实了该序列对于白色念珠菌的特异性。本发明作为基因芯片诊断的探针及PCR扩增检测序列，用于白色念珠菌的诊断。用本发明建立的临床检测技术所使用的方法具有快速、准确、操作简便、成本低等优点。 ...

一段白色念珠菌特异性DNA序列（5）的确定及其应用

... 本发明涉及一段白色念珠菌特异性DNA序列(5)的确定及其应用，属于生物医学技术领域。本发明通过基因数据库资料的搜寻和分析，确定了一段白色念珠菌DNA序列(5)的特异性及PCR扩增引物，该序列长度为192bp。通过对妇女生殖道白色念珠菌感染标本的PCR扩增，克隆，获得该序列，测序证明与预计序列一致。再经生物信息学方法分析，基因芯片杂交分析，结果证实了该序列对于白色念珠菌的特异性。用本发明建立的临床检测技术所使用的方法具有快速、准确、操作简便、成本低等优点。 ...

Specificity determination and application of one section of candida albicans DNA sequence

The present invention relates to specificity determination and application of one section of candida albicans DNA sequence, and belongs to the field of biomedicine. Through gene data base data searchand analysis, the specificity and PCR amplification primer of one section of candida albicans DNA sequence is determined, and the sequence length is 241 bp. By means of PCR amplification and cloning of women's genital tract candida albicans infection sample, the sequence is obtained and sequenced to obtain the result the same as the predicted. Biological informatics and gene chip hybrid analysis proves the specificity of the sequence to candida albicans. The present invention is used as probe and PCR amplification detection sequence for gene chip diagnosis for candida albicans.

一段人型支原体DNA序列（2）特异性的确定及其应用

The present invention relates to determination of a section of man-shaped mycoplasma DNA sequence (2) specificity and its application, and belongs to the field of biotechnology. Via search and analysis of gene data base information, one section of man-shaped mycoplasma DNA sequence (2) specificity and PCR amplimer are determined, with the sequence length being 221 bp. The sequence is obtained through the amplification and cloning of human genital tract man-shaped mycoplasma infection specimen, and its specificity to man-shaped mycoplasma is proved through bioinformatic analysis and gene chip hybridizing analysis. The present invention is used as the probe for gene chip diagnosis and PCR amplification detecting sequence in diagnosing man-shaped mycoplasma. The clinical detection technological method has the advantages of being fast, accurate, simple in operation and low in cost.

一段阴道加德纳氏杆菌DNA序列（4）特异性的确定及其应用

The present invention relates to definition of specificity of a tract of vaginal Gardner's bacillus DNA sequence (4) and its application, belonging to the field of biomedicine technology. It utilizes the search and analysis of the gene data base material to define the specificity of a tract of vaginal Gardner's bacillus DNA sequence (4) and PCR amplification primer, and the length of said sequence is 190 bp. It utilizes the PCR amplification and clone of woman vaginal Gardner's bacillus infection specimen to obtain said sequence, and the sequencing shows that said sequence is identical to the predefined sequence, and the results of biological informatic method analysis and gene chip hybridization analysis show the specificity of said sequence. Said invention can be used as probe of gene chip diagnosis and PCR amplification detection sequence for diagnosing vaginal Gardner's bacillus.

一段白色念珠菌特异性DNA序列（2）的确定及其应用

... 本发明涉及一段白色念珠菌特异性DNA序列(2)的确定及其应用，属于生物医学技术领域。本发明通过基因数据库资料的搜寻和分析，确定了一段白色念珠菌DNA序列(2)的特异性及PCR扩增引物，该序列长度为184bp。通过对妇女生殖道白色念珠菌感染标本的PCR扩增，克隆，获得该序列，测序证明与预计序列一致。再经生物信息学方法分析，基因芯片杂交分析，结果证实了该序列对于白色念珠菌的特异性。本发明作为基因芯片诊断的探针及PCR扩增检测序列，用于白色念珠菌的诊断。用本发明建立的临床检测技术所使用的方法具有快速、准确、操作简便、成本低等优点。 ...

一段白色念珠菌DNA序列（5）特异性的确定及其应用

The present invention utilizes the search and analysis of gene data base to define specificity of a segmentum of Candida albicans DNA sequence (5) and PCR amplification primer, and said sequence length is 192 bp. Said sequence can be obtained by PCR amplification and clone of female genital tract candida albican infection specimen. Said invention utilizes the biological informatics method analysis and gene chip hybridization analysis to define the specificity of said sequence to candida albicans, and can be used as a quick and accurate clinical detection method for candida albicans infection.

一段白色念珠菌特异性DNA序列（3）的确定及其应用

... 本发明涉及一段白色念珠菌特异性DNA序列(3)的确定及其应用，属于生物医学技术领域。本发明通过基因数据库资料的搜寻和分析，确定了一段白色念珠菌DNA序列(3)的特异性及PCR扩增引物，该序列长度为192bp。通过对妇女生殖道白色念珠菌感染标本的PCR扩增，克隆，获得该序列，测序证明与预计序列一致。再经生物信息学方法分析，基因芯片杂交分析，结果证实了该序列对于白色念珠菌的特异性。本发明作为基因芯片诊断的探针及PCR扩增检测序列，用于白色念珠菌的诊断用本发明建立的临床检测技术所使用的方法具有快速、准确、操作简便、成本低等优点。 ...

一段淋球菌DNA序列（3）特异性的确定及其应用

The present invention utilizes the search and analysis of gene data base to define the specicity of a segmentum of gonococcus DNA sequence (3) and PCR amplification primer, said sequence length is 190 bp, and said sequence can be obtained by PCR amplification and clone of human genital tract gonococcus infection specimen. Said invention can be used as probe for gene chip diagnosis and PCR amplification detection sequence for quick and accurate diagnosis of gonococcus infection.

一段白色念珠菌DNA序列（3）特异性的确定及其应用

The present invention utilizes the search and analysis of gene data base to define the specificity of a segmentum of Candida albicans DNA sequence (3) and PCR amplification primer, and said sequence length is 192 bp. Said sequence can be obtained by PCR amplification and clone of female genital tract candida albicans infection specimen. Said invention can be used as probe for gene chip diagnosis and PCR amplification detection sequence for accurately clinical diagnosis of candida albicans infection.

一段人型乳头瘤病毒-6 DNA序列（3）特异性的确定及其应用

The present invention relates to definition of specificity of a tract of human papillomavirus-6 DNA sequence (3) and its application, belonging to the field of biomedicine technology. It utilzies the search and analysis of the gene data base material to define the specificity of a tract of human papillomavirus-6 DNA sequence (3) and PCR amplification primer, and the length of said sequence is 198 bp. It utilizes the PCR amplification and clone of the human genital duct human papillomavirus-6 infution specimen to obtain said sequence, and the sequencing shows that said sequence is identical to the predefined sequence, and the results of biological informatic method analysis and gene chip hybridization analysis show the specificity of said sequence. Said invention can be used as probe of gene chip diagnosis and PCR amplification detection sequence for diagnosing human papillomavirus-6.

Determination of man-shaped mycoplasma DNA sequence (2) specificity and its use

Quadruplex position airtightness detector

The utility model discloses a quadruplex position airtightness detector relates to the measurement field of leaking, including central controller and four group control valves, including display system, microcomputer control system, pressure detection system and air pressure system in the central controller, the microcomputer control system respectively with display system, pressure detection system and gas circuit system electric connection, pressure detection system and gas circuit system electric connection, the air pressure system is connected with the four group's workpieces for measurement through four group control valves, the beneficial effects of the utility model are that simple structure, the easy manufacturing, it is with low costs, for the customer improves product detection efficiency, create better benefit.

一段阴道加德纳氏杆菌DNA序列（1）特异性的确定及其应用

The present invention relates to the definition of specificity of a tract of vaginal Gardner's bacillus DNA sequence (I) and its application. It utilizes the search and analysis of gene data base material to define the specificity of at tract of vaginal Gardern's bacillus DNA sequence (I) and PCR amplification primer, and the length of said sequence is 200bp. It utilizes the PCR amplification and clone of woman vaginal Gardner's bacillus infection specimen to obtain said sequence. The sequencing shows that said sequence is identical to the predefined sequence, and the results of biological informatic method analysis and gene chip hybridization analysis show the specificity of said sequence. Said invention can be used as probe of gene chip diagnosis and PCR amplification detection sequence for diagnosing vaginal Gardner's bacillus.

一段阴道加德纳氏杆菌DNA序列（3）特异性的确定及其应用

The specificity and PCR amplification primer of a viginal Gardener's bacillus DNA sequence (3) fragment are determined by searching and analyzing the data of gene database. Said sequence with 196 bp in length is obtained by PCR amplification and clone of said viginal Gardener's bacillus infected specimen. It can be used to diagnose the viginal Gardener's bacillus with high speed and correctness and low cost.

一段淋球菌DNA序列（4）特异性的确定及其应用

The present invention utilizes the search and analysis of gene data base to define the specificity of a segmentum of gonococcus DNA sequence (4) and PCR amplification primer, said sequence length is 212 bp. and said sequence can be obtained by PCR amplification and clone of human genital tract gonococcus infection specimen. Said invention can be used as probe for gene chip diagnosis and PCR amplification detection sequence for accurately diagnosing gonococeus infection.

Determination of a section of mycoplasma urealyticum DNA sequence (4) specificity and its use

Preparation method of silicon adapter plate with multi-layer cross wiring structure

The invention relates to a preparation method of a silicon adapter plate with a multi-layer cross structure. The preparation method comprises the following steps of: manufacturing large-scale metal wires on the surface of a silicon substrate step by step and arranging salient points of the metal wires; the selected dielectric layers such as a silicon dioxide layer and a silicon nitride, photosensitive polyimide adhesive, BCB adhesive and the like are used as insulating dielectric layers of metal wires distributed among different layers in an insulating manner; due to the alternate layout of the metal layer wiring and the dielectric layer, a large number of metal wires can be distributed, more salient points can be distributed and arranged, multi-layer staggered interconnection is formed, and the salient points are located on the same horizontal plane; according to the method, the silicon adapter plates with different film layers are prepared on the surface of the silicon wafer, so that ...

一段人型乳头瘤病毒-6 DNA序列（5）特异性的确定及其应用

The present invention relates to the definition of specificity of a tract of human papillomavirus-6 DNA sequence (5) and its application. It utilizes the search and analysis of gene data base material to define the specificity of a tract of human papillomavirus-6 DNA sequence (5) and PCR amplification primer, and the length of said sequence is 214 bp. It utilizes the PCR amplification and clone of human genital duct human papillomavirus-6 infection specimen to obtain said sequence, and the sequencing shows that the sequence is identical to the predefined sequence, and the results of the biological informatic method analysis and gene chip hybridization analysis show the specificity of said sequence. Said invention can be used as probe of gene chip diagnosis and PCR amplification detection sequence for diagnosing human papillomavirus-6.

Determination of specificity for a segment of ureaplasma DNA sequence and use thereof

The invention relates to a segment of urea decomposed mycoplasma DNA sequence specificity determination and use thereof, wherein gene data bank searching and analysis is conducted, the sequence length is 294bp, the specificity of the sequence to urea decomposed mycoplasma is confirmed.

一段阴道加德纳氏杆菌DNA序列（2）特异性的确定及其应用

The specificity and PCR amplification primer of a viginal Gardener's bacillus DNA sequence (2) fragment are determined by searching and analyzing the data of gene database. Said sequence with 209 bp in length is obtained by PCR amplification and clone of said viginal Gardener's bacillus infected specimen. It can be used to diagnose the viginal Gardener's bacillus with high speed and correctness and low cost.

一段脲解支原体特异性DNA序列(1)的确定及其应用

... 本发明涉及一段脲解支原体特异性DNA序列(1)的确定及其应用，属于生物医学技术领域。本发明通过基因数据库资料的搜寻和分析，确定了一段脲解支原体DNA序列(1)的特异性及PCR扩增引物，该序列长度为215bp。通过对人类生殖道脲解支原体感染标本的PCR扩增，克隆，获得该序列，测序证明与预计序列一致。再经生物信息学方法分析，基因芯片杂交分析，结果证实了该序列对于脲解支原体的特异性。本发明作为基因芯片诊断的探针及PCR扩增检测序列，用于脲解支原体的诊断。用本发明建立的临床检测技术所使用的方法具有快速、准确、操作简便、成本低等优点。 ...

Contrast design scheme of gene chip for clinical diagnosis

The present invention relates to contrast design scheme of gene chip for clinical diagnosis, and belongs to the field of biomedicine technology. Human beta-actin gene and plant specific DNA segment are used as positive contrast probe in chip detection for testing the operation of gene chip in clinical detection. The present invention can judge the correctness in the operation of chip detection, and is suitable for contrast design of all clinical detection gene chip.

一段脲解支原体DNA序列（4）特异性的确定及其应用

The present invention relates to determination of a section of mycoplasma urealyticum DNA sequence (4) specificity and its application, and belongs to the field of biotechnology. Via search and analysis of gene data base information, one section of mycoplasma urealyticum DNA sequence (4) specificity and PCR amplimer are determined, with the sequence length being 314 bp. The sequence is obtained through the amplification and cloning of human genital tract mycoplasma urealyticum infection specimen, and its specificity to mycoplasma urealyticum is proved through bioinformatic analysis and gene chip hybridizing analysis. The present invention is used as the probe for gene chip diagnosis and PCR amplification detecting sequence in diagnosing mycoplasma urealyticum. The clinical detection technological method has the advantages of being fast, accurate, simple in operation and low in cost.

一段淋球菌DNA序列（2）特异性的确定及其应用

The present invention utilizes the search and analysis of data base to define the specificity of a segmentum of gonococcus DNA sequence (2) and PCR amplification primer, sand sequence length is 204 bp, and said sequence can be obtained by PCR amplification and clone of haman genital tract gonococcus infection specimen. Said invention can be used as probe for making gene chip diagnosis and PCR amplification detection sequence for accurately diagnosing gonococcus infection.

一段脲解支原体DNA序列（2）特异性的确定及其应用

A determination to the specificity of a urea-decomposing mycoplasma DNA sequence (2) segment includes searching and analyzing the gene database to determine the specificity of said sequence segment (288 bp) and the primer of PCR amplification, PCR amplificating and cloning of the human genetic tract's urea-decomposing mycoplasma infectious specimen to obtain the sequence, sequencing it to prove that it is constent with the predicted sequence, biological information analysis, and gene chip cross analyzing to prove its specifcity to urea-decomposing mycoplasma. It can be used as the probe of gene chip diagnosis and the test sequence of PCR amplification to diagnose urea-decomposing mycoplasma.