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公开(公告)号：US20210214780A1
公开(公告)日：2021-07-15
申请号：US17134502
申请日：2020-12-28
Applicant: Industrial Technology Research Institute
Inventor： Pei-Shin Jiang , Jenn-Yeh Fann , Hung-Chi Chien , Yu-Yu Lin , Chih-Lung Lin
IPC: C12Q1/6855 , C12Q1/6869
Abstract: Methods of amplifying and determining a target nucleotide sequence are provided. The method of amplifying the target nucleotide sequence includes the following steps. A first adaptor and a second adaptor are linked to two ends of a double-stranded nucleic acid molecule with a target nucleotide sequence respectively to form a nucleic acid template, in which the first adaptor includes a Y-form adaptor or a hairpin adaptor and the second adaptor is a hairpin adaptor. Then, a PCR amplification cycle is performed on the nucleic acid template to obtain a PCR amplicon of the target nucleotide sequence.
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公开(公告)号：US10533160B2
公开(公告)日：2020-01-14
申请号：US15838361
申请日：2017-12-12
Applicant: Industrial Technology Research Institute
Inventor： Yi-Chau Huang , Huai-Lo Lee , Yu-Yin Tsai , Chih-Lung Lin
Abstract: A recombinant protein and a preparation method and application thereof are provided. The recombinant protein includes a peptide, and the peptide includes an amino acid sequence after substitution of the sequence of SEQ ID NO: 1. The substitution includes at least one selected from the group consisting of the following substitutions: the amino acid at position 182 of SEQ ID NO: 1 is substituted with aspartic acid (Asp); the amino acid at position 268 of SEQ ID NO: 1 is substituted with aspartic acid (Asp); and the amino acid at position 384 of SEQ ID NO: 1 is substituted with tyrosine (Tyr). The recombinant protein is suitable for detecting glycated hemoglobin.
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公开(公告)号：US11920190B2
公开(公告)日：2024-03-05
申请号：US17134502
申请日：2020-12-28
Applicant: Industrial Technology Research Institute
Inventor： Pei-Shin Jiang , Jenn-Yeh Fann , Hung-Chi Chien , Yu-Yu Lin , Chih-Lung Lin
IPC: C12Q1/6855 , C12Q1/6869
CPC classification number: C12Q1/6855 , C12Q1/6869
Abstract: Methods of amplifying and determining a target nucleotide sequence are provided. The method of amplifying the target nucleotide sequence includes the following steps. A first adaptor and a second adaptor are linked to two ends of a double-stranded nucleic acid molecule with a target nucleotide sequence respectively to form a nucleic acid template, in which the first adaptor includes a Y-form adaptor or a hairpin adaptor and the second adaptor is a hairpin adaptor. Then, a PCR amplification cycle is performed on the nucleic acid template to obtain a PCR amplicon of the target nucleotide sequence.
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公开(公告)号：US20180164196A1
公开(公告)日：2018-06-14
申请号：US15381116
申请日：2016-12-16
Applicant: Industrial Technology Research Institute
Inventor： Chien-An Chen , Wen-Ching Lee , Tzu-Hui Wu , Pei-Shin Jiang , Ping-Jung Wu , Ruey-Shyan Hong , Hsiao-Jou Chang , Chun-Chieh Huang , Ting-Hsuan Chen , Chih-Lung Lin
CPC classification number: G01N1/36 , B01L3/508 , B01L7/52 , B01L2200/025 , B01L2200/0605 , B01L2200/0621 , B01L2200/0631 , B01L2300/0681 , B01L2300/0832 , B01L2300/0867 , B01L2400/0478 , B01L2400/0622 , B01L2400/0644 , C12M1/42 , C12N15/10 , G01N33/48
Abstract: A biological sample processing device includes a base, a purification unit, a metering unit and a first tube. The purification unit is disposed on the base and is configured to purify a sample. The metering unit is disposed on the base and has an inlet, at least one metering trough and an overflow trough. The inlet is connected to the purification unit via the first tube, and the metering trough is connected between the inlet and the overflow trough. The sample from the purification unit is configured to enter the metering unit through the inlet to be moved toward the metering trough, and to be moved toward the overflow trough after the metering trough is filled with the sample.
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公开(公告)号：US09309501B2
公开(公告)日：2016-04-12
申请号：US14138155
申请日：2013-12-23
Applicant: Industrial Technology Research Institute
Inventor： Tseng-Huang Liu , Pei-Shin Jiang , Chih-Lung Lin , Su-Jan Lee , Chao-Hung Kao
IPC: C12N9/12
CPC classification number: C12N9/1252
Abstract: Isolated DNA polymerase and the mutant DNA polymerases thereof are provided. The DNA polymerases have good thermostability.
Abstract translation: 提供了分离的DNA聚合酶及其突变型DNA聚合酶。 DNA聚合酶具有良好的热稳定性。
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Patent Agency Ranking
公开(公告)号：US20250081632A1
公开(公告)日：2025-03-06
申请号：US18818614
申请日：2024-08-29
Applicant: Industrial Technology Research Institute
Inventor： Hsin-Chung Wu , Chun-Wei Su , Tzu-Ting Lin , En-Yu Pan , Yu-Tsung Chiu , Chih-Lung Lin , Teng-Yu Wang , Chiou-Chu Lai , Ying-Jung Chiang
IPC: H01L31/048 , H01L31/024
Abstract: A solar cell module includes a first substrate, a second substrate, at least one cell unit, a first packaging film, a second packaging film, a first protective layer, a second protective layer, and a plurality of support members. The first substrate and the second substrate are disposed opposite to each other. The cell unit is disposed between the first substrate and the second substrate. The first packaging film is disposed between the cell unit and the first substrate. The second packaging film is disposed between the cell unit and the second substrate. The first protective layer is disposed between the cell unit and the first packaging film. The second protective layer is disposed between the cell unit and the second packaging film. The support members are respectively disposed between the first packaging film and the second packaging film and surround at least two opposite sides of the cell unit.
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公开(公告)号：US11931783B2
公开(公告)日：2024-03-19
申请号：US17072349
申请日：2020-10-16
Applicant: INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE
Inventor： Teng-Yu Wang , Chih-Lung Lin , Cheng Chuan Wang
Abstract: A recycle apparatus includes a conveyor, a flattening device, and a cutting tool. The conveyor includes a first roller and a second roller opposite to each other. The flattening device is located aside the first roller and the second roller. The cutting tool is located aside the flattening device. The flattening device is located between the first roller and the second roller of the conveyor and the cutting tool. The first roller and the second roller is configured to press and feed the photovoltaic module to the flattening device for allowing the photovoltaic module to be flattened by the flattening device, and then the flattened photovoltaic module is fed to the cutting tool by the first roller and the second roller for allowing the back sheet to be separated from the glass sheet assembly by the cutting tool.
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公开(公告)号：US20180163184A1
公开(公告)日：2018-06-14
申请号：US15838361
申请日：2017-12-12
Applicant: Industrial Technology Research Institute
Inventor： Yi-Chau Huang , Huai-Lo Lee , Yu-Yin Tsai , Chih-Lung Lin
Abstract: The fructosyl amino acid oxidase (FPOX-CE) of other species, wild-type fructosyl amino acid oxidase (PnFPOX), and the recombinant proteins (PnFPOX-SS, PnFPOX-DS, and PnFPOX-TS) were respectively dissolved in a 100 mM potassium phosphate buffer (pH value of 8.0) to achieve a concentration of 0.05 mg/ml, and after a heat treatment at 25° C. to 60° C. for 10 minutes, the oxidase activities of the above-mentioned fructosyl amino acid oxidases and recombinant proteins were measured. At the same time, thermal stability (%) was calculated based on the following formula: thermal stability=(value of oxidase activity after heat treatment)/(value of oxidase activity without heat treatment)×100%.
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公开(公告)号：US20140186894A1
公开(公告)日：2014-07-03
申请号：US14138155
申请日：2013-12-23
Applicant: Industrial Technology Research Institute
Inventor： Tseng-Huang Liu , Pei-Shin Jiang , Chih-Lung Lin , Su-Jan Lee , Chao-Hung Kao
CPC classification number: C12N9/1252
Abstract: Isolated DNA polymerase and the mutant DNA polymerases thereof are provided. The DNA polymerases have good thermostability.
Abstract translation: 提供了分离的DNA聚合酶及其突变型DNA聚合酶。 DNA聚合酶具有良好的热稳定性。
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公开(公告)号：US11811357B2
公开(公告)日：2023-11-07
申请号：US17134807
申请日：2020-12-28
Applicant: INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE
Inventor： Teng-Yu Wang , Chih-Lung Lin , Mu-Hsi Sung , Neng-Wen Hsieh , Chin-Yueh Li
Abstract: The disclosed embodiments relate to a dismantling device configured for a frame of a PV module. The dismantling device includes a connection portion, a first holding portion, and a second holding portion. The first holding portion is connected to the connection portion and configured to press against one of an inner wall and outer wall of the frame. The second holding portion is slidably disposed on the connection portion and movably closer to or away from the first holding portion along a sliding direction. The second holding portion is configured to press against the other one of the inner wall and the outer wall so as to clamp the frame with the first holding portion and to distort the frame.
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