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公开(公告)号:US20220334106A1
公开(公告)日:2022-10-20
申请号:US17721558
申请日:2022-04-15
Applicant: DENSO CORPORATION
Inventor: Akira NUKAZUKA , Mana ASANO , Kei HAYAKAWA , Yuuya YOSHIMITSU , Kazuhiko KANO , Kazuhisa NAKAGAWA , Mai NIIMOTO
IPC: G01N33/53
Abstract: A conjugate includes a binding substance having an activity to bind to a target substance and a label causing a detectable phenomenon. A molecular weight of the binding substance is less than a molecular weight of an immunoglobulin.
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公开(公告)号:US20240353407A1
公开(公告)日:2024-10-24
申请号:US18677132
申请日:2024-05-29
Applicant: DENSO CORPORATION
Inventor: Kei HAYAKAWA , Mana ASANO , Akira NUKAZUKA , Kazuhisa NAKAGAWA , Mai NIIMOTO , Kazuhiko KANO
IPC: G01N33/569 , G01N33/53 , G01N33/543
CPC classification number: G01N33/56983 , G01N33/5308 , G01N33/54386 , G01N2333/165 , G01N2469/10
Abstract: An analysis method for a target substance includes: mixing a conjugate and a sample including the target substance to produce a mixture, the conjugate including a labeled substance and a first binding substance having activity to bind to the target substance; bringing the mixture into contact with a second binding substance fixed to a base; and detecting a phenomenon caused by the labeled substance bound to the target substance that is bound to the second binding substance. The first binding substance is a substance including a nucleic acid, or a substance including an amino acid. The base is provided in each of regions. The target substance to which the second binding substance binds is different among the regions.
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公开(公告)号:US20240309439A1
公开(公告)日:2024-09-19
申请号:US18677551
申请日:2024-05-29
Applicant: Denso Corporation
Inventor: Mai NIIMOTO , Akira Nukazuka , Mana Asano , Kazuhisa Nakagawa , Kei Hayakawa
IPC: C12Q1/6851 , C12Q1/6806 , C12Q1/6876
CPC classification number: C12Q1/6851 , C12Q1/6876 , C12Q1/6806
Abstract: An analysis method detects a target substance using a binding substance. The binding substance includes: a single-stranded nucleic acid preparation having activity to bind to the target substance; and a complementary nucleic acid that forms a base pair with a 3′ terminal region of the single-stranded nucleic acid preparation when the single-stranded nucleic acid preparation is not bound to the target substance, and that dissociates from the 3′ terminal region when the single-stranded nucleic acid preparation is bound to the target substance.
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公开(公告)号:US20220334107A1
公开(公告)日:2022-10-20
申请号:US17721686
申请日:2022-04-15
Applicant: DENSO CORPORATION
Inventor: Akira NUKAZUKA , Mana ASANO , Kei HAYAKAWA , Kazuhiko KANO , Kazuhisa NAKAGAWA , Mai NIIMOTO
IPC: G01N33/53 , G01N33/543
Abstract: A method for detecting a plurality of target substances using a plurality of conjugates each including a binding substance and a label is provided. The binding substance has an activity to bind to one of the target substances and the label causes a detectable phenomenon. The method includes binding at least some of the plurality of conjugates with the plurality of target substances, removing a remainder of the plurality of conjugates that is not bound to the plurality of target substances, and detecting the label. A molecular weight of the binding substance is less than a molecular weight of an immunoglobulin.
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公开(公告)号:US20240301476A1
公开(公告)日:2024-09-12
申请号:US18677250
申请日:2024-05-29
Applicant: DENSO CORPORATION
Inventor: Akira NUKAZUKA , Teppei SAKAI , Mana ASANO , Kei HAYAKAWA , Kazuhisa NAKAGAWA , Mai NIIMOTO
IPC: C12Q1/682 , C12N15/115 , C12Q1/6844 , C12Q1/6876 , G01N33/84
CPC classification number: C12Q1/682 , C12N15/115 , C12Q1/6844 , C12Q1/6876 , G01N33/84 , C12N2310/16
Abstract: An analysis method according to the present disclosure includes: mixing a binding substance and a sample including a target substance. The binding substance includes a nucleic acid region composed of a nucleic acid and having activity to bind to the target substance; removing the binding substance not bound to the target substance; amplifying the nucleic acid region; and detecting a phenomenon caused by the amplification of the nucleic acid region. For example, the analysis method includes: forming a complex of a template nucleic acid including a sequence complementary to a 3′ side sequence of the nucleic acid region; and amplifying the nucleic acid region by an action of a nucleic acid amplifying enzyme using the complex as a starting point.
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