Polypeptide
老挝专利「Polypeptide」是 DIP 公开可查的知识产权档案，由 Helsingin Yliopisto 于 2012-11-29 提交申请，当前状态为等待形式审查。公开档案中可核验：申请号 P/313，DIP 编号 LAP313，主管局代码 LA，保护类型 Patent - PCT National Phase。时间线要点：公开/公告日 2026-01-09。技术或外观分类记载为 A01H 5/00、C12N 15/82、C12N 9/10。发明人 / 设计人包括 Ana Campilho、Anne VATEN、Annelie Carlsbecker、Ari Pekka Mahonen、Jan Dettmer 等。代理机构 / 代理人记载为 Tilleke & Gibbins Lao Co., Ltd.。公开摘要提示：The present invention relates to polypeptide, or a fragment thereof, capable of enhancing callose biosynthesis and/or accumulation, wherein…。
P/313
图样
基础信息
- 类型
- 专利
- 申请号
P/313- 状态
- 等待形式审查
- 申请人
- Helsingin Yliopisto
- 代理机构
- Tilleke & Gibbins Lao Co., Ltd.
- 申请日期
- 2012-11-29
- 公开 / 公告日
- 2026-01-09
- 保护类型
- Patent - PCT National Phase
- 优先权
- FI · 20116212 · 2011-12-01
- 申请人地址
- Helsingin Yliopisto · YliopisTonkatu 4, 00014 Helsingin Yliopisto · FI
- 代理地址
- Tilleke & Gibbins Lao Co., Ltd. · No. 302/1B, 3rd Floor, Vieng Vang Tower, Unit 15 Boulichan Road, Dongpalan Thong Village, Sisattanak District, Vientiane · LA
- 国际分类
- A01H 5/00 · C12N 15/82 · C12N 9/10
- 商品 / 服务
- —
办理流程
根据当前状态动态标注-
提交申请
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形式审查 进行中
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实质审查
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公开
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授权
关联分析
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摘要
The present invention relates to polypeptide, or a fragment thereof, capable of enhancing callose biosynthesis and/or accumulation, wherein at least one of the conserved amino acid residues selected from the group consisting of residue corresponding to R84 of SEQ ID NO: 1, residue corresponding to R1926 or SEQ ID NO: 1 and residue corresponding to P189 of SEQ ID NO: 1, of the polypeptide or a fragment thereof, is modified by a mutation selected from the group consisting of substitution and deletion.
The present invention relates to polypeptide, or a fragment thereof, capable of enhancing callose biosynthesis and/or accumulation, wherein at least one of the conserved amino acid residues selected from the group consisting of residue corresponding to R84 of SEQ ID NO: 1, residue corresponding to R1926 or SEQ ID NO: 1 and residue corresponding to P189 of SEQ ID NO: 1, of the polypeptide or a fragment thereof, is modified by a mutation selected from the group consisting of substitution and deletion.
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