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一种用于枇杷控梢促花的制剂

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摘要

本发明公开了一种用于枇杷控梢促花的制剂，按重量份数计，包括：纤维素降解酶50～80份，15％粉锈宁0.1～0.5份；还公开了其相应的可使用的辅基和优选的使用方法。其通过促进枇杷内吸收循环和模拟枝干衰亡的综合作用模式，改变了现有技术中控梢促花的基本原理，调动枇杷本体的生长调节功能，达到控梢促花的目的；其各组分及其代谢产物均在枇杷体内均无残留，所以各组分所组合而成的酶制剂具备无残留的特性，加之所使用辅基同样无毒无害，故能够有效地保障了枇杷优异的食、药用价值；且具备制剂制备和使用简单，效果显著的特点；因此，具备优异的推广价值。

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公开/公告号CN108669089B

专利类型发明专利
公开/公告日2021-02-09

原文格式PDF
申请/专利权人会东县隆峰农业农机服务有限公司;
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申请/专利号CN201810425953.0
发明设计人杨世春;晏琳;张华;张才彬;王彩;张国薇;王浩;王燕;
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申请日2018-05-04
分类号A01N63/50(20200101);A01N43/653(20060101);A01P21/00(20060101);
代理机构51230 成都弘毅天承知识产权代理有限公司;
代理人白小明
地址 615000 四川省凉山彝族自治州会东县鲹鱼河镇光明街261号
入库时间 2022-08-23 11:31:38

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1. 一种用于枇杷控梢促花的制剂 [P] . 中国专利： CN108669089B . 2021.02.09
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3. Polinucleotu00eddeo insulated tape of expression, host cell, isolated transgenic non-human animal polypeptide, which has been modified to express a polypeptide mutant with resistance to ALK, antibody that binds specifically to a polypeptide mutant with resistance to ALK, kit p For detection of a mutation with resistance to ALK inhibitor in a biological sample, and,Methods for evaluating a biological sample as a mutation with resistance to ALK inhibitor, for diagnosing a cancer that is resistant to or is likely to develop resistance to at least one inhibitor of kinase small molecule ALK, to evaluate a biological sample that Anto a mutation with resistance to ALK inhibitor.For diagnosing a cancer that is resistant to or is likely to develop resistance to at least one inhibitor of kinase small molecule ALK, to assess the biological sample as a mutation with resistance to ALK inhibitor, a cancer that is resistant to dianosticar Or is likely to develop resistance to PF - 02341066 in a pati [P] . BR112012026239A2 . 2016-11-29

机译：修饰的多聚核苷酸绝缘带，宿主细胞，分离的转基因非人类动物多肽，经过修饰以表达对ALK具有抗性的多肽突变体，与对ALK具有抗性的多肽突变体特异性结合的抗体，试剂盒p用于检测生物样品中对ALK抑制剂具有抗性的突变，以及用于评估生物样品为对ALK抑制剂具有抗性的突变的方法，用于诊断对至少一种对ALK抑制剂具有抗性或可能发展出抗性的癌症激酶小分子ALK，以评估Anto对ALK抑制剂具有抗性的突变的生物样品。用于诊断对至少一种激酶小分子ALK抑制剂具有抗药性或可能产生抗性的癌症，以评估该生物样品作为对ALK抑制剂有抗性的突变，即对狄诺司他抗性或可能对PF产生抗药性的癌症-02341066
4. use of a compound selected from the group consisting of a proteasome inhibitor, an autophagy inhibitor, a lysosomal inhibitor, an golgi er protein transport inhibitor, an hsp90 chaperonin inhibitor, a heat shock response activator, a and a histone deacetylase inhibitor, use of 11-cis-retinal or 9-cis-retinal and a compound selected from the group consisting of a proteasome inhibitor, an autophagy inhibitor, a lissosomal inhibitor, a er to golgi protein, a hsp90 chaperonin inhibitor, a heat shock response activator, a glycosidase inhibitor, and a histone deacetylase inhibitor, a method for increasing the amount of a biochemically functional conformation of a protein in a cell, composition pharmaceutical for the treatment of an ocular pcd, pharmaceutical composition for the treatment of retinitis pigmentosa, kit for the treatment of an ocular pcd, kit for the treatment retinitis pigmentosa, method for identifying a compound useful for the treatment of an individual having an ocular pcd, [P] . BRPI0615962A2 . 2011-05-31

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