METHOD OF DETECTING CHARACTER STRING PATTERN AT HIGH SPEED USING LAYERED SHIFT TABLES
    6.
    发明申请
    METHOD OF DETECTING CHARACTER STRING PATTERN AT HIGH SPEED USING LAYERED SHIFT TABLES 有权
    使用层状移位表检测高速字符模式的方法

    公开(公告)号:US20110066631A1

    公开(公告)日:2011-03-17

    申请号:US12443802

    申请日:2008-09-22

    IPC分类号: G06F17/30

    CPC分类号: G06F7/02 G06F2207/025

    摘要: A character string pattern matching method for detecting the presence of at least one of N (N is a natural number equal to or greater than 2) patterns in specific text shifts a detection location across text by a maximum shift length using single-byte character-based layered SHIFT tables, thereby increasing a pattern matching speed as compared with the prior art pattern matching algorithms.

    摘要翻译: 用于检测特定文本中N(N是等于或大于2的自然数)的模式中的至少一个的字符串模式匹配方法使用单字节字符 - 基于分层的SHIFT表,从而与现有技术的模式匹配算法相比增加了模式匹配速度。

    Plasmid having a function of t-vector and expression vector, and expression of the target gene using the same
    7.
    发明申请
    Plasmid having a function of t-vector and expression vector, and expression of the target gene using the same 审中-公开
    具有t载体和表达载体的功能的质粒以及使用其的靶基因的表达

    公开(公告)号:US20060199185A1

    公开(公告)日:2006-09-07

    申请号:US10564880

    申请日:2003-12-31

    CPC分类号: C12N15/64

    摘要: The present invention relates to a plasmid (pHCE-FOREX) functioning as both a T-vector and an expression vector, which is produced by imparting a T-vector function to an HCE promoter derived from a constitutive high-level expression vector and can express a target protein in a simple and rapid manner. Also, the present invention relates to an expression vector having the target gene inserted into the plasmid, and the expression of the target gene using the same. The plasmid of the present invention can be converted into a vector that expresses the target protein by one-step T-vector cloning in a simple and rapid manner. The plasmid converted into the expression vector does not require a re-transformation step and allows the high-level expression of the target protein only by the culturing of transformed E. coli without the addition of an expensive inducer. Thus, according to the present invention, expression plasmids for large amounts of target genes can be produced at the same time, so that the present invention will be very efficient in establishing expression systems for certain genomes and gene groups.

    摘要翻译: 本发明涉及用作T载体和表达载体两者的质粒(pHCE-FOREX),其通过赋予来自组成型高水平表达载体的HCE启动子产生T载体功能而产生,并可表达 目标蛋白以简单快速的方式。 此外,本发明涉及将靶基因插入质粒的表达载体,以及使用该表达载体的靶基因的表达。 本发明的质粒可通过简单快速的一步T载体克隆转化为表达靶蛋白的载体。 转化成表达载体的质粒不需要再转化步骤,并且仅通过培养转化的大肠杆菌而不添加昂贵的诱导物才允许靶蛋白的高水平表达。 因此,根据本发明,可以同时生产大量靶基因的表达质粒,从而本发明在建立某些基因组和基因组的表达系统方面将非常有效。