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    • 4. 发明公开
    • 병원성 바이러스 검출 방법
    • 检测病原性病毒的方法
    • KR1020130138372A
    • 2013-12-19
    • KR1020120061874
    • 2012-06-11
    • 충북보건과학대학교 산학협력단주식회사 에스씨티
    • 박기랑조영화최영국
    • C12Q1/68C12N15/11C12Q1/04
    • C12Q1/04C12Q1/686G01N33/56983
    • The present invention relates to a method for detecting a pathogenic virus comprising: (a) a step for extracting a specific gene specifying the virus from virus genome; (a-1) a step for designing primers based on the detectable specific region of the extracted specific gene; (a-2) a step for cloning by inserting the extracted specific gene into a transferring vector; (b) a step for performing nucleic acid amplification using the vector, wherein the specific gene is inserted, and a set of primers; and (c) a step for detecting by electrophoresis of the amplified nucleic acid product. The set of primers can be prepared as: i) a pair of primers comprising a forward primer having a first sequence of sequence listing and a reverse primer having a second sequence of the sequence listing; or ii) a pair of primers comprising a forward primer having a third sequence of sequence listing and a reverse primer having a fourth sequence of the sequence listing. As is mentioned above, by the present invention, an infenitesimal contamination in biological products can be detected using Polymerase chain reaction (PCR) which is a detecting technique by amplifying small amount of DNA.
    • 本发明涉及一种用于检测病原体病毒的方法,包括:(a)从病毒基因组提取特定病毒的特定基因的步骤; (a-1)基于提取的特异性基因的可检测特异性区域设计引物的步骤; (a-2)通过将提取的特异性基因插入转移载体来进行克隆的步骤; (b)使用载体进行核酸扩增的步骤,其中插入特异性基因和一组引物; 和(c)通过电泳检测扩增的核酸产物的步骤。 该组引物可以如下制备:i)一对引物,其包含具有第一序列表序列的正向引物和具有序列表第二序列的反向引物; 或ii)一对引物,其包含具有第三序列表序列的正向引物和具有序列表第四序列的反向引物。 如上所述,通过本发明,可以使用作为通过扩增少量DNA的检测技术的聚合酶链反应(PCR)来检测生物制品中的微小污染物。