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公开(公告)号:US20240392266A1
公开(公告)日:2024-11-28
申请号:US18694726
申请日:2022-06-22
Applicant: DAAN GENE CO., LTD.
Inventor: Xiwen JIANG , Aishan LIU , Wei ZHANG , Xiaocheng XIE , Xuelan LU
Abstract: Provided are a Taq polymerase mutant, a preparation method therefor and the use thereof. The Taq polymerase mutant includes an amino acid sequence having at least 70% identity to the amino acid sequence shown in SEQ ID NO:2, wherein the amino acid sequence has mutations occurring at one or more positions selected from the group consisting of: P40, L125, G200, D335, G499, E634, F769 or a combination thereof. The provided Taq polymerase mutant has high amplification activity, can obtain more amplification products compared with wild-type Taq polymerase under the same number of PCR cycles, and moreover, is resistant to whole blood and high salt and has low 5′-3′ exonuclease activity.
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公开(公告)号:US20250002986A1
公开(公告)日:2025-01-02
申请号:US18713019
申请日:2022-07-04
Applicant: DAAN GENE CO., LTD.
Inventor: Xiwen JIANG , Xianlan LIAN , Xiaocheng XIE , Xuelan LU , Haojian XU
IPC: C12Q1/6851
Abstract: Provided in the present invention is a method for preparing a constant-temperature amplification mixed enzyme system. Specifically, disclosed in the present invention is a method comprising: removing the vast majority of glycerol from a prepared glycerol-containing RPA enzyme system by means of dialysis, and then concentrating the enzyme system containing trace glycerol by using an ultrafiltration method. Experiments show that the amplification performance of an RPA mixed enzyme system prepared by means of such method is significantly improved.
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公开(公告)号:US20240254460A1
公开(公告)日:2024-08-01
申请号:US17254376
申请日:2020-11-13
Applicant: Daan Gene Co., Ltd.
Inventor: Xiwen JIANG , Aishan LIU , Zhouquan WANG , Sangsang ZHENG , Jiguang ZHAO , Xianlan LIAN , Xiaocheng XIE , Xuelan LU , Wei ZHANG , Haojian XU , Zhikeng FANG , Zhijian WU
CPC classification number: C12N9/1276 , C12N15/1096 , C12Y207/07049
Abstract: The present invention provides a high temperature resistant reverse transcriptase mutant and its use. In particular, the present invention constructs a reverse transcriptase (M-MLV) mutant library, and the mutants with improved thermostability and higher amplification efficiency are finally screened out by stepwise screening. Under high temperature conditions, the reverse transcription efficiency of the reverse transcriptase mutant of the present invention is greatly improved compared to the wild type.
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