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公开(公告)号:US20230295696A1
公开(公告)日:2023-09-21
申请号:US18006375
申请日:2020-07-29
申请人: MGI Tech Co., Ltd.
发明人: Jay Shafto , Radoje Drmanac , Snezana Drmanac , Chongjun Xu , Meihua Gong , Ping Wang , Xiaojuan Long , Wei Zhao , Huan Luo , Hui Jiang , Jian Liu
IPC分类号: C12Q1/6834 , C12Q1/686 , C40B50/18
CPC分类号: C12Q1/6834 , C12Q1/686 , C40B50/18 , C12Q2600/16
摘要: Provided are a method for loading a nucleic acid molecule, for example nucleic acid nanoball (e.g., DNA nanoball (DNB)), on a solid support, and a kit for the method.
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公开(公告)号:US20190330602A1
公开(公告)日:2019-10-31
申请号:US16505121
申请日:2019-07-08
申请人: MGI TECH CO., LTD.
发明人: Lin Wang , Fen Liu , Yuliang Dong , Wenwei Zhang , Chongjun Xu , Drmanac Snezana
IPC分类号: C12N9/12 , C12Q1/6869
摘要: Disclosed in the present disclosure is a recombinant DNA polymerase. The recombinant DNA polymerase is any one selected from: A) a protein, having amino acid modifications at positions 408, 409 and 485, and at least one of amino acid modification(s) at positions 53, 59, 199, 243, 526, 558, 613, 641, 671, 673, 674, 692 and 709 compared to the amino acid sequence of a wild-type KOD DNA polymerase; B) a protein derived from the protein in A), formed by deleting amino acids 1 to 29 from a C-terminus of the protein in A) and keeping the remaining amino acids unchanged; and C) a protein derived from the protein in A) or B), formed by connecting a tag to the N-terminus or C-terminus of the amino acid sequence of the protein in A) or B), wherein the protein in A), B) and C) has DNA polymerase activity.
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公开(公告)号:US11993813B2
公开(公告)日:2024-05-28
申请号:US16643161
申请日:2018-07-06
申请人: MGI TECH CO., LTD.
发明人: Erkai Liu , Wenwei Zhang , Ao Chen , Chongjun Xu
IPC分类号: C12Q1/68 , C07H21/00 , C12Q1/6811 , C12Q1/6853 , C12Q1/6874 , C12Q1/6855
CPC分类号: C12Q1/6874 , C07H21/00 , C12Q1/68 , C12Q1/6811 , C12Q1/6853 , C12Q1/6855 , C12Q1/6874 , C12Q2521/307 , C12Q2525/197 , C12Q2531/137 , C12Q2537/157 , C12Q1/6874 , C12Q2523/107 , C12Q2525/197 , C12Q2531/137 , C12Q2537/157
摘要: A nucleic acid probe and a nucleic acid sequencing method for performing sequencing while ligating nucleic acids. The nucleic acid probe is a DNA sequencing probe, comprising a first moiety, a second moiety, a linker, and a detectable label. A base of the first moiety is A, T, U, C, or G, a base of the second moiety is a random base and/or a universal base, and 3 bases or more are present in the second moiety. The first moiety and the second moiety are ligated via the linker, the connection between the first moiety and the ligation can be cleaved, and the detectable label is ligated to the second moiety or the linker. The above probe, a combination formed therewith, or a sequencing method using the same can reduce the number or types of probes in nucleic acid sequencing, thereby reducing cost.
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公开(公告)号:US10961519B2
公开(公告)日:2021-03-30
申请号:US16657713
申请日:2019-10-18
申请人: MGI TECH CO., LTD.
发明人: Huanhuan Liu , Yue Zheng , Yujun Zhou , Xi Zhang , Zhougang Zhang , Yuliang Dong , Wenwei Zhang , Chongjun Xu , Snezana Drmanac
摘要: Provided are a phi29 DNA polymerase mutant with increased thermo stability, a method for preparing the mutant, the use of the mutant, and a method for increasing the stability of the phi29 DNA polymerase.
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公开(公告)号:US10883091B2
公开(公告)日:2021-01-05
申请号:US16505121
申请日:2019-07-08
申请人: MGI TECH CO., LTD.
发明人: Lin Wang , Fen Liu , Yuliang Dong , Wenwei Zhang , Chongjun Xu , Snezana Drmanac
IPC分类号: C12N9/12 , C12Q1/6869
摘要: Disclosed in the present disclosure is a recombinant DNA polymerase. The recombinant DNA polymerase is any one selected from: A) a protein, having amino acid modifications at positions 408, 409 and 485, and at least one of amino acid modification(s) at positions 53, 59, 199, 243, 526, 558, 613, 641, 671, 673, 674, 692 and 709 compared to the amino acid sequence of a wild-type KOD DNA polymerase; B) a protein derived from the protein in A), formed by deleting amino acids 1 to 29 from a C-terminus of the protein in A) and keeping the remaining amino acids unchanged; and C) a protein derived from the protein in A) or B), formed by connecting a tag to the N-terminus or C-terminus of the amino acid sequence of the protein in A) or B), wherein the protein in A), B) and C) has DNA polymerase activity.
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公开(公告)号:US11104889B2
公开(公告)日:2021-08-31
申请号:US16633942
申请日:2017-08-09
申请人: MGI Tech Co., Ltd.
发明人: Zhougang Zhang , Huanhuan Liu , Yue Zheng , Yujun Zhou , Xing Liu , Yuliang Dong , Chongjun Xu , Wenwei Zhang
IPC分类号: C12N9/12
摘要: Provided are a group of phi29 DNA polymerase mutants having increased thermal stability and use thereof. The phi29 DNA polymerase mutants are proteins obtained by performing point mutation A and/or point mutation B and/or point mutation C on phi29 DNA polymerase, the point mutation A meaning that an amino acid residue M at position 97 of the phi29 DNA polymerase is mutated to other amino acid residue, the point mutation B meaning that an amino acid residue L at position 123 of the phi29 DNA polymerase is mutated into other amino acid residue, and the point mutation C meaning that an amino acid residue E at position 515 of the phi29 DNA polymerase is mutated to other amino acid residue. The stability of the phi29 DNA polymerase mutants is higher than that of a wild-type phi29 DNA polymerase.
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公开(公告)号:US11485966B2
公开(公告)日:2022-11-01
申请号:US16754713
申请日:2017-10-11
发明人: Hui Wang , Xun Xu , Jin Yang , Ao Chen , Chongjun Xu , Wenwei Zhang
摘要: The present invention provides a method for improving the loading of nucleic acid on a solid support by contacting the solid support with a poloxamer-containing reagent. The present invention also provides a method for improving the stability of a nucleic acid on a solid support, comprising contacting a nucleic acid molecule with a partially double-strand oligonucleotide before or after loading the nucleic acid molecule on a solid support, so as to cause the nucleic acid molecule to hybridize with the oligonucleotide. The present invention also provides a combined use of the two methods.
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公开(公告)号:US20230272467A1
公开(公告)日:2023-08-31
申请号:US18144121
申请日:2023-05-05
发明人: Jin Yang , Xun Xu , Hui Wang , Bin Xie , Zhuokun Li , Shengming Zhao , Ao Chen , Chongjun Xu , Wenwei Zhang , Ming Ni
IPC分类号: C12Q1/6869 , C12Q1/6876 , G01N21/64
CPC分类号: C12Q1/6869 , C12Q1/6876 , G01N21/6486 , B01L2200/10
摘要: The present invention provides a method for sequencing a nucleic acid using an immersion reaction protocol. The immersion reaction protocol comprises sequentially immersing a solid support having nucleic acid molecules immobilized thereon in different reaction containers to realize nucleic acid sequencing.
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公开(公告)号:US11692221B2
公开(公告)日:2023-07-04
申请号:US16635131
申请日:2017-08-01
发明人: Jin Yang , Xun Xu , Hui Wang , Bin Xie , Zhuokun Li , Shengming Zhao , Ao Chen , Chongjun Xu , Wenwei Zhang , Ming Ni
IPC分类号: C12Q1/6869 , C12Q1/6876 , G01N21/64
CPC分类号: C12Q1/6869 , C12Q1/6876 , G01N21/6486 , B01L2200/10
摘要: The present invention provides a method for sequencing a nucleic acid using an immersion reaction protocol. The immersion reaction protocol comprises sequentially immersing a solid support having nucleic acid molecules immobilized thereon in different reaction containers to realize nucleic acid sequencing.
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公开(公告)号:US10883092B2
公开(公告)日:2021-01-05
申请号:US16606148
申请日:2017-04-18
申请人: MGI TECH CO., LTD.
发明人: Yue Zheng , Zhougang Zhang , Yuliang Dong , Wenwei Zhang , Chongjun Xu , Snezana Drmanac
摘要: Provided are a phi29 DNA polymerase and an encoding gene and an application thereof. The phi29 DNA polymerase is C1) or C2): C1) is a protein with DNA polymerase activity obtained by substituting at least one of the 58th, 61st, 94th, 96th, 119th, and 155th amino acid residues in the amino acid sequence of a wild type phi29 DNA polymerase as shown in SEQ ID NO: 2 in the sequence listing; and C2) is a fusion protein obtained by linking a label to the N-terminus and/or C-terminus of the protein represented by C1). A 3′-5′exonuclease of the phi29 DNA polymerase has activity lower than that of the wild type phi29 DNA polymerase, and can efficiently and continuously synthesize DNA during amplification and sequencing.
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