VECTOR AND METHOD FOR SCREENING FUNCTIONAL ANTIGEN-BINDING PROTEIN

    公开(公告)号:EP4317549A1

    公开(公告)日:2024-02-07

    申请号:EP22779050.8

    申请日:2022-03-30

    发明人: ZHOU, Chen

    IPC分类号: C40B50/06 C40B40/02

    摘要: A method for selecting a functional antigen-binding protein. The method comprises the step of constructing an expression vector, by means of a phage display technique and/or a cell display technique, using a light chain or a fragment thereof of a reference antigen-binding protein with a known sequence and function, or a heavy chain or a fragment thereof of the reference antigen-binding protein, thereby selecting a functional antigen-binding protein that binds to the same epitope as the reference antigen-binding protein. Further provided is a functional antigen-binding protein obtained by means of the method.

    METHOD FOR RAPIDLY CONSTRUCTING CYCLIZED LIBRARY AND RING-FORMING LINKER

    公开(公告)号:EP4273307A1

    公开(公告)日:2023-11-08

    申请号:EP20967409.2

    申请日:2020-12-29

    IPC分类号: C40B40/06 C40B50/06 C40B80/00

    摘要: The present invention falls within the field of biotechnology, and specifically discloses a method for constructing a cyclized library and a ring-forming linker. The method comprises: 1) breaking a DNA sequence into fragments; 2) enabling two ends of the broken fragment to form 3' end protrusions; and 3) cyclizing the fragment with 3' end protrusions to form a ring-shaped library by means of a ring-forming linker, wherein the ring-forming linker is a double chain which is not completely paired and has 3' end protrusion at both ends, and the 3' end protrusion of the ring-forming linker is complementary to the 3' end protrusion of the broken fragment. According to the present invention, an A-sticky end of the end is formed by means of repairing the end of and the adding A to the broken DNA fragment, and same is then complementary to the specifically designed linker T sticky end to form a cyclized structure, and the connection at the gap is completed under the action of a ligase.

    IN-VITRO CULTURE, INDUCTION, ACTIVATION AND CRYOPRESERVATION METHOD AND CELL BANK ESTABLISHMENT FOR IMMUNE CELLS

    公开(公告)号:EP4148123A1

    公开(公告)日:2023-03-15

    申请号:EP20934683.2

    申请日:2020-05-26

    IPC分类号: C12N5/0783 C40B50/06 A01N1/02

    摘要: The present invention discloses an in-vitro culture, induction, activation and cryopreservation method and cell bank establishment for immune cells. The method includes the follows: using a dedicated amplification medium of immune cells to perform first-stage amplification culture on mononuclear cells to obtain preliminarily amplified immune cells; using a dedicated induction medium of immune cells to perform second-stage induction and amplification culture on the preliminarily amplified immune cells to obtain induced immune cells; using a dedicated activation medium of immune cells to perform third-stage activation and amplification culture on the induced immune cells to obtain a large number of immune cells with activation functions; using a dedicated cryopreserving fluid of immune cells to cryopreserve the immune cells to obtain cryopreserved immune cells; and performing preservation according to ABO/RH typing and HLA typing; and establishing an information file of immune cells for retrieval to construct an immune cell bank.

    METHOD FOR BUILDING RNA LIBRARY AND KIT
    9.
    发明公开

    公开(公告)号:EP3848473A1

    公开(公告)日:2021-07-14

    申请号:EP18932607.7

    申请日:2018-09-05

    申请人: BGI Shenzhen

    IPC分类号: C12Q1/68 C40B50/06

    摘要: Provided are an RNA library construction method and a specialized kit thereof. The method for preparing an RNA library includes the following steps: extracting RNA and performing fragmentation; adding a tail to 3' end; ligating an adaptor to 5' end and hybridizing with a DNA probe mixture; the DNA probe mixture is composed of several DNA probes that are reverse complementary to an RNA that is expected to be removed; removing RNA from the hybrid and removing DNA; performing reverse transcription and PCR amplification to obtain a library solution. The present invention combines poly A tailing and 5'end ligation. The RNA content in the system can be quickly increased by polyA tailing, thereby avoiding subsequent purification losses.