Gene therapy DNA vectors based on VTVAF17

    公开(公告)号:US12128112B2

    公开(公告)日:2024-10-29

    申请号:US17272587

    申请日:2019-08-14

    Abstract: Produced the gene therapy DNA vectors based on the gene therapy DNA vector VTvaf17 for the treatment of diseases featuring disruption of mucociliary transport, mucolytic function and development of mucostasis. The gene therapy DNA vector contains the coding region of the SKI, TGFB3, TIMP2 or FMOD therapeutic genes. Methods of producing or use a gene therapy DNA vector based on gene therapy DNA vector VTvaf17 carrying SKI, TGFB3, TIMP2 or FMOD therapeutic genes. The methods of producing strain for production of gene therapy DNA vector for treatment of diseases featuring disruption of mucociliary transport and development of mucostasis. Escherichia coli strain SCS 110-AF/VTvaf17-SKI, SCS 110-AF/VTvaf17-TGFB3, SCS110-AF/VTvaf17-TIMP2 or SCSI 10-AF/VTvaf17-FMOD obtains by the method described above carrying gene therapy DNA vector VTvaf17-SKI, VTvaf17-TGFB3, VTvaf17-TIMP2 or VTvaf17-FMOD. The method of producing a gene therapy DNA vector carrying SKI, TGFB3, TIMP2 or FMOD therapeutic gene uses on an industrial scale.

    HOMOGENEOUS METHOD TO PREPARE SPERM DNA FROM SEXUAL ASSAULT CASES

    公开(公告)号:US20240301392A1

    公开(公告)日:2024-09-12

    申请号:US18655262

    申请日:2024-05-05

    Applicant: Alex Garvin

    Inventor: Alex Garvin

    CPC classification number: C12N15/1003

    Abstract: The present invention provides a method for the isolation of sperm DNA from swabs taken from rape victims without having to perform a change in buffers. Non-sperm cells from the victim are digested with an enzyme and solubilized, and then in the same buffer an enzyme capable of digesting soluble DNA is added and the victim's DNA is degraded, leaving only the rapist's DNA intact. Since no change of buffer is needed, no centrifugation or filtration steps are needed. The inventive method has utility particularly in the forensic science field.

    METHOD FOR ISOLATING AND PURIFYING NUCLEIC ACID SOLID FROM BIOLOGICAL MATERIAL

    公开(公告)号:US20240218350A1

    公开(公告)日:2024-07-04

    申请号:US18028746

    申请日:2021-09-28

    Inventor: Xianglong YANG

    CPC classification number: C12N15/1003

    Abstract: The present invention discloses a method for isolating and purifying solid nucleic acids from biomaterials comprising the steps of (1) mixing the liquid containing naked nucleic acids with a precipitant; centrifuging at room temperature, pouring the supernatant into a new centrifuge tube; (2) adding isopropanol to the new centrifuge tube, mixing well, standing at room temperature, centrifuging, producing a solid, discarding other than the solid; washing, obtaining solid RNAs or solid mixtures of RNAs and DNAs and storing. The invention uses a homogenization-dissociation reagent to homogenize biomaterials, and a liquid containing naked nucleic acids can be easily obtained without heating, which can be used to extract solid RNAs and solid DNAs. By adding a compound that removes secondary metabolites of cells to the homogenization-dissociation reagent, vascular plant RNA, woody plant RNA, and both solid RNAs and solid DNA can be extracted from human blood. The solid RNAs and solid DNAs obtained by the present invention can be stored at room temperature for one month or below −20° C. for one year.

    COMPOSITION AND THE USE OF CELL LYSIS REAGENTS

    公开(公告)号:US20240026339A1

    公开(公告)日:2024-01-25

    申请号:US18349394

    申请日:2023-07-10

    CPC classification number: C12N15/1003

    Abstract: The present invention relates to amphiphiles and specifically the amphiphiles that can be used as cell lysis reagents. The invention reveals the amphiphiles as well as their combinations for efficiently lysing the mammalian cells under relatively mild conditions that are compatible with a reverse transcription and polymerase chain reaction. The invention reveals the use of mixture of amphiphiles to improve the cell lysis and obtain increased yields of copy DNA during the reverse transcription reaction. The invention also provides a method for increasing the diversity of gene and transcript capture during single-cell RNA-sequencing using droplet microfluidics.

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