His-MBP tagged DNA endonuclease for facilitated enzyme removal

    公开(公告)号:US11767524B2

    公开(公告)日:2023-09-26

    申请号:US17027747

    申请日:2020-09-22

    Abstract: Disclosed is a product and process, wherein one adds a N-terminal Histamine-Maltose Binding Protein (“MBP”) tag to endonucleases, including restriction endonucleases like Hind III, and binds the tagged fusion protein to a solid support, preferably beads, once the enzyme has digested oligonucleotides in solution, in order to arrest further digestion. Preferred beads for binding the tagged enzyme are magnetic beads, which can easily be removed from solution by binding to a support and then removing it, or can be accumulated by magnetic attraction in a particular region. More preferred are magnetic beads bound to iminodiacetic acid or nitrilotriacetic acid.

    Mutant Taq Polymerase for Increased Salt Concentration or Body Fluids

    公开(公告)号:US20230094503A1

    公开(公告)日:2023-03-30

    申请号:US17487643

    申请日:2021-09-28

    Abstract: The invention includes a mutant Taq polymerase, which can effectively amplify a target sequence under conditions of salt concentration(s) similar to body fluids, including blood, serum or plasma preserved with sodium citrate. The mutant Taq polymerase, or a biologically active fragment thereof, has one or more substitutions differing from the wild type as shown in Table I.

    Taq DNA Polymerase Mutants for Probe qPCR

    公开(公告)号:US20220106576A1

    公开(公告)日:2022-04-07

    申请号:US17470557

    申请日:2021-09-09

    Abstract: Disclosed are Taq DNA polymerase mutants which exhibit enhanced efficiency in qPCR compared to the wild type Taq DNA polymerase. Such mutants include: V62S, V64S, A70F, F73A, A77F, P253G, E255K, D257R, A259F, A271F, L288S, E289K, S357I, L361S, L376S, P382G, T385I, G418P, R419D, E421K, L461S, A472F, E497K, L498S, E524K, D551R, R556D, S679I, L789S, E189K/E507K/E742K (See Sequence Listing Guide for the mutants' amino acid and protein sequences).

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