Kris Zimmerman is an American voice director, casting director, talent coordinator, and voice actor. Zimmerman is most known for directing the English ...
Lance P. Encell - Fitchburg WI, US Keith V. Wood - Mt. Horeb WI, US Monika G. Wood - Mt. Horeb WI, US Mary Hall - Waunakee WI, US Paul Otto - Madison WI, US Gediminas Vidugiris - Fitchburg WI, US Kristopher Zimmerman - Madison WI, US
A polynucleotide encoding a modified luciferase polypeptide. The modified luciferase polypeptide has at least 60% amino acid sequence identity to a wild-type luciferase and includes at least one amino acid substitution at a position corresponding to an amino acid in a wild-type luciferase of SEQ ID NO:1. The modified luciferase polypeptide has at least one of enhanced luminescence, enhanced signal stability, and enhanced protein stability relative to the wild-type luciferase.
Cell Lysis Composition, Methods Of Use, Apparatus And Kit
Laurie Engel - DeForest WI, US John Shultz - Verona WI, US Tonny Johnson - Madison WI, US Kristopher Zimmerman - Madison WI, US Laura Bozek - Madison WI, US Judith Stevens - Oregon WI, US
Assignee:
Promega Corporation
International Classification:
C12N001/08
US Classification:
435/270000
Abstract:
Cell lysis compositions, methods for extracting and isolating proteins and peptides from a host cells using the compositions, kits and apparatus for extracting and isolating protein and peptide molecules from host cells and for detecting for the presence of a protein or peptide. The composition allows for the extraction and isolation of proteins and peptides from host cells without the need for mechanical disruption and with or without isolation of the cells from cell medium. The composition includes at least one surfactant having a hydrophobic-lipophilic balance value in the range from about 11 to about 16; and at least one cell membrane altering compound.
Cell Lysis Composition, Methods Of Use, Apparatus, And Kit
Laurie Engel - DeForest WI, US John Shultz - Verona WI, US Tonny Johnson - Madison WI, US Kristopher Zimmerman - Madison WI, US Laura Bozek - Madison WI, US Judith Stevens - Oregon WI, US
Cell lysis compositions, methods for extracting and isolating proteins and peptides from a host cells using the compositions, kits and apparatus for extracting and isolating protein and peptide molecules from host cells and for detecting for the presence of a protein or peptide. The composition allows for the extraction and isolation of proteins and peptides from host cells without the need for mechanical disruption and with or without isolation of the cells from cell medium. The composition includes at least one surfactant having a hydrophobic-lipophilic balance value in the range from about 11 to about 16; and at least one cell membrane altering compound.
Mutant Protease Biosensors With Enhanced Detection Characteristics
Brock BINKOWSKI - Sauk City WI, US Braeden BUTLER - Madison WI, US Lance P. ENCELL - Fitchburg WI, US Frank FAN - Verona WI, US Brad HOOK - Baraboo WI, US Paul OTTO - Madison WI, US Gediminas VIDUGIRIS - Fitchburg WI, US Susan WIGDAL - Belleville WI, US Kristopher ZIMMERMAN - Madison WI, US
A polynucleotide encoding a biosensor polypeptide comprising a modified circularly-permuted thermostable luciferase and a linker linking the C-terminal portion of the thermostable luciferase to the N-terminal portion of the thermostable luciferase. The modified circularly-permuted thermostable luciferase is modified relative to a parental circularly-permuted thermostable luciferase. The linker contains a sensor region capable of interacting with a target molecule in a cell. The modified circularly-permuted thermostable luciferase has an enhanced response after interaction of the biosensor with the target molecule relative to the parental circularly-permuted thermostable luciferase in the presence of the target molecule. Alternatively, the modified circularly-permuted thermostable luciferase has an enhanced response after interaction of the biosensor with the target molecule relative to the modified circularly-permuted thermostable luciferase in the absence of the target molecule.
Mutant Protease Biosensors With Enhanced Detection Characteristics
Braeden BUTLER - Madison WI, US Lance P. ENCELL - Fitchburg WI, US Frank FAN - Verona WI, US Brad HOOK - Baraboo WI, US Paul OTTO - Madison WI, US Kimberly RISMA - Cincinnati OH, US Gediminas VIDUGIRIS - Fitchburg WI, US Susan WIGDAL - Belleville WI, US Kristopher ZIMMERMAN - Madison WI, US
Assignee:
PROMEGA CORPORATION - Madison WI
International Classification:
C12Q 1/66 C12N 9/02
US Classification:
435 613, 536 232, 4353201, 435 8, 435 618, 435325
Abstract:
A polynucleotide encoding a biosensor polypeptide comprising a modified circularly-permuted thermostable luciferase and a linker linking the C-terminal portion of the thermostable luciferase to the N-terminal portion of the thermostable luciferase. The modified circularly-permuted thermostable luciferase is modified relative to a parental circularly-permuted thermostable luciferase. The linker contains a sensor region capable of interacting with a target molecule in a cell. The modified circularly-permuted thermostable luciferase has an enhanced response after interaction of the biosensor with the target molecule relative to the parental circularly-permuted thermostable luciferase in the presence of the target molecule. Alternatively, the modified circularly-permuted thermostable luciferase has an enhanced response after interaction of the biosensor with the target molecule relative to the modified circularly-permuted thermostable luciferase in the absence of the target molecule.
Synthetic Oplophorus Luciferases With Enhanced Light Output
- Madison WI, US Mary Hall - Waunakee WI, US Paul Otto - Madison WI, US Gediminas Vidugiris - Fitchburg WI, US Keith V. Wood - Mt. Horeb WI, US Monika G. Wood - Mt. Horeb WI, US Kristopher Zimmerman - Madison WI, US
International Classification:
C12N 15/52
Abstract:
A polynucleotide encoding a modified luciferase polypeptide. The modified luciferase polypeptide has at least 60% amino acid sequence identity to a wild-type luciferase and includes at least one amino acid substitution at a position corresponding to an amino acid in a wild-type luciferase of SEQ ID NO: 1. The modified luciferase polypeptide has at least one of enhanced luminescence, enhanced signal stability, and enhanced protein stability relative to the wild-type luciferase.
Synthetic Oplophorus Luciferases With Enhanced Light Output
- Madison WI, US Mary Hall - Waunakee WI, US Paul Otto - Madison WI, US Gediminas Vidugiris - Fitchburg WI, US Keith V. Wood - Mt. Horeb WI, US Monika G. Wood - Mt. Horeb WI, US Kristopher Zimmerman - Madison WI, US
International Classification:
C12Q 1/66 C12N 9/02
Abstract:
A polynucleotide encoding a modified luciferase polypeptide. The modified luciferase polypeptide has at least 60% amino acid sequence identity to a wild-type luciferase and includes at least one amino acid substitution at a position corresponding to an amino acid in a wild-type luciferase of SEQ ID NO:1. The modified luciferase polypeptide has at least one of enhanced luminescence, enhanced signal stability, and enhanced protein stability relative to the wild-type luciferase.
Synthetic Oplophorus Luciferases With Enhanced Light Output
- Madison WI, US Mary Hall - Waunakee WI, US Paul Otto - Madison WI, US Gediminas Vidugiris - Fitchburg WI, US Keith V. Wood - Mt. Horeb WI, US Monika G. Wood - Mt. Horeb WI, US Kristopher Zimmerman - Madison WI, US
International Classification:
C12Q 1/66 C12N 9/02
Abstract:
A polynucleotide encoding a modified luciferase polypeptide. The modified luciferase polypeptide has at least 60% amino acid sequence identity to a wild-type luciferase and includes at least one amino acid substitution at a position corresponding to an amino acid in a wild-type luciferase of SEQ ID NO:1. The modified luciferase polypeptide has at least one of enhanced luminescence, enhanced signal stability, and enhanced protein stability relative to the wild-type luciferase.