Atlantic Capital Group Raleigh, NC Mar 2006 to Jun 2008 Owner, Broker & Contractor - BudgetNorth Nations Mortgage Raleigh, NC May 1998 to Aug 2006 dba Wise Choice Mortgage
Education:
Shaw University Raleigh, NC May 1989 Bachelor of Science in Business Management
Sample Collection Devices And Methods Using Markers And The Use Of Such Markers As Controls In Sample Validation, Laboratory Evaluation And/Or Accreditation
The invention is directed to a device suitable for marking a collected sample, comprising collecting means for collecting the sample and at least one detectable marker which is associated with at least a portion of the collecting means, wherein the at least one detectable marker is contractable with the sample upon collection of the sample to mark the collected sample upon contact of the sample with the at least a portion of the collecting means having the at least one detectable marker associated therewith, and wherein the at least one detectable marker is other than a component which is present in the sample before collection and is inert to any component present in the sample before collection. Kits containing the device, methods for marking samples using the device, methods for determining the integrity of a marked sample, and use of the markers for the testing of laboratories and/or laboratory personnel for certification, proficiency testing or accreditation purposes are also provided.
Methods And Compositions For Determining The Purity Of Chemically Synthesized Nucleic Acids
Paul F. Agris - Raleigh NC, US Christopher D. J. Pearce - Surrey, GB Lloyd G. Mitchell - Durham NC, US
Assignee:
North Carolina State University - Raleigh NC
International Classification:
G01N 33/53
US Classification:
435 71, 435 6
Abstract:
This application describes an antibody that specifically binds to a synthetic oligomer (e. g. , an oligonucleotide or oligopeptide) having a organic protecting group covalently bound thereto, which antibody does not bind to that synthetic oligomer when the organic protecting group is not covalently bound thereto. Methods of making and using such antibodies are also disclosed, along with cells for making such antibodies and articles carrying immobilized oligomers that can be used in assay procedures with such antibodies.
Methods And Compositions For Determining The Purity Of Chemically Synthesized Nucleic Acids
Paul F. Agris - Raleigh NC, US Christopher D. J. Pearce - Surrey, GB Lloyd G. Mitchell - Durham NC, US
Assignee:
North Carolina State University - Raleigh NC
International Classification:
G01N 33/53
US Classification:
435 71, 435 72, 435518
Abstract:
This application describes an antibody that specifically binds to a synthetic oligomer (e. g. , an oligonucleotide or oligopeptide) having a organic protecting group covalently bound thereto, which antibody does not bind to that synthetic oligomer when the organic protecting group is not covalently bound thereto. Methods of making and using such antibodies are also disclosed, along with cells for making such antibodies and articles carrying immobilized oligomers that can be used in assay procedures with such antibodies.
Methods And Compositions For Determining The Purity Of Chemically Synthesized Nucleic Acids
Paul F. Agris - Raleigh NC, US Christopher D. J. Pearce - Surrey, GB Lloyd G. Mitchell - Durham NC, US
Assignee:
North Carolina State University - Raleigh NC
International Classification:
G01N 33/53
US Classification:
435 71, 436518
Abstract:
This application describes an antibody that specifically binds to a synthetic oligomer (e. g. , an oligonucleotide or oligopeptide) having a organic protecting group covalently bound thereto, which antibody does not bind to that synthetic oligomer when the organic protecting group is not covalently bound thereto. Methods of making and using such antibodies are also disclosed, along with cells for making such antibodies and articles carrying immobilized oligomers that can be used in assay procedures with such antibodies.
Methods And Compositions For Use In Spliceosome Mediated Rna Trans-Splicing
Lloyd Mitchell - Durham NC, US Mariano Garcia-Blanco - Durham NC, US Madaiah Puttaraju - Durham NC, US S. Mansfield - Durham NC, US
International Classification:
C12P021/02 C12N005/06 C07H021/04
US Classification:
435/325000, 435/320100, 536/023100
Abstract:
The molecules and methods of the present invention provide a means for in vivo production of a trans-spliced molecule in a selected subset of cells. The pre-trans-splicing molecules of the invention are substrates for a trans-splicing reaction between the pre-trans-splicing molecules and a pre-mRNA which is uniquely expressed in the specific target cells. The in vivo trans-splicing reaction provides a novel mRNA which is functional as mRNA or encodes a protein to be expressed in the target cells. The expression product of the mRNA is a protein of therapeutic value to the cell or host organism a toxin which causes killing of the specific cells or a novel protein not normally present in such cells. The invention further provides PTMs that have been genetically engineered for the identification of exon/intron boundaries of pre-mRNA molecules using an exon tagging method. The PTMs of the invention can also be designed to result in the production of chimeric RNA encoding for peptide affinity purification tags which can be used to purify and identify proteins expressed in a specific cell type.
Methods And Compositions For Use In Spliceosome Mediated Rna Trans-Splicing
Lloyd Mitchell - Durham NC, US Mariano Garcia-Blanco - Durham NC, US Carl Baker - Potomac MD, US Madaiah Puttaraju - Durham NC, US
International Classification:
C12P021/02 C12N005/06 C12N015/86
US Classification:
435/069100, 435/325000, 435/456000
Abstract:
The molecules and methods of the present invention provide a means for in vivo production of a trans-spliced molecule in a selected subset of cells. The pre-trans-splicing molecules of the invention are substrates for a trans-splicing reaction between the pre-trans-splicing molecules and a pre-mRNA which is uniquely expressed in the specific target cells. The in vivo trans-splicing reaction provides a novel mRNA which is functional as mRNA or encodes a protein to be expressed in the target cells. The expression product of the mRNA is a protein of therapeutic value to the cell or host organism a toxin which causes killing of the specific cells or a novel protein not normally present in such cells. The invention further provides PTMs that have been genetically engineered for the identification of exon/intron boundaries of pre-mRNA molecules using an exon tagging method. The PTMs of the invention can also be designed to result in the production of chimeric RNA encoding for peptide affinity purification tags which can be used to purify and identify proteins expressed in a specific cell type.
Methods And Compositions For Use In Spliceosome Mediated Rna Trans-Splicing
The molecules and methods of the present invention provide a means for in vivo production of a trans-spliced molecule in a selected subset of cells. The pre-trans-splicing molecules of the invention are substrates for a trans-splicing reaction between the pre-trans-splicing molecules and a pre-mRNA which is uniquely expressed in the specific target cells. The in vivo trans-splicing reaction provides a novel mRNA which is functional as mRNA or encodes a protein to be expressed in the target cells. The expression product of the mRNA is a protein of therapeutic value to the cell or host organism a toxin which causes killing of the specific cells or a novel protein not normally present in such cells. The invention further provides PTMs that have been genetically engineered for the identification of exon/intron boundaries of pre-mRNA molecules using an exon tagging method. The PTMs of the invention can also be designed to result in the production of chimeric RNA encoding for peptide affinity purification tags which can be used to purify and identify proteins expressed in a specific cell type.
Methods And Compositions For Use In Spliceosome Mediated Rna Trans-Splicing
S. Mansfield - Durham NC, US Lloyd Mitchell - Durham NC, US Mariano Garcia-Blanco - Durham NC, US Christopher Walsh - Chapel Hill NC, US Hengjun Chao - Carboro NC, US
International Classification:
A61K038/37 C12Q001/68 C12N005/06 C07K014/755
US Classification:
514/012000, 435/325000, 435/006000, 530/383000
Abstract:
The molecules and methods of the present invention provide a means for in vivo production of a trans-spliced molecule in a selected subset of cells. The pre-trans-splicing molecules of the invention are substrates for a trans-splicing reaction between the pre-trans-splicing molecules and a pre-mRNA which is uniquely expressed in the specific target cells. The in vivo trans-splicing reaction provides a novel mRNA which is functional as mRNA or encodes a protein to be expressed in the target cells. The expression product of the mRNA is a protein of therapeutic value to the cell or host organism a toxin which causes killing of the specific cells or a novel protein not normally present in such cells. The invention further provides PTMs that have been genetically engineered for the identification of exon/intron boundaries of pre-mRNA molecules using an exon tagging method. The PTMs of the invention can also be designed to result in the production of chimeric RNA encoding for peptide affinity purification tags which can be used to purify and identify proteins expressed in a specific cell type.
Police at the scene of a double shooting in Ridgewood, Queens on May 9, 2022.Photo by Lloyd Mitchell Police cordoned off the block of Fresh Pond Road during a shooting investigation on May 9, 2022.Photo by Lloyd Mitchell