Familiar with and have utilized aseptic ... • Experience in cell culturing and passaging • Knowledge and understanding of biochemic... • western blot • and PCR • Experience using a light microscope and ... • Background in data manipulation • statistical analysis • and graphical representation • Ability to organize and maintain lab sup... • Extensive experience with Microsoft Excel • Word • and PowerPoint • Knowledge of good clinical practices • Able to design and follow study protocol • Clinical experience including knowledge ... • Three years leadership experience on exe...
The present invention provides a method for the in vitro selection of signaling aptamers comprising the steps of synthesizing a DNA pool, the DNA having a random insert of nucleotides of a specific skewed mole ratio; amplifying the DNA pool; transcribing an RNA pool from the amplified DNA using a fluorescently labeled nucleotide; applying the fluorescently labeled RNA pool to an affinity column to remove the high-affinity fluorescent RNA molecules from the fluorescently labeled RNA pool; obtaining a cDNA pool from the high-affinity fluorescent RNA molecules; repeating the amplification and selection steps on the fluorescent RNA molecules and cloning the fluorescent RNA molecules to yield signaling aptamers. Signaling aptamers comprising DNA molecules are also selected for. Also provided is a signaling aptamer that transduces the conformational change upon binding a ligand to a change in fluorescence intensity of the signaling aptamer.
Methods For Recombinatorial Nucleic Acid Synthesis
This invention pertains to a method for generating a pool of nucleic acid fragments useful for in vitro recombination and the creation of novel DNA sequences that encode desirable proteins or enzymes. The invention provides a defined mixture of nucleic acids and methods for use in the synthesis, mutagenesis, and recombination of nucleic acids. Nucleic acids may be synthesized by creating a nucleic acid extension ladder, annealing the extension ladder to template nucleic acids, and further extending the ladder of nucleic acids. The invention also relates to methods for performing repeated cycles of synthesis for the purpose of mutagenesis or recombination, methods for producing mutant peptides and proteins from the mutagenized or recombined nucleic acids, and methods for selecting a peptide, polypeptide or protein having altered biological activities.
Selection Method For Cell Internalizing Nucleic Acids
Andrew D. Ellington - Austin TX, US Matthew Levy - Larchmont NY, US Amy Yan - Larchmont NY, US Ted Chitai Chu - Palo Alto CA, US
Assignee:
Board of Regents, The University of Texas System - Austin TX
International Classification:
C12Q 1/68 C12N 5/00 C12N 5/02 C07H 21/02
US Classification:
435 61, 435325, 536 231
Abstract:
The present invention includes compositions and methods for contacting one or more cells with a random RNA-containing library, treating the contacted cells and with a denaturing agent or digestion with one or more nucleases, and extracting from the cells one or more internalized nucleic acids resistant to the nucleases or denaturants.
Signaling Aptamers That Transduce Molecular Recognition To A Differential Signal
The present invention provides a method of transducing the conformational change undergone by a signaling aptamer upon binding a ligand to a differential signal generated by a reporter molecule. Also provided is a method of detecting and quantitating a ligand in solution using an aptamer conjugated to a fluorescent dye (signaling aptamer) to bind to the ligand and measuring the resultant optical signal generated.
Andrew Ellington - Austin TX, US Jay Hesselberth - Austin TX, US Kristin Marshall - Cambridge MA, US Michael Robertson - Austin TX, US Letha Sooter - Austin TX, US Eric Davidson - Austin TX, US J. Cox - Austin TX, US Timothy Reidel - Austin TX, US
Compositions and methods are provided to make, isolate, characterize and use regulatable, catalytically active nucleic acids (RCANA). RCANA may be used for regulating gene expression and in assays to detect the presence of ligands or to detect activation by an effector of an RCANA bound to a solid support such as a chip or multi-well plate. Also disclosed are compositions and methods for automating the selection procedures of the present invention.
Konstantin Sokolov - Austin TX, US Brian Korgel - Round Rock TX, US Andrew Ellington - Austin TX, US
International Classification:
G01N033/543
US Classification:
436/518000
Abstract:
Methods and apparatuses for detecting a condition of a sample (including cervical cancers and pre-cancers) through reflectance and/or fluorescence imaging. A sample is obtained. One or more metallic nanoparticles and/or one or more quantum dots are obtained. The one or more metallic nanoparticles and/or one or more quantum dots are coupled to one or more biomarkers of the sample that are associated with the condition. A reflectance and/or fluorescence image of the sample is then taken. The image(s) exhibit characteristic optical scattering from the one or more metallic nanoparticles and/or characteristic fluorescence excitation from the one or more quantum dots to signal the presence of the one or more biomarkers. In this way, the condition can be readily screened or diagnosed.
Andrew Ellington - Austin TX, US Sulay Jhaveri - Alexandria VA, US Manjula Rajendran - Austin TX, US
Assignee:
Research Development Foundation
International Classification:
C12Q001/68 C07H021/02
US Classification:
435/006000, 536/023100
Abstract:
The present invention provides a method for the in vitro selection of signaling aptamers comprising the steps of synthesizing a DNA pool, the DNA having a random insert of nucleotides of a specific skewed mole ratio; amplifying the DNA pool; transcribing an RNA pool from the amplified DNA using a fluorescently labeled nucleotide; applying the fluorescently labeled RNA pool to an affinity column to remove the high-affinity fluorescent RNA molecules from the fluorescently labeled RNA pool; obtaining a cDNA pool from the high-affinity fluorescent RNA molecules; repeating the amplification and selection steps on the fluorescent RNA molecules and cloning the fluorescent RNA molecules to yield signaling aptamers. Signaling aptamers comprising DNA molecules are also selected for. Also provided is a signaling aptamer that transduces the conformational change upon binding a ligand to a change in fluorescence intensity of the signaling aptamer.
Andrew Ellington - Austin TX, US Jay Hesselberth - Seattle WA, US Kristin Thompson - Arlington MA, US Michael Robertson - Santa Cruz CA, US Letha Sooter - Austin TX, US Eric Davidson - Houston TX, US J. Cox - Austin TX, US Timothy Riedel - New Braunfels TX, US Charles Wilson - Concord MA, US Sharon Cload - Cambridge MA, US Anthony Keefe - Cambridge MA, US
International Classification:
C07H021/02 C12N015/85
US Classification:
435/455000, 536/023100
Abstract:
Compositions and methods are provided to make, isolate, characterize and use regulatable, catalytically active nucleic acids (RCANA). The present invention is directed to RCANA that transduce molecular recognition into catalysis. Also, RCANAs according to the invention can be used as regulatory elements to control the expression of one or more genes in a metabolic pathway. RCANAs can also be used as regulated selectable markers to create a selective pressure favoring (or disfavoring) production of a targeted bioproduct.
Feb 2013 to 2000 Emergency Medical TechnicianMammalian Cell Culturing. Dr. David Basile
Sep 2013 to Jun 2014 Research ExperienceIndiana University Health North Hospital
Sep 2012 to Dec 2013 Emergency Medical TechnicianKappa Delta Rho, Nu Chapter Bloomington, IN Dec 2008 to Dec 2012 Executive BoardRed Lobster
Jan 2012 to Aug 2012 ServerKappa Delta Rho, Nu Chapter
Jan 2011 to Dec 2011 PresidentUniversity Information Technology Services
Aug 2010 to Aug 2011 Technology Center ConsultantKappa Delta Rho, Nu Chapter
Jan 2010 to Dec 2010 Vice President of EducationKappa Delta Rho, Nu Chapter Bloomington, IN Jan 2009 to Dec 2009 Vice President of Risk Mangement
Education:
Indiana University School of Medicine Aug 2013 M.S. in PhysiologyIndiana University Bloomington Aug 2008 to Dec 2012 B.S. in Biology
Skills:
Familiar with and have utilized aseptic techniques both in laboratory and clinical settings, Experience in cell culturing and passaging, Knowledge and understanding of biochemical assays including but not limited to ELISA, western blot, and PCR, Experience using a light microscope and understanding of other microscope techniques such as FRET, Background in data manipulation, statistical analysis, and graphical representation, Ability to organize and maintain lab supplies and equipment, Extensive experience with Microsoft Excel, Word, and PowerPoint, Knowledge of good clinical practices, Able to design and follow study protocol, Clinical experience including knowledge of clinical tests and procedures, Three years leadership experience on executive board of Kappa Delta Rho
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Company / Classification
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3925 W Braker Ln, Austin, TX 78759 512-232-3041
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Andy Ellington (1993-1997), Doris Willson (1958-1964), Robert Cook (1960-1961), John Cox (1983-1985), Julie Holt (1976-1980), Elizabeth Grosso (1994-1998)
News
Plastic-eating Enzyme Could Eliminate Billions of Tons of Landfill Waste - UT News
This work really demonstrates the power of bringing together different disciplines, from synthetic biology to chemical engineering to artificial intelligence, said Andrew Ellington, professor in the Center for Systems and Synthetic Biology whose team led the development of the machine learning mod
Date: Apr 27, 2022
Category: Business
Source: Google
Cells with lab-made DNA produce a new kind of protein, a 'holy grail' for synthetic biology
It's wave front stuff, this is the edge of science, said Andrew Ellington, a biochemist at the University of Texas at Austin who was not involved in the research. We are better learning how to engineer living systems.