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1.
Patterns (N Y) ; 3(9): 100584, 2022 Sep 09.
Article in English | MEDLINE | ID: mdl-36124300

ABSTRACT

This article systematically investigates the technology licensing by Stanford University. We analyzed all the inventions marketed by Stanford's Office of Technology Licensing (OTL) between 1970 to 2020, with 4,512 inventions from 6,557 inventors. We quantified how the innovation landscape at Stanford changed over time and examined factors that correlate with commercial success. We found that the most profitable inventions are predominantly licensed by inventors' own startups, inventions have involved larger teams over time, and the proportion of female inventors has tripled over the past 25 years. We also identified linguistic features in how the inventors and OTL describe the inventions that significantly correlate with the invention's future revenue. Interestingly, inventions with more adjectives in their abstracts have worse net income. Our study opens up a new perspective for analyzing the translation of research into practice and commercialization using large-scale computational and linguistics analysis.

2.
Proc Natl Acad Sci U S A ; 101(26): 9517-22, 2004 Jun 29.
Article in English | MEDLINE | ID: mdl-15210951

ABSTRACT

We report the fabrication of enthalpy arrays and their use to detect molecular interactions, including protein-ligand binding, enzymatic turnover, and mitochondrial respiration. Enthalpy arrays provide a universal assay methodology with no need for specific assay development such as fluorescent labeling or immobilization of reagents, which can adversely affect the interaction. Microscale technology enables the fabrication of 96-detector enthalpy arrays on large substrates. The reduction in scale results in large decreases in both the sample quantity and the measurement time compared with conventional microcalorimetry. We demonstrate the utility of the enthalpy arrays by showing measurements for two protein-ligand binding interactions (RNase A + cytidine 2'-monophosphate and streptavidin + biotin), phosphorylation of glucose by hexokinase, and respiration of mitochondria in the presence of 2,4-dinitrophenol uncoupler.


Subject(s)
Biotin/metabolism , Cytidine Monophosphate/metabolism , Protein Array Analysis/methods , Ribonuclease, Pancreatic/metabolism , Streptavidin/metabolism , 2,4-Dinitrophenol/pharmacology , Animals , Biotin/chemistry , Cattle , Cell Respiration/drug effects , Cytidine Monophosphate/chemistry , Equipment Design , Glucose/metabolism , Hexokinase/metabolism , Ligands , Mitochondria, Heart/drug effects , Mitochondria, Heart/metabolism , Phosphorylation , Protein Array Analysis/instrumentation , Protein Binding , Ribonuclease, Pancreatic/chemistry , Streptavidin/chemistry , Thermodynamics
3.
J Biomol Screen ; 9(2): 85-94, 2004 Mar.
Article in English | MEDLINE | ID: mdl-15006131

ABSTRACT

The authors have constructed an array of 12 piezoelectric ejectors for printing biological materials. A single-ejector footprint is 8 mm in diameter, standing 4 mm high with 2 reservoirs totaling 76 micro L. These ejectors have been tested by dispensing various fluids in several environmental conditions. Reliable drop ejection can be expected in both humidity-controlled and ambient environments over extended periods of time and in hot and cold room temperatures. In a prototype system, 12 ejectors are arranged in a rack, together with an X - Y stage, to allow printing any pattern desired. Printed arrays of features are created with a biological solution containing bovine serum albumin conjugated oligonucleotides, dye, and salty buffer. This ejector system is designed for the ultra-high-throughput generation of arrays on a variety of surfaces. These single or racked ejectors could be used as long-term storage vessels for materials such as small molecules, nucleic acids, proteins, or cell libraries, which would allow for efficient preprogrammed selection of individual clones and greatly reduce the chance of cross-contamination and loss due to transfer. A new generation of design ideas includes plastic injection molded ejectors that are inexpensive and disposable and handheld personal pipettes for liquid transfer in the nanoliter regime.


Subject(s)
Oligonucleotide Array Sequence Analysis , Printing/instrumentation , Cell Line , Computer-Aided Design , DNA/analysis , Equipment Design , Humans , Ink , Microchemistry/instrumentation , Microchemistry/methods , Miniaturization , Models, Biological , Oligonucleotide Array Sequence Analysis/instrumentation , Oligonucleotide Array Sequence Analysis/methods
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