Lawrence Livermore National Security, LLC

University of Texas System

University of New Mexico

Nicholas O Fischer

Craig D Blanchette

Amy Rasley

Matthew A Coleman

Peter W Mason

Todd Peterson

Paul D Hoeprich

Angela C Tooker

Paul Henderson

Elizabeth K Wheeler

Wei He

Martina Felderman

Julie A Lovchik

Heather Ann Enright

Terry Wu

Angela Clare Evans

David Soscia

Michael Triplett

Doris Mailie Lam

Sean Fitzpatrick Gilmore

Kurt I Kamrud

Bolyn Hubby

Heather D Gouvis

Nathaniel S Wang

Nanolipoprotein particles having at least a scaffold protein component and a membrane lipid component and related compositions, methods and systems are described. The membrane lipid component includes at least one or more membrane forming lipids, one or more polymerized lipids and/or one or more polymerizable lipids.

Stable nanolipoprotein particles and related compositions methods and systems

Nanolipoprotein particles comprising at least a scaffold protein component and a membrane lipid component and related complexes, compositions, methods and systems are described, in which the membrane lipid component comprises at least one or more membrane forming lipids and one or more cationic lipids.

Nanolipoprotein particles and related compositions methods and systems for loading RNA

A telodendrimer-nanolipoprotein particle (t-NLP), comprising one or more membrane forming lipids, one or more telodendrimers, and a scaffold protein and amajor outer membrane protein (MOMP) comprising a MOMP hydrophobic region, and related compositions methods and systems.

MOMP telonanoparticles, and related compositions, methods and systems

The present disclosure relates to a biocompatible, in vitro probe system. The probe system may have a substrate and a culture well supported on the substrate. The culture well defines a three-dimensional volume for containing in vitro cultures of electroactive cells. The probe system has at least one probe subsystem supported on the substrate. The probe subsystem has at least one probe having an array of electrodes, with the probe being disposed within the culture well for in vitro electrically communicating with the electroactive cells. The probe subsystem is adapted to be interfaced to an external instrumentation/recording device.

System and method for three-dimensional in vitro flexible microelectrode array

Provided herein are antigenic combinations and related compositions, methods and systems for immunizing a host from an infection caused bybacterium. The antigenic combination comprises an antigenic polysaccharide component from abacterium capable of triggering a humoral immune response in an individual, a protein antigen component from thebacterium capable of triggering a cellular immune response in the individual, and an adjuvant, the antigenicpolysaccharide component, theprotein antigen component and the adjuvant are in a suitable amount to immunize an individual against thebacterium.

Antigenic combinations againstbacteria and related nanolipoprotein particles, compositions, methods and systems

Provided herein are immunostimulatory nanolipoprotein particles and related compositions methods and systems.

Immunostimulatory nanoparticles and related compositions, methods and systems

Functionalized nanolipoprotein particle presenting an anchor substrate compound for binding with a corresponding anchor compound presented on a target molecule, and related compositions methods and systems.

Nanolipoprotein particles and related compositions, methods and systems

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Livermore, CA, United States of America

Nicholas O Fischer