University of California

University of Illinois

The University of Akron

Ming Xiao

Nathan C Gianneschi

Ali Dhinojwala

Paul R Selvin

Pui-Yan Kwok

Matthew Gordon

Ziying Hu

Matthew Shawkey

Ting-Fung Chan

Mathew Gordon

In various embodiments, the present invention is directed to a facile one-pot reverse emulsion process to assemble core-shell nanoparticles (CS-SMNPs) into bright and noniridescent photonic supraballs. In one or more embodiments, the present invention is directed to core-shell nanoparticles having an inner high refractive index (RI) core and an outer low RI shell. In one or more embodiment, the present invention includes core-shell nanoparticles using high RI (˜1.74) melanin cores and low-RI (˜1.45) silica shells. In various embodiments, these nanoparticles may be self-assembled into bright and noniridescent supraballs using a scalable one-pot reverse emulsion process. According to various embodiments of the present invention, it is possible to generate a full spectrum of structural colors with the combination of only two ingredients, synthetic melanin and silica.

Self-assembled melanin particles for color production

In various embodiments, the present invention is directed to a supraparticle for use in producing structural colors comprising a plurality of core/shell nanoparticles having a melanin or synthetic melanin core and a silica shell having a plurality of silanol groups on its outer surface and a poly(ethylene glycol) (PEG) crosslinker. In various embodiments, the structure of these crosslinked supra particles is reinforced by hydrogen bonds formed between the silanol groups on the core-shell nanoparticles and mechanical, solution phase, and dry state stability.

Stabilization of melanin-based supraparticles using polymeric glue

A polynucleotide is barcoded using a method whereby an isolated, individual polynucleotide is immobilized on a solid phase and stretched, targets are labeled using target-specific hybridization probes, and an individual label of an unamplified probe at each of the labeled targets is optically detected. The order of the labels is determined to form a barcode representation of the polynucleotide wherein the targets and their relative positions are represented.

Polynucleotide barcoding

Improved methods of genetic haplotyping and DNA sequencing and mapping, including methods for making amplified ssDNA, methods for allele determination, and a DNA barcoding strategy based on direct imaging of individual DNA molecules and localization of multiple sequence motifs or polymorphic sites on a single DNA molecule.

Methods for determining genetic haplotypes and DNA mapping

Growing community of inventors

Pacifica, CA, United States of America

Ming Xiao