Tomasz J Bakowski

20110059556, Mar 10, 2011

Sep 3, 2010

12/875914

Helmut Strey - Stony Brook NY, US
Robert Kimmerling - Shirley NY, US
Tomasz Bakowski - Levittown NY, US

The Research Foundation of State University of New York - Albany NY

G01N 33/543
B01L 3/00
C12M 1/00

436518, 422503, 4352872

The compositions and methods described herein are designed to introduce functionalized microparticles into droplets that can be manipulated in microfluidic devices by fields, including electric (dielectrophoretic) or magnetic fields, and extracted by splitting a droplet to separate the portion of the droplet that contains the majority of the microparticles from the part that is largely devoid of the microparticles. Within the device, channels are variously configured at Y- or T junctions that facilitate continuous, serial isolation and dilution of analytes in solution. The devices can be limited in the sense that they can be designed to output purified analytes that are then further analyzed in separate machines or they can include additional channels through which purified analytes can be further processed and analyzed.

20180250678, Sep 6, 2018

Feb 28, 2018

15/908453

- Albany NY, US
Robert Kimmerling - Shirley NY, US
Tomasz Bakowski - Levittown NY, US

B01L 3/00
C12N 15/10
G01N 33/543
C12Q 1/686

The compositions and methods described herein are designed to introduce functionalized microparticles into droplets that can be manipulated in microfluidic devices by fields, including electric (dielectrophoretic) or magnetic fields, and extracted by splitting a droplet to separate the portion of the droplet that contains the majority of the microparticles from the part that is largely devoid of the microparticles. Within the device, channels are variously configured at Y- or T junctions that facilitate continuous, serial isolation and dilution of analytes in solution. The devices can be limited in the sense that they can be designed to output purified analytes that are then further analyzed in separate machines or they can include additional channels through which purified analytes can be further processed and analyzed.

20170182495, Jun 29, 2017

Mar 13, 2017

15/457459

- Albany NY, US
Robert Kimmerling - Shirley NY, US
Tomasz Bakowski - Levittown NY, US

B01L 3/00
G01N 33/543
C12N 15/10
C12Q 1/68

The compositions and methods described herein are designed to introduce functionalized microparticles into droplets that can be manipulated in microfluidic devices by fields, including electric (dielectrophoretic) or magnetic fields, and extracted by splitting a droplet to separate the portion of the droplet that contains the majority of the microparticles from the part that is largely devoid of the microparticles. Within the device, channels are variously configured at Y- or T junctions that facilitate continuous, serial isolation and dilution of analytes in solution. The devices can be limited in the sense that they can be designed to output purified analytes that are then further analyzed in separate machines or they can include additional channels through which purified analytes can be further processed and analyzed.