The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Nov. 18, 2008

Filed:

Dec. 11, 2003
Applicants:

Hou-pu Chou, Sunnyvale, CA (US);

Antoine Daridon, Belmont, CA (US);

Kevin Farrell, San Francisco, CA (US);

Brian Fowler, Foster City, CA (US);

Yish-hann Liau, San Jose, CA (US);

Ian D. Manger, San Francisco, CA (US);

Hany Ramez Nassef, San Mateo, CA (US);

William Throndset, San Francisco, CA (US);

Inventors:

Hou-Pu Chou, Sunnyvale, CA (US);

Antoine Daridon, Belmont, CA (US);

Kevin Farrell, San Francisco, CA (US);

Brian Fowler, Foster City, CA (US);

Yish-Hann Liau, San Jose, CA (US);

Ian D. Manger, San Francisco, CA (US);

Hany Ramez Nassef, San Mateo, CA (US);

William Throndset, San Francisco, CA (US);

Assignee:

Fluidigm Corporation, San Francisco, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
G01N 35/00 (2006.01); G01N 33/48 (2006.01); G01N 1/10 (2006.01); G01N 15/06 (2006.01); G01N 33/00 (2006.01);
U.S. Cl.
CPC ...
Abstract

The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and/or detection of particles, such as cells and/or beads. The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and/or analysis of particles, such as cells, viruses, organelles, beads, and/or vesicles. The invention also provides microfluidic mechanisms for carrying out these manipulations and analyses. These mechanisms may enable controlled input, movement/positioning, retention/localization, treatment, measurement, release, and/or output of particles. Furthermore, these mechanisms may be combined in any suitable order and/or employed for any suitable number of times within a system. Accordingly, these combinations may allow particles to be sorted, cultured, mixed, treated, and/or assayed, among others, as single particles, mixed groups of particles, arrays of particles, heterogeneous particle sets, and/or homogeneous particle sets, among others, in series and/or in parallel. In addition, these combinations may enable microfluidic systems to be reused. Furthermore, these combinations may allow the response of particles to treatment to be measured on a shorter time scale than was previously possible. Therefore, systems of the invention may allow a broad range of cell and particle assays, such as drug screens, cell characterizations, research studies, and/or clinical analyses, among others, to be scaled down to microfluidic size. Such scaled-down assays may use less sample and reagent, may be less labor intensive, and/or may be more informative than comparable macrofluidic assays.


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