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:
Jul. 28, 2015

Filed:

Feb. 24, 2014
Applicant:

Applied Biosystems, Llc, Carlsbad, CA (US);

Inventors:

Joe Y. Lam, Castro Valley, CA (US);

Steven Menchen, Fremont, CA (US);

Ruiming Zou, Foster City, CA (US);

Scott Benson, Alameda, CA (US);

Assignee:

Applied Biosystems, LLC, Carlsbad, CA (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C09B 62/002 (2006.01); C09B 57/00 (2006.01); C09B 13/00 (2006.01); C07D 311/82 (2006.01); C07D 491/14 (2006.01); C09B 11/06 (2006.01); C09B 11/24 (2006.01); C09B 11/12 (2006.01); C09B 11/26 (2006.01);
U.S. Cl.
CPC ...
C09B 13/00 (2013.01); C07D 311/82 (2013.01); C07D 491/14 (2013.01); C09B 11/06 (2013.01); C09B 11/12 (2013.01); C09B 11/24 (2013.01); C09B 11/26 (2013.01); C09B 57/00 (2013.01); C09B 62/0025 (2013.01);
Abstract

Fluorescent phenyl xanthene dyes are described that comprise any fluorescein, rhodamine or rhodol comprising a particular C9 phenyl ring. One or both of the ortho groups on the lower C9 phenyl ring is ortho substituted with a group selected from alkyl, heteroalkyl, alkoxy, halo, haloalkyl, amino, mercapto, alkylthio, cyano, isocyano, cyanato, mercaptocyanato, nitroso, nitro, azido, sulfeno, sulfinyl, and sulfino. In one embodiment, halo and/or hydroxy groups are used. Optimal dyes contain a lower C9 phenyl ring in which both ortho groups are the same and the lower ring exhibits some form a symmetry relative to an imaginary axis running from the phenyl rings point of attachment to the remainder of the xanthene dye through a point para to the point of attachment. The phenyl xanthene dyes may be activated. Furthermore, the phenyl xanthene dyes may be conjugated to one or more substances including other dyes. The phenyl xanthene dyes are useful for a number of purposes, including labels for use in automated DNA sequencing as well the formation of fluorescent 'bar codes' for polymeric particles used in the multiplexed analysis of analytes.


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