Life Technologies Corporation

Molecular Probes, Inc.

Jason Alfred Dallwig

Stephen T Yue

David M Hagen

Gerald Thomas

Ching-Ying Cheung

Scott Rickes

Sean Zimmerman

Joseph Lee

Kathleen Free

Jennifer Hedlind

Laurel Rebecca Stone

Adam Michael Zahner

Kristina Lee Remple

Shih-Jung Huang

Isamu Sato

Matthew Paul Beaudet

Jill Eileen Hendrickson

Stefan Degn

Isarnu Sato

Fluorometer display screen with graphical user interface

Cyanine dye compounds having a substituted methine moiety that are nucleic acid stains, particularly for fluorescent staining of RNA, including compounds having the formula where Ris a C-Calkyl, sulfoalkyl, carboxyalkyl or C-Calkoxy; each Ris independently selected from the group consisting of H, C-Calkyl, C-Calkoxy, fused benzo, trifluoromethyl, amino, sulfo, carboxy and halogen, that is optionally further substituted; at least one of R, R, and Ris an alkyl, aryl, heteroaryl, cyclic, or heterocyclic moiety that is optionally substituted by alkyl, amino, aminoalkyl, carboxy, nitro, or halogen; and the remaining R, Ror Rare hydrogen; X is S, O, or Se; and D is a substituted or unsubstituted pyridinium, quinolinium or benzazolium moiety.

Methine-substituted cyanine dye compounds

Fluorometer display screen

Fluorometer

Cyanine dye compounds having a negatively charged substituent that are nucleic acid stains, particularly for fluorescent staining of DNA, including compounds having the formula wherein W forms one or two fused 5- or 6-membered aromatic rings, &#x3b1; has a value of 0 or 1, n has a value of 0, or 1, X is O, S, or Se, and D is a pyridinium, or quinolinium moiety, provided that the compound has at least one negatively charged substituent.

Cyanine dye compounds

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Eugene, OR, United States of America

Jason Alfred Dallwig