Introduction to Fluorescent Reagents

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10.17721/moca.2021.117-126

The observed effects are explained by the realization of charge and hydrophobic matching in the interaction of surfactants with the fluorescent reagents.

Matching Effects in the Interaction of Ionic Surfactants with Fluorescent Reagents in Micellar Solutions of Triton X-100

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10.1007/s11696-020-01498-3

The influence of charge, hydrophobicity, and spatial characteristics on the analytical signal of cationic and anionic surfactants in their association with fluorescent reagents in aqueous solutions is studied.

Charge, hydrophobic and spatial matching in the association of fluorescent reagents with ionic surfactants in aqueous solutions

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10.1136/ANNRHEUMDIS-2021-EULAR.2150

CS uses a proprietary kit containing a ferrofluid-based reagent, that target CD146 to magnetically capture CECs, and the immunofluorescent reagents to stain the CECs, defined as CD146+, CD105-PE+, DAPI+ and CD45-APC-.

POS0424 DETERMINING CIRCULATING ENDOTHELIAL CELLS USING CELLSEARCH SYSTEM IN SYSTEMIC SCLEROSIS PATIENTS

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10.1007/978-1-0716-1024-4_7

The introduction of fluorescent reagents for protein labeling (difference in-gel electrophoresis or DIGE) has brought substantial improvement in this field.

Differential Proteome Analysis Using 2D-DIGE.

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10.1021/acs.joc.9b01529

Ubiquitin-(Ub) and Ub-like protein-based fluorescent reagents are crucial to explore the activity of Deubiquitinase (DUBs) and to screen its specific inhibitors.

Semi-synthesis of ubiquitin and SUMO-rhodamine-110-glycine through aminolysis of Boc protected thioester counterparts.

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10.1007/978-1-4939-9593-6_14

When used in conjunction with other fluorescent reagents, new labeling technologies, and tagged reporter constructs, these approaches can generate visually appealing and highly informative insights into diverse aspects of vaccinia virus biology.

Visualizing Poxvirus Replication and Recombination Using Live-Cell Imaging.

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What is/are Fluorescent Reagents?

Fluorescent Reagents - The observed effects are explained by the realization of charge and hydrophobic matching in the interaction of surfactants with the fluorescent reagents. [1] The influence of charge, hydrophobicity, and spatial characteristics on the analytical signal of cationic and anionic surfactants in their association with fluorescent reagents in aqueous solutions is studied. [2] CS uses a proprietary kit containing a ferrofluid-based reagent, that target CD146 to magnetically capture CECs, and the immunofluorescent reagents to stain the CECs, defined as CD146+, CD105-PE+, DAPI+ and CD45-APC-. [3] The introduction of fluorescent reagents for protein labeling (difference in-gel electrophoresis or DIGE) has brought substantial improvement in this field. [4] Ubiquitin-(Ub) and Ub-like protein-based fluorescent reagents are crucial to explore the activity of Deubiquitinase (DUBs) and to screen its specific inhibitors. [5] When used in conjunction with other fluorescent reagents, new labeling technologies, and tagged reporter constructs, these approaches can generate visually appealing and highly informative insights into diverse aspects of vaccinia virus biology. [6]