NIR dye-1 is a near-infrared (NIR) fluorescent dye which has absorption and emission in the NIR region while retaining an optically tunable hydroxyl group.
BODIPY-TS (also known as Thiol-green 2) is a highly efficient thiol-specific turn-on probe with a fast response. It incorporates a thiosulfonate scaffold as its thiol recognition unit. BODIPY-TS displays excellent selectivity, low detection limit, and quantitative reactivity towards thiols. Moreover, it exhibits low toxicity. Notably, BODIPY-TS exhibits excitation at 490 nm and emission at 515 nm.
NFQ1 作为一种非荧光淬灭剂(吸收波长:474 nm),广泛应用于新型 One Sample Fluorescence Resonance Energy Transfer (OS-FRET) 方法中。该方法通过测量同一样品中未被淬灭的供体发射,利用 NFQ1 的宽广吸收光谱,确保其作为多种供体的有效暗接受剂。
BDP 630 650 maleimide, a fluorophore compatible with the Cyanine5 channel, is valuable for fluorescence lifetime measurements due to its extended excited state lifetime [1].
5MP-Fluorescein (compound 3e), a fluorescein dye derived from 5-Methylene pyrrolone (5MP), exemplifies a bioconjugation tool that is both highly thiol-specific and can be removed without a trace [1].
Naph-EA-mal (Thiol-green 1) is a highly efficient and quick-responding thiol fluorescence probe specifically designed for protein labeling and bioimaging applications. This compound offers a rapid detection method and exhibits ultrafast turn-on fluorescence upon interaction with thiols. Naph-EA-mal (Thiol-green 1) enables the detection of thiols in live cells, facilitates the labeling of protein thiols, enables quantification of total thiol concentration in cell lysate, and allows for the determination of reversible protein thiol oxidation in fixed cells. It possesses an excitation wavelength of 488 nM and an emission wavelength of 540 nM.
N-(3-Fluoranthyl)maleimide, a thiol fluorescent probe with a lifetime of 20 nsec, has a maximum excitation wavelength of 370 nm and is suitable for studying time-dependent processes of biopolymers [1].
NIR-Thiol dinitrobenzenesulfonate has both absorption and emission in the NIR region. It is capable of imaging endogenously produced thiol in living cells and mice.
Acrylodan, when subjected to thiol reactions, exhibits sensitivity to the dipolarity and dynamics of its surrounding binding pocket, specifically those surrounding Cys 34.