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Sf7 am fluorescent probe

Manufactured by Merck Group

The SF7-AM fluorescent probe is a chemical compound used in research applications. It functions as a fluorescent indicator, detecting and measuring specific analytes or parameters within a sample. The core purpose of this product is to facilitate fluorescence-based analysis and monitoring, without further interpretation of its intended use.

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3 protocols using sf7 am fluorescent probe

1

Fluorescent Quantification of Protein Persulfidation

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Free H2S was measured in cells using the SF7-AM fluorescent probe [30 (link)] (Sigma-Aldrich). The probe was dissolved in anhydrous DMF at 5 mM and used at 5 μM in serum-free RPMI. Live-cell image acquisition was performed using a Nikon Ti2 spinning disk confocal microscope. Global protein persulfidation was assessed on VSMC grown on glass coverslips as previously described [9 (link)]. Cells were incubated for 20 min with 1 mM 4-Chloro-7-nitrobenzofurazan (NBF-Cl, Sigma-Aldrich) diluted in PBS. Then, cells were washed with PBS and fixed for 10 min in ice-cold methanol. Coverslips were rehydrated in PBS and incubated with 1mM NBF-Cl for 1 h at 37 °C. In parallel, a Daz2-Cy5.5 solution was prepared by mixing 1mM Daz-2, 1 mM alkyne Cy5.5, 2 mM copper(II)-TBTA, 4mM ascorbic acid and incubating overnight at RT, followed by quenching for 1h with 20mM EDTA. Fixed cells were further incubated at 37 °C for 1h in the Daz2-Cy5.5 solution. Finally, coverslips were washed 3 times in methanol and 2 times in PBS, mounted in Vectashield mounting medium with DAPI, and visualized with a 90i Nikon fluorescence microscope. Persulfidation was measured as the ratio of Daz2-Cy5.5 over NBF-Cl signal per cell by two independent experimenter blinded to the conditions using the Fiji (ImageJ 1.53t) software.
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2

Quantifying Free H2S and Protein Persulfidation

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Free H2S was measured in cells using the SF7-AM fluorescent probe (29 (link)) (Sigma-Aldrich). The probe was dissolved in anhydrous DMF at 5 mM and used at 5 μM in serum-free EBM-2.
Global protein persulfidation was assessed on HUVEC grown on glass coverslips as previously described (23 (link)). Cells were incubated for 20 mins with 1 mM 4-Chloro-7-nitrobenzofurazan (NBF-Cl, Sigma) diluted in PBS. Then, cells were washed with PBS and fixed for 10 mins in ice-cold methanol. Coverslips were rehydrated in PBS, and incubated with 1 mM NBF-Cl for 1 h at 37°C. Cells were further incubated at 37°C for 1 h in Daz2-Cy5.5 solution prepared as previously described (23 (link)). Finally, coverslips were washed three times in methanol and two times in PBS, mounted in Vectashield mounting medium with DAPI, and visualized with a 90i Nikon fluorescence microscope.
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3

Quantifying Cellular Free Sulfide

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Free sulfide was measured in cells using the SF7-AM fluorescent probe [28 (link)] (Sigma-Aldrich cat: 748110). The probe was dissolved in anhydrous DMF at 5 mM. 105 cells per well were plated in a 96 well plate. After 24 h, SF7-AM (5 μM) was added to VSMCs or HUVECs, and fluorescence intensity (λex = 495 nm; λem = 520 nm) was measured continuously in a Synergy Mx fluorescent plate reader at 37 °C before and after addition of various donors as indicated. Linear regressions of the SF7-AM fluorescent signal were calculated during the linear part of the curves generated to measure the H2S release rate.
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