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Sds detergent

Manufactured by Thermo Fisher Scientific
Sourced in United States

SDS (Sodium Dodecyl Sulfate) is a detergent commonly used in laboratory applications. It functions as an anionic surfactant, capable of solubilizing and denaturing proteins. SDS is often used in various analytical techniques, such as SDS-PAGE, to separate and study proteins.

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2 protocols using sds detergent

1

Polyacrylamide Gel Deformation Tracking

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For tracking deformation in polyacrylamide (PAA) gels (Polio and Smith, 2014 (link); Ray et al., 2017 (link)) during traction force microscopy (TFM) analysis, we modified patterned PAA platforms by adding well-ultrasonicated 0.2mm fluorescent nanobeads (Polysciences) into PAA solutions (1:1000 dilution) before gel polymerization. ‘‘Before’’ and ‘‘after’’ cell removal images of the PAA micropatterns were taken with live confocal laser scanning at the interface planes between cells and the adhesion ligands patterns. Cell removal was performed by adding SDS detergent (Fisher Bioreagents, USA) to the final concentration of 0.5% (w/vol). Live cell imaging was performed in a microclimate-controlled stage top incubator (Tokai Hit, Japan) at 37° C in 5% CO2. Bead displacements and corresponding traction forces fields were calculated using an iterative particle image velocimetry (PIV) algorithm and an unconstrained Fourier transform traction cytometry algorithm, respectively (ImageJ plugins)(Tseng et al., 2012 (link)).
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2

Polyacrylamide Gel Deformation Tracking

Check if the same lab product or an alternative is used in the 5 most similar protocols
For tracking deformation in polyacrylamide (PAA) gels (Polio and Smith, 2014 (link); Ray et al., 2017 (link)) during traction force microscopy (TFM) analysis, we modified patterned PAA platforms by adding well-ultrasonicated 0.2mm fluorescent nanobeads (Polysciences) into PAA solutions (1:1000 dilution) before gel polymerization. ‘‘Before’’ and ‘‘after’’ cell removal images of the PAA micropatterns were taken with live confocal laser scanning at the interface planes between cells and the adhesion ligands patterns. Cell removal was performed by adding SDS detergent (Fisher Bioreagents, USA) to the final concentration of 0.5% (w/vol). Live cell imaging was performed in a microclimate-controlled stage top incubator (Tokai Hit, Japan) at 37° C in 5% CO2. Bead displacements and corresponding traction forces fields were calculated using an iterative particle image velocimetry (PIV) algorithm and an unconstrained Fourier transform traction cytometry algorithm, respectively (ImageJ plugins)(Tseng et al., 2012 (link)).
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