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Whatman fusion 5

Manufactured by Cytiva

Whatman Fusion 5 is a laboratory filtration product designed for the efficient separation of particulates from liquid samples. It functions as a high-performance filter membrane with consistent pore size and flow rate, enabling reliable sample preparation for various analytical applications.

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2 protocols using whatman fusion 5

1

Functionalized Filters for Nucleic Acid Capture

Check if the same lab product or an alternative is used in the 5 most similar protocols
Whatman Fusion 5 (Cytiva, Marlborough, MA) was functionalized with chitosan (Sigma-Aldrich, Munich, Germany) using a protocol described by Rosenbohm et al.,33 (link) and stored in a foil zipper lock bag at 4 °C until use. Capture efficiency of functionalized filters was tested using two random short DNA oligos (DNA oligo 1 and DNA oligo 2 in Figure S2d) or yeast tRNA (Sigma-Aldrich, Munich, Germany) by diluting the samples in 1X PBS (pH 5.0–5.4, unless stated otherwise). Functionalized Fusion 5 was inserted into modified Slide-A-Lyzer MINI Dialysis Units (Thermofisher Scientific, Waltham, MA) and the diluted DNA or yeast tRNA was centrifuged through the filter units at 1300 × g or 4000 × g. Differences in the centrifugation speed did not impact capture results. Before and after filtration measurements of the eluate were taken using a NanoDrop Lite Spectrophotometer (Thermofisher Scientific, Waltham, MA). A decrease in nucleic acid concentration in filtered eluate was used to indicated nucleic acid capture (Figure S2 and Table S2).
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2

Functionalized Filters for Nucleic Acid Capture

Check if the same lab product or an alternative is used in the 5 most similar protocols
Whatman Fusion 5 (Cytiva, Marlborough, MA) was functionalized with chitosan (Sigma-Aldrich, Munich, Germany) using a protocol described by Rosenbohm et al.,33 (link) and stored in a foil zipper lock bag at 4 °C until use. Capture efficiency of functionalized filters was tested using two random short DNA oligos (DNA oligo 1 and DNA oligo 2 in Figure S2d) or yeast tRNA (Sigma-Aldrich, Munich, Germany) by diluting the samples in 1X PBS (pH 5.0–5.4, unless stated otherwise). Functionalized Fusion 5 was inserted into modified Slide-A-Lyzer MINI Dialysis Units (Thermofisher Scientific, Waltham, MA) and the diluted DNA or yeast tRNA was centrifuged through the filter units at 1300 × g or 4000 × g. Differences in the centrifugation speed did not impact capture results. Before and after filtration measurements of the eluate were taken using a NanoDrop Lite Spectrophotometer (Thermofisher Scientific, Waltham, MA). A decrease in nucleic acid concentration in filtered eluate was used to indicated nucleic acid capture (Figure S2 and Table S2).
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