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Injections were sterilized by 0.22-μm filter membrane.
In Eq. (1), m1 is the dry weight of the blank filter membrane; m2 is the dry weight of loaded filter membrane, V is the volume of sample.
The resulting supernatant was filtered with 0.22-μm filter membrane before the purification process.
Before use, brines were filtered by a 0.45 μm2 filter membrane.
The soluble fractions were resolved by SDS-PAGE and transferred onto nitrocellulose filter membrane.
Sample solutions filtered through a 0.22-μm filter membrane were transferred into the light scattering cells.
After stirring, syringe filter (membrane material: Teflon) was used for filtering.
HepG2 cells can migrate across the pored filter membrane on the transwell [33].
EVs cross the filter membrane and are isolated into a collection solution.
During processing, filters were first dismantled to allow the filter membrane to be extracted.
The MCE filter membrane was peeled off to keep the CuNW network on the PET substrate.
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