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Polycarbonate track etched membrane filter

Manufactured by Cytiva
Sourced in United States

Polycarbonate track-etched membrane filters are a type of laboratory filtration device. They are designed to separate and isolate particles, cells, or microorganisms from liquid samples. The filters feature uniform pore sizes that are created through a controlled track-etching process, allowing for precise filtration.

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3 protocols using polycarbonate track etched membrane filter

1

Covalent and Non-Covalent Functionalization of CNTs

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CNTs (diameters 10-20 nm, length 5-20 µm) were purchased from Arry Nano (Frechen Königsdorf, Germany). Covalent functionalization or oxidation was achieved by a modified procedure, as previously described. 29 CNTs were dispersed in a 3 : 1 volume ratio mixture of sulphuric acid (H 2 SO 4 , 10 M) and nitric acid (HNO 3 , 10 M) by water bath sonication for 1 h (Transsonic t460 water bath sonicator, 85 Watt, 35 kHz), followed by probe sonication using QSonica sonicator (30 effective minutes with 50% on-50% off cycles, amplitude 100%, 25 watts) on ice. For non-covalent functionalization, the CNTs were dispersed in a 1 mg ml -1 solution of carboxymethyl cellulose (CMC) (Sigma) in a 1 : 2 mass ratio by probe sonication. Aggregates and clusters were removed by centrifugation at 8000g. Excess CMC was washed away using a 0.2 µm pore size polycarbonate track-etched membrane filter (Whatman) (Fig. 1a). For covalent functionalization, the strongly acidic mixture was refluxed at 120 °C for 48 h. The oxidised CNTs (Ox-CNTs) were washed extensively (3 cycle of centrifugation, 11 000g, 30 min) and re-dispersed in water. Amorphous carbon residues were removed by overnight stirring of the Ox-CNTs in 10 mM NaOH 30 and filtration washings with water using a 0.1 µm pore size polycarbonate track-etched membrane filter (Whatman) (Fig. 1b).
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2

Phosphatidylserine Liposome Preparation

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Phosphatidylserine (PtdSer) lipids were purchased from Avanti Polar Lipids (Alabaster, AL). For liposome preparation, chloroform was evaporated under a continuous stream of argon gas and subjected to vacuum desiccation overnight. PtdSer lipids were then resuspended at 1 mg/ml concentration in argon-purged liposome buffer (20 mM HEPES, pH 7.5, 150 mM NaCl, 1 mM MgCl2). Liposomes of 0.4-μm average diameter were formed by using 0.4-μm polycarbonate track-etched membrane filters (Whatman) with an Avanti Mini Extruder as per manufacturer’s instructions (Polar Lipids).
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3

Scanning Electron Microscopy of Cells

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For scanning electron microscopy, cells were fixed in in 2% EM grade glutaraldehyde (Electron Microscopy Sciences, USA) for 90 mins. Post fixation, cells were collected by syringe-passage onto 0.1 μm pore 13 mm polycarbonate track-etched membrane filters (Whatman, USA). Washing and fixation were done through the filter as follows: 5 ml 2.5% glutaraldehyde in PBS allowing rest of 10 mins; 10 ml PBS rest 10 mins; 5 ml 30% v/v, 50% v/v, 70% v/v, 90% v/v ethanol in water 5 mins each; 5 ml 100% ethanol twice for 5 mins each. Samples were then dried with hexamethyldisilazane (HMDS, 5 ml, 5 mins). Filters were removed, air dried, and coated with evaporated carbon at high vacuum (Denton 502 evaporator). Cells were imaged with a Hitachi SU70 FESEM at 20 KeV using combined signals from a conventional Everhart-Thornley detector (adjusted to maximise backscattered electron component) and in-lens secondary electron detector.
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