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Filter paper

Manufactured by Cytiva
Sourced in United Kingdom, United States, Germany, China

Filter paper is a laboratory consumable used to separate solid particles from liquids through a filtration process. It is made of highly absorbent cellulose material that allows the liquid to pass through while retaining the solid matter. Filter papers are available in various grades, pore sizes, and diameters to suit different applications and sample types.

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419 protocols using filter paper

1

Negative Staining of pUL51(1-170) Protein

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Copper grids (300 mesh) coated with formvar and continuous carbon (EM Systems Support) were glow discharged in air for 20 s. Three microlitres of 10–100 μM pUL51(1-170) in 20 mM HEPES pH 7.5 or 20 mM tris pH 8.5 was applied to the grid and allowed to adsorb (30 s to 2 min) before wicking away excess solvent with filter paper (Whatman). Grids were sequentially applied to two 30 µL drops of 2% (w/v) uranyl acetate for approximately 3 s and then 30 s, respectively. Excess stain was wicked away using filter paper (Whatman) and grids were allowed to air dry. Images were obtained using a Tecnai Spirit transmission electron microscope (FEI) operating at 120 kV, equipped with an Ultrascan 1000 CCD camera (Gatan). Images were acquired at 30,000–120,000 × magnification with −1 μm defocus and a total electron dose of 20–40 e/A2 across 1 s exposures.
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2

Negative Staining of Protein Samples

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A sample volume of 3 μL at a concentration of 70 μg/mL protein in 50 mM Tris pH 8, 150 mM NaCl, 5% v/v glycerol was applied to a freshly glow-discharged 300-mesh copper grid (Ted Pella) and incubated on the grid for 1 min. The grid was then dipped in a 40 μL droplet of water, excess liquid was blotted away with filter paper (Whatman), the grid was dipped into 3 μL of 0.75% w/v uranyl formate stain, stain was immediately blotted off with filter paper, then the grid was dipped again into another 3 μL of stain and incubated for ∼30 seconds. Finally, the stain was blotted away and the grids were allowed to dry for 1 minute prior to storage or imaging. Prepared grids were imaged in a Talos model L120C transmission electron microscope using a Gatan camera at 57,000×.
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3

Negative Staining of Protein Samples

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A sample volume of 3 μL at a concentration of 70 μg/mL protein in 50 mM Tris pH 8, 150 mM NaCl, 5% v/v glycerol was applied to a freshly glow-discharged 300-mesh copper grid (Ted Pella) and incubated on the grid for 1 min. The grid was then dipped in a 40 μL droplet of water, excess liquid was blotted away with filter paper (Whatman), the grid was dipped into 3 μL of 0.75% w/v uranyl formate stain, stain was immediately blotted off with filter paper, then the grid was dipped again into another 3 μL of stain and incubated for ~30 s. Finally, the stain was blotted away and the grids were allowed to dry for 1 min prior to storage or imaging. Prepared grids were imaged in a Talos model L120C transmission electron microscope using a Gatan camera at 57,000×.
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4

Fabrication of GRP-Polymer Coated Filters

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Whatman filter paper of diameter 7 cm was used to be coated with GRP-polymer composites by dip-dry method. Whatman filter paper was dipped in 10 mL of GRP-polymer suspension and incubated at RT for solvent evaporation under controlled atmosphere and deposition of GRP-polymer composite on filter paper. Procedure was performed under biosafety hood on sterilized surfaces and germ free environment.
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5

Negative Staining of Protein Samples

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A sample volume of 3 μL at a concentration of 70 μg/mL protein in 50 mM Tris pH 8, 150 mM NaCl, 5% v/v glycerol was applied to a freshly glow-discharged 300-mesh copper grid (Ted Pella) and incubated on the grid for 1 min. The grid was then dipped in a 40 μL droplet of water, excess liquid was blotted away with filter paper (Whatman), the grid was dipped into 3 μL of 0.75% w/v uranyl formate stain, stain was immediately blotted off with filter paper, then the grid was dipped again into another 3 μL of stain and incubated for ~30 s. Finally, the stain was blotted away and the grids were allowed to dry for 1 min prior to storage or imaging. Prepared grids were imaged in a Talos model L120C transmission electron microscope using a Gatan camera at 57,000×.
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6

Trace Metal Analysis of Teff Samples

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Applying the optimized conditions, 0.5 g of powdered each types of teff samples were transferred into a 100 mL round bottom flask. Then 6 mL of a mixture of HNO3 (69-72%) and HClO4 (70%) with a volume ratio of 5:1 (v/v) was added and the mixture was digested on a Kjeldahl digestion apparatus fitted with a reflux condenser by setting the parameters temperature and time. The digest was allowed to cool to room temperature for 10 min without dismantling the condenser and for 10 min after removing the condenser. To the cooled solution 10 mL of distilled water was added to dissolve the precipitate formed on cooling and to minimize dissolution of filter paper by the digest residue while filtering with filter paper (Whatman 125 mm diameter, Germany) into 50 mL volumetric flask. The round bottom flask was rinsed subsequently with around 5 mL distilled water until the total volume reached around 40 mL. Then finally the solution was filled to the mark (50 mL) using distilled water. The digestion was carried out in triplicate for each sample. Digestion of the blank was also performed in parallel with the teff samples keeping all digestion parameters the same. Then the metal concentrations in the digested sample solutions were determined by using MP-AES (Agilent technologies, Inc., 2016).
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7

Serological Surveys for Dengue Infection

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Two serological surveys were undertaken to assess recent dengue infection. The first was conducted nine months after the ITMs were distributed (April 2007) and the second, 32 months after distribution (April 2009). All households with children under the age of 8 were invited to participate. Written informed consent was obtained from the head of household and a blood sample was obtained from one child under 8 years of age in each participating house. The blood sample was collected via finger capillary puncture and was blotted onto an individual piece of filter paper (Whatman). All samples were analysed by dengue IgM capture Enzyme Linked Immunosorbent Assay (ELISA) at Mahidol University’s Centre for Vaccine Development in Bangkok, Thailand.
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8

Damiana Leaf Ethanol Extraction

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A total 100 g Damiana leaves was extracted in 500 mL of 70% ethanol and constantly shaken for 24 h by a Twist shaker at room temperature. The extraction procedure was done thrice. The extracts were collected and subsequently filtered using filter paper (Whatman, Maidstone, Knent, UK). Then, the sample was concentrated by rotary vacuum evaporation (EYELA WORLD–Tokyo Rikakikai Co., LTD., Tokyo, Japan) at 40 °C. The resulted extract yielded 7.38%.
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9

Nanoparticle Imaging via Uranyl Formate Staining

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Nanoparticles diluted to 0.01 mg/mL in 50 mM Tris pH 8, 150 mM NaCl, were adsorbed to glow-discharged home-made carbon-coated copper grids for 30 seconds. The excess liquid was blotted away with filter paper (Whatman 1) and 3 μL of 2% w/v uranyl formate stain were applied to the grids. Finally, the stain was blotted away, and the grids were allowed to air dry for 1 min. Grids were imaged on a 120kV FEI Tecnai G2 Spirit with a Gatan Ultrascan 4000 4k x 4k CCD camera at 67,000 nominal magnification using a defocus ranging between 1.0 and 2.0 μm and a pixel size of 1.6 Å.
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10

Whole Embryo Explant Culturing

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Whole embryo explant cultures were prepared using filter paper extraction (Chapman et al., 2001 (link)). Two adjacent 0.5cm holes are punched on a 2cm × 2cm piece of filter paper (Whatman). Eggs were opened into a petri dish where the embryo will be found near the top of the yolk. The thick albumin is swept aside gently with small filter paper pieces with a tweezer. The holed filter paper is then lowered to attach to the vitelline membrane with the holes allowing embryos to be viewed. The vitelline membrane is then cut around the filter paper to release the embryo. The filter culture embryo is then rinsed in PBS to remove excess yolk. Cleaned embryo is placed on a 3.5cm petri dish containing 2ml of semi-liquid culture media made with the following formula (per 100ml of culture media): Part A: 50ml Albumin (beaten for 15min) then supplement with 0.8ml 20% D-Glucose (Sigma); Part B: 0.3g BactoAgar (Sigma) solved in 50ml water in a microwave then supplement with 1.23ml 5M NaCl. Warm part A and cool part B to 55°C in a water bath. Mix thoroughly and add to petri dishes before gelation. The embryo cultures are maintained in a slide box with wet paper towels in the 37.5°C ~60% humidity egg incubators except when surgeries or snapshot imaging are performed.
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