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10 protocols using polytetrafluoroethylene

1

Quantification of Ginsenosides by HPLC

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FOS (purity ≥95%, with ≤5% moisture) and GOS (purity ≥90%, with ≤5% moisture, ≤8.5% anhydrous lactose and ≤1.5% anhydrous glucose) were purchased from Quantum Hi-Tech (China) Biological Co., Ltd. (Jiangmen, Guangdong, China), and fibersol-2 (purity ≥90%, with ≤6% moisture) was obtained from Matsutani Chemical Industry Co., Ltd. (Itami, Hyogo, Japan). Methanol and acetonitrile were provided by Sigma-Aldrich (St. Louis, MO, USA). Acetone and other analytical chemical solvents were obtained from Beijing Chemical Factory (Beijing, China).
The compounds of ginsenosides Rb1, Rd, F2, CK, and the internal standard (IS) saikosaponin A were supplied by the National Institute for the Control of Biological and Pharmaceutical Products (Beijing, China). The hydrophobic polytetrafluoroethylene (0.22 μm) used for organic solution filtration was obtained from Millipore (Millipore, Germany).
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2

Biodistribution and Excretion Analysis in Zebrafish

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PP pellets,
xylene, THF, and RBITC were purchased from Sigma-Aldrich. Ethyl alcohol
(anhydrous, 99.9%) was purchased from Samchun Chemicals (Seoul, Korea).
Polytetrafluoroethylene (PTFE, 0.2 μm pore size, 47 mm, Omnipore
hydrophilic membrane filter) and polyvinylidene fluoride (PVDF, 0.2
μm pore size, 47 mm, Durapore hydrophilic membrane filter) were
purchased from Millipore, USA. To observe the biodistribution and
excretion using ZFEs, pronase (P8811) and tricaine (ethyl 3-aminobenzoate
methanesulfonate salt) were purchased from Sigma-Aldrich. EW was prepared
by dissolving 5 mM NaCl, 0.17 mM KCl, 0.33 mM CaCl2, and
0.33 mM MgSO4 in 1 L of DW according to previous work.40 (link)
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3

Synthesis of Iron-Magnesium Hydroxide Compounds

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Magnesium chloride hexahydrate (MgCl2·6H2O), iron chloride hexahydrate (FeCl3·6H2O), ammonium hydroxide solution, triethanolamine (TEA, C6H15NO3), acetylene black, and polytetrafluoroethylene (PTFE) were purchased from Sigma-Aldrich. Potassium hydroxide (KOH, 99.99%) and ethanol absolute (EtOH) were purchased from Panreac. All chemicals were used as received. Milli-Q water was obtained from Millipore Milli-Q equipment.
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4

Fabrication of Fluorescent Estradiol Sensor

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Anti-17-estradiol antibody and 17β-estradiol were purchased from Abcam (Cambridge, UK). The Alexa fluor 488-conjugated goat anti-rabbit IgG (H + L) cross-adsorbed secondary antibody was purchased from Thermo Fisher Scientific (Massachusetts, USA). Cysteamine hydrochloride (≥99%), bovine serum albumin (BSA, ≥99%), phosphate-buffered saline (PBS, 1X), (3-aminopropyl)triethoxysilane (APTES, 99%), ethanol (EtOH, 99.8%), polytetrafluoroethylene (PTFE, 99%), perfluoro(n-butyltetrahydrofuran) (FC-40, 99%), and 1H,1H,2H,2H-perfluorodecyltriethoxysilane (97%) were purchased from Sigma Aldrich. A soda-lime glass substrate was bought from ISOLAB Laborgeräte GmbH. Ag and Au pellets (99.99%) were bought from iTASCO (Taewon Scientific Co., Ltd, Korea). Aqueous solutions were prepared using ultrapure water (Thermo Scientific Easypure II, Göteborg, Sweden) with a resistivity of 18.2 MΩ cm.
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5

Alginate-Based Biomaterial Synthesis

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Alginic acid sodium salt from brown algae (Alg, medium viscosity), poly(vinyl alcohol) (PVA, Mw = 130,000, 99+% hydrolyzed), gelatin from porcine skin (Type A), poly(3,4-ethylenedioxythio phene):poly(styrene sulfonate) (PEDOT:PSS, 1.3 wt% dispersion in H2O, conductive grade, 1 S/cm), polytetrafluoroethylene (PTFE), calcium chloride dihydrate (CaCl2·2H2O, assay ≥ 99.0%), barium chloride dihydrate (BaCl2·2H2O, assay ≥ 99%), aluminum chloride hexahydrate (AlCl3·6H2O, assay ≈ 99%), iron chloride (FeCl3, assay ≈ 97%), and lithium sulfate (Li2SO4, assay ≥98.5% (titration)) were purchased from Sigma-Aldrich. Calcium sulfate dihydrate (CaSO4·2H2O, assay ≥ 98.0%), lithium bromide anhydrous (LiBr, assay ≥ 99.0%), ammonium sulfate ((NH4)2SO4, assay ≥ 99.0%), and ethylenediaminetetraacetic acid (EDTA, assay ≥ 99.0%) were purchased from Samchun (South Korea). The glass fiber membrane was purchased from Whatman, Cytiva (USA). The activated carbon (surface area = 1900–2200 m2/g) was purchased from Power Carbon Technology (South Korea). The materials were used as received without further purification. Dulbecco’s modified Eagle medium (DMEM) with high glucose and sodium pyruvate was purchased from Gibco. Fetal bovine serum (FBS), penicillin/streptomycin, and cell counting kit-8 (CCK-8) were purchased from Merck (Germany), Lonza (Switzerland), and Dojindo (Japan), respectively.
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6

Synthesis and Activation of Cu-Ferrite Composite

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Copper (II) chloride (CuCl2.2H2O, 99%, CAS number 10125-13-0, Alfa Aesar, Haverhill, MA, USA) and iron (II) chloride (FeCl2.4H2O, 98%, CAS number 13478-10-9, Alfa Aesar, Haverhill, MA, USA) were used for the synthesis of Cu-ferrite. Ethanol (200 Proof, CAS number 64-17-5) was purchased from Pharmco Aaper Products, Brookfield, CT, USA. Pluronic P123 surfactant (CAS number 9003-11-6) and propylene oxide (CH3CHCH2O, 99%, CAS number 75-56-9) were purchased from Sigma Aldrich, St. Louis, MO, USA. Idaho National Laboratory (INL) supplied the preprocessed corn stover feedstock (avg. size of 1.12 mm). For the activation of hydrochar, analytical-grade KOH (90%, CAS number 1310-58-3, Sigma Aldrich, St. Louis, MO, USA) and hydrochloric acid (HCl, 35.5%, CAS number 7647-01-0, Fisher-Scientific, Hampton, NH, USA) were used. Polytetrafluoroethylene (PTFE 60 wt.% dispersion in water, CAS number 9002-84-0, Sigma Aldrich, St. Louis, MO, USA), Super P conductive carbon black (CAS number 1333-86-4, MSE Supplies, Tucson, AZ, USA), and nickel foam substrates (1.6 mm thick, 99.9% purity, MTI Corporation, Richmond, CA, USA) were utilized for the preparation of working electrodes.
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7

Fabrication and Characterization of Hybrid Supercapacitor Electrodes

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Indium tin oxide glasses (ITO, 7 Ω/sq) were obtained from Xin Yan Technology Limited. N, N-dimethylformamide (DMF) were supplied by Merck. AC, mesoporous carbon, polytetrafluoroethylene (PTFE), polyacrylonitrile (PAN, Mw = 150,000), silver wire (Ag, diam. 0.5 mm), 3, 4-ethylenedioxythiophene (EDOT, 97% purity), lithium perchlorate (LiClO4, ≥97% purity) and manganese (II) sulfate monohydrate (MnSO4•H2O) were purchased from Sigma-Aldrich. KCl and sulphuric acid (H2SO4) were acquired from Fisher Scientific. Acetone and ethanol were supplied from HmbG Chemicals and J. Kollin Chemicals, respectively. Deionised water (18.2 MΩ.cm) was used throughout the experiments. All chemicals were directly used as obtained without further purification.
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8

Electrochemical Characterization of Nanoparticle Electrode

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The slurry of electrode material was prepared from 85 wt% of synthesized nanoparticles, 10 wt% of activated carbon (Sigma-Aldrich) and 5 wt% of polytetrafluoroethylene (Sigma-Aldrich) using ethanol. The working electrode was prepared by a thin coating of this slurry onto a nickel foil (1 cm2) and drying at 80 °C for 8 h. All the electrochemical analyses were performed at room temperature taking 2 M KOH as electrolytic solution. The specific capacitance (Csp), energy density (E), and power density (P) values were calculated from the obtained GCD curves using the following relations [22 (link)]: Csp=Id×TdΔV×m E=12Csp(ΔV)2 P=E×3600Td where Id and Td = discharge-current and discharge time, m = loaded mass of electrode, ΔV = potential window.
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9

Carbon-Coated Na2Fe2F7 Electrodes

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The as-synthesized
Na2Fe2F7 materials were carbon-coated
prior to electrochemical testing to form an electronically conductive
carbon nanocomposite. The pristine materials were combined with carbon
black (Super C65, MTI Corporation) in a 7:2 ratio along with three
10 mm and three 5 mm ZrO2 balls in a 50 mL ZrO2 ball mill jar and ball-milled at 300 rpm for 24 h. The resultant
carbon-coated materials were hand-ground for 30 min with 10 wt % polytetrafluoroethylene
(Sigma-Aldrich), rolled into free-standing film electrodes, and punched
into 6 mm disks with a loading density of 10 mg cm–2. All electrochemical testing occurred in Swagelok-type cells against
Na metal (Sigma) with a glass fiber separator (Whatman GF/D) using
200 μL of an in-house-prepared electrolyte (<20 ppm water
content) of 1 M NaPF6 (Strem Chemicals, 99%) in propylene
carbonate (Sigma, 99.7%) with 2 vol % fluoroethylene carbonate (Sigma-Aldrich,
≥99%).
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10

Electrochemical Sensing with Herringbone CNTs

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Herringbone carbon nanotubes (hCNTs) were purchased from TCI Chemicals. Uric acid (≥ 99%, crystalline) and L-ascorbic acid (reagent grade, crystalline), glucose, dopamine hydrochloride, epinephrine, glutaraldehyde (50%), polytetrafluoroethylene (PTFE, 60 wt%) were provided by Sigma-Aldrich. KH 2 PO 4 and K 2 HPO 4 were supplied by Emsure® and Sigma-Aldrich, respectively. H 2 SO 4 (98%) was provided by AnalaR Normapur®. HClO 4 (60%) was purchased from VWR Chemicals. NaOH and 4-aminobenzoic acid were purchased from Merck. Ultrapure water was obtained from a Purelab Ultra Elga equipment with a resistivity of 18 MΩ cm.
Commercial gold thin-film interdigitated array microelectrodes (Au-IDA) were provided by Micrux Technologies. These devices consist of a working, a counter and a pseudoreference electrodes, all of them made of gold. The working electrode consist of two individual arrays of Au interdigitated electrodes. In the present manuscript, Au-IDA was used as the substrate for the hCNTs electrode because of its electrical properties and portability.
All electrochemical measurements were carried out in a BIOLOGIC SP-300 potentiostat.
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