Electrospun fabrication was performed as described previously (Cui et al., 2009 (link)). A high-voltage (15 kV) direct current was applied to fabricate the PLLA fibrous membrane. The polymeric solution was fed into the needle tip using a syringe pump at an injection rate of 3.0 mL/h. A grounded aluminum foil was used to collect the fibrous membranes. A 15-cm distance was left between the spray head and the collecting device. The first layer was sprayed with ethylalcohol and vacuum-dried for 1 day before collecting the second layer on the same foil. The second layer was sprayed with ethylalcohol and dried under the same conditions as those used for the first layer.
Polyethylene glycol peg 6000
Polyethylene glycol (PEG) 6000 is a high molecular weight, water-soluble polymer. It is commonly used as a component in various laboratory applications, including gel electrophoresis, protein purification, and cell culture media. PEG 6000 has a molecular weight of approximately 6,000 g/mol and exhibits a range of physicochemical properties that make it suitable for these applications.
Lab products found in correlation
15 protocols using polyethylene glycol peg 6000
Synthesis and Electrospinning of PLLA Fibrous Membranes
Electrospun fabrication was performed as described previously (Cui et al., 2009 (link)). A high-voltage (15 kV) direct current was applied to fabricate the PLLA fibrous membrane. The polymeric solution was fed into the needle tip using a syringe pump at an injection rate of 3.0 mL/h. A grounded aluminum foil was used to collect the fibrous membranes. A 15-cm distance was left between the spray head and the collecting device. The first layer was sprayed with ethylalcohol and vacuum-dried for 1 day before collecting the second layer on the same foil. The second layer was sprayed with ethylalcohol and dried under the same conditions as those used for the first layer.
Protein Purification and Analysis
Garlic Alliin Extraction and Quantification
Maize Lines Drought Tolerance Assay
Characterization of PEGylated ZnO Nanoparticles
Purification of Factor IX Protein
Purification of Moringa Leaf Compounds
Synthesis and Characterization of Iron-Citrate Nanoparticles
Sephacryl s-100 High Resolution was purchased by GE Healthcare Institute (Sweden). The phosphate-buffered saline (PBS) buffer was bought from Sangon Biotech (Shanghai, China) Co., Ltd. The BCA protein content kit was purchased from DingGuo Company (Beijing, China). The TIANamp Bacteria DNA Kit was obtained from Tiangen Bio (Beijing, China). Deionized water and S. aureus were from the School of Public Health, Jilin University.
FMDV Antigen Purification Protocol
Then, viruses were inactivated by the addition of 3 mM binary-ethylenimine (BEI) (Sigma-Aldrich, St. Louis, MO, USA) and incubated in a shaking incubator at 26 °C for 24 h [15 (link)]. Residual BEI was quenched using 2% sodium thiosulfate (Daejung Chemicals, Siheung-si, Korea). The inactivated FMDV culture supernatant was concentrated by mixing it with a final concentration of 7.5% (w/v) polyethylene glycol (PEG) 6000 (Sigma-Aldrich) and 0.5 M NaCl (Sigma-Aldrich). The precipitate was obtained by centrifugation (10,000× g for 30 min) and further purified by sucrose gradient ultracentrifugation as described in a previous study [16 (link)]. The purified 146S antigen was then resuspended in each buffer and excipient composition.
Dapagliflozin Formulation Development
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