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Porcine brain l α phosphatidylcholine

Manufactured by Avanti Polar Lipids
Sourced in United States, Albania

Porcine brain L-α-phosphatidylcholine is a lipid product derived from porcine brain tissue. It is a naturally occurring phospholipid that serves as a key structural component of cell membranes.

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2 protocols using porcine brain l α phosphatidylcholine

1

Lipid and Protein Preparation for Biophysical Studies

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The lipids porcine brain L-α-phosphatidylcholine (PC), porcine brain L-α-phosphatidylserine (PS), porcine brain L-α-phosphatidylethanolamine (PE), porcine brain sphingomyelin (SM), bovine liver L-α-phosphatidylinositol (PI), and cholesterol (ovine wool) were purchased from Avanti Polar Lipids (Alabaster, USA). Bovine myelin basic protein 18.5 kDa was purchased from Merck KGaA (Darmstadt, Germany). Buffer solution of N-(2-hydroxyethyl)piperazine-N’-ethanesulfonic acid (HEPES) and sodium chloride (both from Merck KGaA) was prepared with ultrapure water from a Milli-Q Advantage A10 (Millipore S.A.S., Molsheim Cédex, France) with a conductivity lower than 0.055 µS/cm, and it was adjusted with sodium hydroxide (Fisher Scientific, Leicestershire, UK) to pH 7.4. The chloroform used had HPLC grade and was purchased from Carl Roth GmbH & Co. KG (Karlsruhe, Germany). The fluorescent dye 1,2-Dihexadecanoyl-sn-glycero-3-phosphoethanol-amine-N-(lissamine rhodamine B sulfonyl) (Rh−DHPE) was obtained from Life Technologies GmbH (Darmstadt, Germany) and TopFluor® Cholesterol was obtained from Avanti Polar Lipids (Alabaster, USA). All chemicals were used as received without further purification.
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2

Preparation of Lipid Vesicles for Biological Studies

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The 5:3:2 DOPE/DOPS/DOPC lipid
mixture (ESC, product no. 790304), porcine brain l-α-phosphatidylserine
(PS, product no. 840032), porcine brain l-α-phosphatidylcholine
(PC, product no. 840053), and 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-l-serine (POPS, product no. 840034) were
all purchased from Avanti Polar Lipids (Alabaster, AL). ESC, a 7:3
(w:w) porcine brain PC/PS mixture, and synthetic POPS lipid molecules
were dissolved in chloroform by vortexing and dried under a N2 stream, followed by exposure to vacuum for 1 h. Lipid films
were resuspended in PBS buffer by vortexing to a final lipid concentration
of 30 mM. Small unilamellar vesicles (SUVs) were then generated by
sonicating the resuspended lipids in a bath sonicator (P30H, Elma,
Singen, Germany) at 37 kHz and 50% power for ∼2 h at room temperature
to reach optical transparency.
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