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Merck

P3644

Sigma-Aldrich

L-α-Phosphatidylcholin

from soybean, Type IV-S, ≥30% (enzymatic)

Synonym(e):

1,2-Diacyl-sn-glycero-3-phosphocholin, 3-sn-Phosphatidylcholin, L-α-Lecithin, Azolectin, PC

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About This Item

CAS-Nummer:
Beilstein:
5209585
EG-Nummer:
UNSPSC-Code:
51321705
NACRES:
NA.25

Biologische Quelle

soybean

Qualitätsniveau

Typ

Type IV-S

Form

solid

Konzentration

≥30% (enzymatic)

Löslichkeit

chloroform: soluble 100 mg/mL, clear to slightly hazy, yellow to orange

Funktionelle Gruppe

phospholipid

Lipid-Typ

phosphoglycerides

Versandbedingung

ambient

Lagertemp.

−20°C

InChI

1S/C42H80NO8P/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-42(45)51-40(39-50-52(46,47)49-37-36-43(3,4)5)38-48-41(44)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2/h14,16,20-21,40H,6-13,15,17-19,22-39H2,1-5H3/b16-14-,21-20-/t40-/m1/s1

InChIKey

JLPULHDHAOZNQI-ZTIMHPMXSA-N

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Anwendung

L-α-Phosphatidylcholine is suitable for use:
  • as a component of human erythroid massive amplification culture (HEMAdef) medium for clinical expansion of human erythroblasts
  • in the chloride efflux assay to examine the chloride permeability of lipid vesicles conferred by soluble CLIC1
  • in an assay to measure solubilized wax synthase activity
  • as a component of buffer A used for the resuspension of the cholate-solubilized catalytic unit of adenylate cyclase
  • as a cryoprotectant for freezing ruminant sperm
  • as a substrate for the estimation of phospholipase activity
  • to make liposomes to assess their efficiency of recruitment of ARF (ADP ribosylation factor) and AP-1 (adaptor protein)
  • in the preparation of the isolated catalytic unit of soluble adenylate cyclase

Biochem./physiol. Wirkung

Phosphatidylcholine is the major membrane phospholipid in eukaryotic cells, forming the structural component of these membranes. It also serves as a reservoir for several lipid messengers and a source for several bioactive lipids such as, lysophosphatidylcholine, phosphatidic acid, diacylglycerol, lysophosphatidylcholine, platelet activating factor, and arachidonic acid.
Ein großes strukturelles Phospholipid im Gehirn, das schätzungsweise 15 % der Gesamtlipide enthält; befindet sich hauptsächlich in der grauen Substanz.

Angaben zur Herstellung

Purified from P 5638

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


Analysenzertifikate (COA)

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W Jiang et al.
Proceedings of the National Academy of Sciences of the United States of America, 98(9), 4966-4971 (2001-04-26)
The stoichiometry of c subunits in the H(+)-transporting F(o) rotary motor of ATP synthase is uncertain, the most recent suggestions varying from 10 to 14. The stoichiometry will determine the number of H(+) transported per ATP synthesized and will directly
Carlos Andres Morales Letona et al.
Polymers, 11(2) (2019-04-10)
Here, we report a facile and effective one-pot approach to prepare uniform amylose-based polymeric microparticles (PMPs) through enzymatic synthesis of short-chain amylose (SCA) followed by spontaneous self-assembly of the SCA in the presence of lecithin. The effect of lecithin on
J W Winslow et al.
The Journal of biological chemistry, 261(17), 7626-7634 (1986-06-15)
ATP analogues were used to study the active site specificity of the catalytic unit (C) of solubilized and partially purified bovine brain caudate nucleus adenylate cyclase. Phenylenediamine ATP (PD-ATP), 8-azido ATP (8-N3ATP), chromium(III) 3'-beta-alanylarylazido ATP (CrATPa), and 2',3'-dialdehyde ATP (oATP)
Abouzar Najafi et al.
Animal reproduction science, 177, 35-41 (2016-12-25)
The aim of this study was to evaluate the effects of glycerol, ethylene glycol or DMSO in a soybean lecithin extender for freezing ram semen. In this study, 20 ejaculates were collected from four Ghezel rams and diluted with soybean
Glucanolytic enzyme production by Schizophyllum commune Fr. during mycoparasitism.
Chiu S C and Tzean S S.
Physiological & Molecular Plant Pathology, 46, 83-94 (1995)

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