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850358P

Avanti

16:1 (Δ9-Cis) PC

1,2-dipalmitoleoyl-sn-glycero-3-phosphocholine, powder

Sinónimos:

1,2-di-(9Z-hexadecenoyl)-sn-glycero-3-phosphocholine; PC(16:1(9Z)/16:1(9Z))

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About This Item

Fórmula empírica (notación de Hill):
C40H76NO8P
Número de CAS:
4724-96-3
Peso molecular:
730.01
Número MDL:
MFCD00214374
Código UNSPSC:
51191904
NACRES:
NA.25

Ensayo

>99% (TLC)

Formulario

powder

envase

pkg of 2 × 100 mg (850358P-200mg)
pkg of 5 × 100 mg (850358P-500mg)
pkg of 1 × 25 mg (850358P-25mg)

fabricante / nombre comercial

Avanti Research™ - A Croda Brand 850358P

tipo de lípido

phospholipids
cardiolipins

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C

cadena SMILES

[O-]P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(CCCCCCC/C=C\CCCCCC)=O)COC(CCCCCCC/C=C\CCCCCC)=O)=O

Clave InChI

GPWHCUUIQMGELX-VHQDNGOZSA-N

Categorías relacionadas

Descripción general

16:1 (Δ9-Cis) PC (1,2-dipalmitoleoyl-sn-glycero-3-phosphocholine) is a lipid derivative having a phosphocholine backbone. It also has two 16 carbon fatty acid chains each having one cis double bond at 9th carbon.
The list of Phosphatidylcholine products offered by Avanti is designed to provide compounds having a variety of physical properties. Products available include short chain (C3-C8 are water soluble and hygroscopic), saturated, multi-unsaturated and mixed acid PC′s. All of the products are purified by HPLC, and special precautions are taken to protect the products for oxidization and hydrolysis.

Aplicación

16:1 (Δ9-Cis) PC (1,2-dipalmitoleoyl-sn-glycero-3-phosphocholine) may be used to prepare giant unilamellar vesicles (GUVs), to prepare multilamellar vesicles (MLVs), in lipid membrane to study the antibiotic activity of the lantibiotic gallidermin.

Acciones bioquímicas o fisiológicas

Phosphatidylcholine (PC) is known to participate in fusion and transport of membranes.

Envase

5 mL Clear Glass Sealed Ampule (850358P-200mg)
5 mL Clear Glass Sealed Ampule (850358P-25mg)
5 mL Clear Glass Sealed Ampule (850358P-500mg)

Información legal

Avanti Research is a trademark of Avanti Polar Lipids, LLC

también adquirido normalmente con este producto

Referencia del producto
Descripción
Precios

Código de clase de almacenamiento

11 - Combustible Solids

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Certificados de análisis (COA)

Lot/Batch Number

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<BIG><BIG>Pardo JJD, et al</BIG></BIG>
European Biophysics Journal (2017)
Łukasz Syga et al.
Chembiochem : a European journal of chemical biology, 21(9), 1320-1328 (2019-12-10)
Attachment of lipophilic groups is an important post-translational modification of proteins, which involves the coupling of one or more anchors such as fatty acids, isoprenoids, phospholipids, or glycosylphosphatidyl inositols. To study its impact on the membrane partitioning of hydrophobic peptides
Miranda L Schmidt et al.
Biochimica et biophysica acta. Biomembranes, 1862(5), 183196-183196 (2020-01-21)
Lipid bilayers form the basis of cell membranes and the phase behaviour of the membrane has been linked to proper cell function. Model membranes composed of relatively simple mixtures of phospholipids and cholesterol can already exhibit complex phase behaviour. Specifically

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