810606P
Avanti
16:0 Tempo PC
Avanti Research™ - A Croda Brand 810606P, powder
Sinónimos:
1,2-dipalmitoyl-sn-glycero-3-phospho(tempo)choline
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1 MG
MXP 16,687.00
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1 MG
MXP 16,687.00
About This Item
Fórmula empírica (notación de Hill):
C48H94N2O9P
Número de CAS:
Peso molecular:
874.24
Número MDL:
Código UNSPSC:
41141825
NACRES:
NA.25
Productos recomendados
Ensayo
>99% (TLC)
Formulario
powder
envase
pkg of 1 × 1 mg (810606P-1mg)
fabricante / nombre comercial
Avanti Research™ - A Croda Brand 810606P
tipo de lípido
phospholipids
ESR probes
Condiciones de envío
dry ice
temp. de almacenamiento
−20°C
Descripción general
Aplicación
1,2-dipalmitoyl-sn-glycero-3-phospho(tempo)choline (16:0 Tempo PC) may be used:
- as a spin-labeled quencher in liposomes to determine fluorophore depth[4]
- as spin-labeled phospholipid along with 1,2-dimyristoyl(d54)-sn-glycero-3-phosphocholine-1,1,2,2-d4-N,N,N-trimethyl-d9 (DMPC-d67) to label lidocaine for paramagnetic relaxation measurements[5]
- as a spin label to investigate the dependence of the packing and polarity of 1,2-dilauroyl-sn-glycero-3-phosphocholine (DLPC) bilayers with temperature or as quenchers of the Laurdan fluorescence to study the Laurdan position in fluid bilayers[1]
Acciones bioquímicas o fisiológicas
1,2-dipalmitoyl-sn-glycero-3-phospho(tempo)choline (16:0 Tempo PC/Tempo-PCSL) can effectively repress Laurdan fluorescence and can also quench the emission of long wavelength state.[1]
Envase
5 mL Clear Glass Sealed Ampule (810606P-1mg)
Información legal
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
No data available
Punto de inflamabilidad (°C)
No data available
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Certificados de análisis (COA)
Lot/Batch Number
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Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
Cíntia C De Vequi-Suplicy et al.
Journal of fluorescence, 16(3), 431-439 (2006-06-23)
Laurdan (2-dimethylamino-6-lauroylnaphthalene) is a hydrophobic fluorescent probe widely used in lipid systems. This probe was shown to be highly sensitive to lipid phases, and this sensitivity related to the probe microenvironment polarity and viscosity. In the present study, Laurdan was
Alexander Kyrychenko et al.
The Journal of membrane biology, 253(1), 73-77 (2019-09-22)
The characterization of the behavior of lipid-attached spin probes in a bilayer is of fundamental importance for correct interpretation of the results of both EPR and fluorescence studies of protein-membrane interactions. The knowledge of the immersion depth of TEMPO spin
Victor Vasquez-Montes et al.
Biochimica et biophysica acta. Proteins and proteomics, 1867(7-8), 691-700 (2019-04-21)
Bcl-xL is a member of the Bcl-2 family of apoptotic regulators, responsible for inhibiting the permeabilization of the mitochondrial outer membrane, and a promising anti-cancer target. Bcl-xL exists in the following conformations, each believed to play a role in the
Diego E Sastre et al.
The Journal of biological chemistry, 295(7), 2136-2147 (2019-12-05)
PlsX plays a central role in the coordination of fatty acid and phospholipid biosynthesis in Gram-positive bacteria. PlsX is a peripheral membrane acyltransferase that catalyzes the conversion of acyl-ACP to acyl-phosphate, which is in turn utilized by the polytopic membrane
Nicole Weizenmann et al.
Biochimica et biophysica acta, 1818(12), 3010-3018 (2012-07-31)
The membrane location of the local anesthetics (LA) lidocaine, dibucaine, tetracaine, and procaine hydrochloride as well as their influence on phospholipid bilayers were studied by ³¹P and ¹H magic-angle spinning (MAS) NMR spectroscopy. The ³¹P NMR spectra of the LA/lipid
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