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810606P

Avanti

16:0 Tempo PC

Avanti Research - A Croda Brand 810606P, powder

同義詞:

1,2-dipalmitoyl-sn-glycero-3-phospho(tempo)choline

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About This Item

經驗公式(希爾表示法):
C48H94N2O9P
CAS號碼:
分子量::
874.24
MDL號碼:
分類程式碼代碼:
41141825
NACRES:
NA.25
暫時無法取得訂價和供貨情況

化驗

>99% (TLC)

形狀

powder

包裝

pkg of 1 × 1 mg (810606P-1mg)

製造商/商標名

Avanti Research - A Croda Brand 810606P

脂質類型

phospholipids
ESR probes

運輸包裝

dry ice

儲存溫度

−20°C

一般說明

1,2-dipalmitoyl-sn-glycero-3-phospho(tempo)choline (16:0 Tempo PC) is a spin label[1] phospholipid, where TEMPO moiety is attached to phosphocholine headgroup.[2][3]

應用

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]

生化/生理作用

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]

包裝

5 mL Clear Glass Sealed Ampule (810606P-1mg)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

No data available

閃點(°C)

No data available


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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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