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品質等級
化驗
≥97.0% (HPLC)
mp
88 °C (lit.)
溶解度
DMF: soluble
acetonitrile: soluble
methanol: soluble
螢光
λex 366 nm; λem 497 nm in methanol
適合性
suitable for fluorescence
SMILES 字串
CCCCCCCCCCCC(=O)c1ccc2cc(ccc2c1)N(C)C
InChI
1S/C24H35NO/c1-4-5-6-7-8-9-10-11-12-13-24(26)22-15-14-21-19-23(25(2)3)17-16-20(21)18-22/h14-19H,4-13H2,1-3H3
InChI 密鑰
JHDGGIDITFLRJY-UHFFFAOYSA-N
應用
6-十二酰基- N,N -二甲基-2-萘胺 (Laurdan) 是一种用于研究膜结构、顺序和流动性等动态过程的荧光探针。
包裝
无底玻璃瓶。内含物装在插入的融合锥内。
其他說明
荧光膜探针
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
其他客户在看
Simmon Hofstetter et al.
Journal of microbiological methods, 91(1), 93-100 (2012-08-14)
A method for measuring the fluidity of inner membranes of populations of endospores of Clostridium spp. with a fluorescent dye was developed. Cells of Clostridium beijerinckii ATCC 8260 and Clostridium sporogenes ATCC 7955 were allowed to sporulate in the presence
L A Bagatolli et al.
Biochimica et biophysica acta, 1325(1), 80-90 (1997-04-03)
Laurdan (6-dodecanoyl-2-dimethylamine-naphthalene) is a fluorescent membrane probe of recent characterization. It was shown that this probe discriminates between phase transitions, phase fluctuations and the coexistence of phase domains in phospholipid multilamellar aggregates. We measured the excitation and emission generalized polarization
Adéla Melcrová et al.
Scientific reports, 6, 38035-38035 (2016-12-03)
Understanding interactions of calcium with lipid membranes at the molecular level is of great importance in light of their involvement in calcium signaling, association of proteins with cellular membranes, and membrane fusion. We quantify these interactions in detail by employing
L.I. Hellgren
Plant Physiology and Biochemistry, 34, 455-455 (1996)
Luis A Bagatolli et al.
Biomolecules, 9(11) (2019-11-07)
We propose that active metabolic processes may regulate structural changes in biological membranes via the physical state of cell water. This proposition is based on recent results obtained from our group in yeast cells displaying glycolytic oscillations, where we demonstrated
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