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CF-MU 荧光参照标准价格 1386
产品规格
产品货号
Ex (nm) | 356 | Em (nm) | 456 |
分子量 | 228.6 | 溶剂 | DMSO |
存储条件 | 在零下15度以下保存, 避免光照 |
产品基本信息
产品名称:CF-MU 荧光参照标准
储存条件:-15℃避光防潮
保质期:24个月
产品物理化学光谱特性
分子量:228.6
化学结构:
溶剂:DMSO
激发波长(nm):356
发射波长(nm):456
产品介绍
CF-MU是美国AAT Bioquest生产的荧光染料,该化合物用作基于CF-MU的酶底物的校准标准。它具有pH依赖性荧光。与伞形酮相比,这种染料具有更低的pKa,使其在生理条件下比伞形酮更具荧光性。金畔生物是AAT Bioquest的中国代理商,为您提供优质的CF-MU。
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溶解方案(溶剂以说明书为准)
0.1 mg | 0.5 mg | 1 mg | 5 mg | 10 mg | |
1 mM | 437.445 µL | 2.187 mL | 4.374 mL | 21.872 mL | 43.745 mL |
5 mM | 87.489 µL | 437.445 µL | 874.891 µL | 4.374 mL | 8.749 mL |
10 mM | 43.745 µL | 218.723 µL | 437.445 µL | 2.187 mL | 4.374 mL |
参考文献
A Novel Fluorogenic Coumarin Substrate for Monitoring Acid Phosphatase Activity at Low pH Environment
Authors: Yang D, Z Li, Y Diwu, H Fu, J Liao, C Wei, and Z Diwu
Journal: Curr Chem Genomics (2008): 48�50
Excited state properties of 7-hydroxy-4-methylcoumarin in the gas phase and in solution. A theoretical study
Authors: Georgieva I, Trendafilova N, Aquino A, Lischka H.
Journal: J Phys Chem A Mol Spectrosc Kinet Environ Gen Theory (2005): 11860
Novel thiocoumarins as inhibitors of TNF-alpha induced ICAM-1 expression on human umbilical vein endothelial cells (HUVECs) and microsomal lipid peroxidation
Authors: Kumar S, Singh BK, Kalra N, Kumar V, Kumar A, Prasad AK, Raj HG, Parmar VS, Ghosh B.
Journal: Bioorg Med Chem (2005): 1605
Measurement of enzyme kinetics using microscale steady-state kinetic analysis
Authors: Gleason NJ, Carbeck JD.
Journal: Langmuir (2004): 6374
Stability of the complexes of some lanthanides with coumarin derivatives. I. Cerium(III)-4-methyl-7-hydroxycoumarin
Authors: Kostova IP, Manolov, II, Radulova MK.
Journal: Acta Pharm (2004): 37
Crystal structure of 7,8-dihydroxy-4-methylcoumarin
Authors: Kurosaki H, Sharma RK, Otsuka M, Goto M.
Journal: Anal Sci (2003): 647
Structural requirements of hydroxylated coumarins for in vitro anti-Helicobacter pylori activity
Authors: Kawase M, Tanaka T, Sohara Y, Tani S, Sakagami H, Hauer H, Chatterjee SS.
Journal: In Vivo (2003): 509
Modifying rates of reductive elimination of leaving groups from indolequinone prodrugs: a key factor in controlling hypoxia-selective drug release
Authors: Everett SA, Swann E, Naylor MA, Stratford MR, Patel KB, Tian N, Newman RG, Vojnovic B, Moody CJ, Wardman P.
Journal: Biochem Pharmacol (2002): 1629
Synthesis and evaluation of novel fluorogenic substrates for the detection of bacterial beta-galactosidase
Authors: Chilvers KF, Perry JD, James AL, Reed RH.
Journal: J Appl Microbiol (2001): 1118
[Effects of 18 alpha-glycyrrhizic acid on rat liver cytochrome P450 isoenzymes and phase II transferase]
Authors: Yang J, Peng RX, Kong R, Yu JP.
Journal: Yao Xue Xue Bao (2001): 321