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产地 | American |
品牌 | AAT Bioquest |
货号 | CS86 |
用途 | Research Grade |
包装规格 | 1 g |
纯度 | 98%% |
CAS编号 | 13558-31-1 |
是否进口 | 是 |
产品名称:罗丹明110*荧光参照标准*
CAS:13558-31-1
规格:1g
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:366.80
外观:红色固体
溶剂:DMSO
激发波长(nm):498
发射波长(nm):520
产品介绍
罗丹明110是美国AAT Bioquest生产的罗丹明类染料 ,该化合物是各种基于R110的酶底物的前体。 它还用作基于R110的酶底物的校准标准。与AMC和AFC酶底物相比,荧光R110底物通常更敏感,比AMC和AFC底物具有更长的吸收和荧光波长。
参考文献
N-DEVD-N'-morpholinecarbonyl-rhodamine 110: novel caspase-3 fluorogenic substrates for cell-based apoptosis assay
Authors: Wang ZQ, Liao J, Diwu Z.
Journal: Bioorg Med Chem Lett (2005): 2335
A transgenic mouse model with a luciferase reporter for studying in vivo transcriptional regulation of the human CYP3A4 gene
Authors: Zhang W, Purchio AF, Chen K, Wu J, Lu L, Coffee R, Contag PR, West DB.
Journal: Drug Metab Dispos (2003): 1054
Fluorogenic substrate [Ala-Pro]2-cresyl violet but not Ala-Pro-rhodamine 110 is cleaved specifically by DPPIV activity: a study in living Jurkat cells and CD26/DPPIV-transfected Jurkat cells
Authors: Boonacker E, Elferink S, Bardai A, Fleischer B, Van Noorden CJ.
Journal: J Histochem Cytochem (2003): 959
Design and synthesis of rhodamine 110 derivative and caspase-3 substrate for enzyme and cell-based fluorescent assay
Authors: Cai SX, Zhang HZ, Guastella J, Drewe J, Yang W, Weber E.
Journal: Bioorg Med Chem Lett (2001): 39
Rhodamine 110-linked amino acids and peptides as substrates to measure caspase activity upon apoptosis induction in intact cells
Authors: Hug H, Los M, Hirt W, Debatin KM.
Journal: Biochemistry (1999): 13906
Intracellular accumulation of rhodamine 110 in single living cells
Authors: Jeannot V, Salmon JM, Deumie M, Viallet P.
Journal: J Histochem Cytochem (1997): 403
Flow cytometric determination of aminopeptidase activities in viable cells using fluorogenic rhodamine 110 substrates
Authors: Ganesh S, Klingel S, Kahle H, Valet G.
Journal: Cytometry (1995): 334
Flow cytometric determination of cysteine and serine proteinase activities in living cells with rhodamine 110 substrates
Authors: Klingel S, Rothe G, Kellermann W, Valet G.
Journal: Methods Cell Biol (1994): 449