InChI key
ASKSWIKIIFUEOI-UHFFFAOYSA-N
InChI
1S/C17H19N3.ClH/c1-19(2)13-8-9-15-12(10-13)11-14-16(18-15)6-5-7-17(14)20(3)4;/h5-11H,1-4H3;1H
assay
≥98% (HPLC)
form
solid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze, desiccated (hygroscopic), protect from light
color
burnt orange
solubility
DMF: 1 mg/mL, H2O: 1 mg/mL, ethanol: 1 mg/mL
shipped in
ambient
storage temp.
15-25°C
General description
A cell-permeable fluorescent dye that interacts with DNA and RNA by intercalation or electrostatic attractions. When bound to DNA, this cationic dye is spectrally very similar to fluorescein, with an excitation maximum at 502 nm and an emission maximum at 525 nm. Upon association with RNA, the excitation maximum shifts to 460 nm and the emission maximum shifts to 650 nm (red). Often used to measure single- and double-stranded DNA and RNA in the diagnosis, classification, and prognostication of many neoplasms. A very versatile fluorescent stain used in histochemistry and cytochemistry providing information about the in situ content, molecular structure, conformation, and environment of many nucleic acid-containing cell constituents.
A cell-permeable, cationic fluorescent dye that interacts with DNA and RNA by intercalation or electrostatic attractions. When bound to DNA, it is spectrally very similar to fluorescein, with an excitation maximum at 502 nm and an emission maximum at 525 nm. Upon association with RNA, the excitation maximum shifts to 460 nm and the emission maximum shifts to 650 nm (red). Often used to measure single- and double-stranded DNA and RNA in the diagnosis, classification, and prognosis of many neoplasms. A very versatile fluorescent stain used in histochemistry and cytochemistry that can be used to provide information about the in situ content, molecular structure, and conformation of many nucleic acid-containing cell constituents.
Biochem/physiol Actions
Cell permeable: yes
Primary Target
Interacts with DNA and RNA
Interacts with DNA and RNA
Product does not compete with ATP.
Preparation Note
Following reconstitution, store in the refrigerator (4°C). Aqueous stock solutions are stable for up to 1 month at 4°C.
Other Notes
Gonzalez, K., et al. 1995. Curr. Eye Res.14, 269.
Muro-Cacho, C.A., et al. 1995. J. Immunol.154, 5555.
Olivier, R. 1995. Methods Enzymol.251, 270.
Busch, G.L., et al. 1994. Proc. Natl. Acad. Sci. USA91, 9165.
Darzynkiewicz, Z. 1994. Methods Cell. Biol.41, 401.
Delic, J., et al. 1991. Exp. Cell Res.194, 147.
El-Naggar, A.K., et al. 1991. Cytometry12, 330.
Lopez, F., et al. 1991. Cytometry12, 42.
Gurrieri, S., et al. 1990. Biochemistry29, 3396.
Hermansen, D.K., et al. 1989. Cytometry10, 739.
Muro-Cacho, C.A., et al. 1995. J. Immunol.154, 5555.
Olivier, R. 1995. Methods Enzymol.251, 270.
Busch, G.L., et al. 1994. Proc. Natl. Acad. Sci. USA91, 9165.
Darzynkiewicz, Z. 1994. Methods Cell. Biol.41, 401.
Delic, J., et al. 1991. Exp. Cell Res.194, 147.
El-Naggar, A.K., et al. 1991. Cytometry12, 330.
Lopez, F., et al. 1991. Cytometry12, 42.
Gurrieri, S., et al. 1990. Biochemistry29, 3396.
Hermansen, D.K., et al. 1989. Cytometry10, 739.
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Toxicity: Harmful & Carcinogenic / Teratogenic (E)
signalword
Warning
hcodes
Hazard Classifications
Muta. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
监管及禁止进口产品
此项目有
Flow cytometry technique for assessing effects of N-acetylcysteine on apoptosis and cell viability of human immunodeficiency virus-infected lymphocytes.
R Olivier
Methods in enzymology, 251, 270-278 (1995-01-01)
J Delic et al.
Experimental cell research, 194(1), 147-153 (1991-05-01)
The ability of a "vital" dye, acridine orange (AO), to intercalate into the DNA of living cells was investigated by quantitative intensified fluorescence microscopy and digital imaging under various conditions of dye concentration, excitation light intensity, and ionic concentration. Our
S Gurrieri et al.
Biochemistry, 29(13), 3396-3401 (1990-04-03)
The dynamics of individual DNA molecules undergoing orthogonal field alternating gel electrophoresis (OFAGE) have been studied by use of T2 DNA molecules labeled with a dye and visualized with a fluorescence microscope. The mechanism of reorientation used by a molecule
Simultaneous analysis of cellular RNA and DNA content.
Z Darzynkiewicz
Methods in cell biology, 41, 401-420 (1994-01-01)
F Lopez et al.
Cytometry, 12(1), 42-49 (1991-01-01)
The antibody Ki67 is currently used to evaluate the proliferative fraction of solid tumors and some hematological malignancies. We have used phytohemagglutinin (PHA)-stimulated peripheral blood lymphocytes as a model to study the entry of quiescent cells into cell cycle and
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