Acridine Orange Base

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Acridine Orange Base

Acridine Orange Base | 494-38-2

Catalog Number A19-0003
Category DNA Stains
Molecular Formula C17H19N3
Molecular Weight 265.35
Catalog Number Size Price Quantity
A19-0003 -- $--

Product Introduction

Acridine orange is a cell-permeable fluorescent probe that stain nucleic acid. Acridine orange is widely used for cell cycle determination and detection of cellular autophagy.

Chemical Information

Related CAS 65-61-2 (monohydrochloride)
Synonyms 3,6-Acridinediamine, N3,N3,N6,N6-tetramethyl-; N3,N3,N6,N6-tetramethyl-3,6-acridinediamine; Euchrysine; Waxoline Orange A; 3,6-Acridinediamine, N,N,N',N'-tetramethyl-; Acridine, 3,6-bis(dimethylamino)-; 3,6-Bis(dimethylamino)acridine; 3,6-Di(dimethylamino)acridine; Acridine orange free base; Brilliant Acridine Orange E; C.I. 46005B; C.I. Solvent Orange 15; NSC 194350; Solvent Orange 15; Acridine Orange Stain; Acridine Orange
Purity ≥95%
IUPAC Name 3-N,3-N,6-N,6-N-tetramethylacridine-3,6-diamine
Canonical SMILES CN(C)C1=CC2=C(C=C1)C=C3C=CC(=CC3=N2)N(C)C
InChI InChI=1S/C17H19N3/c1-19(2)14-7-5-12-9-13-6-8-15(20(3)4)11-17(13)18-16(12)10-14/h5-11H,1-4H3
InChI Key DPKHZNPWBDQZCN-UHFFFAOYSA-N
Solubility Soluble in DMF, DMSO, Ethanol, PBS (pH 7.2)
Density 1.169±0.06 g/cm3
Appearance Yellow Crystalline Solid
Boiling Point 468.6±25.0°C at 760 mmHg
Melting Point 181-182°C
  • Product Specification
  • Application
Excitation 502 nm (dsDNA), 460 nm (ssDNA and RNA), 475 nm (low pH)
Emission 525 nm (dsDNA), 650 nm (ssDNA and RNA), 590 nm (low pH)
Storage Store at -20°C

Acridine Orange Base, a versatile fluorescent dye with specialized applications in bioscience, is known for its various uses. Here are four key applications of Acridine Orange Base:

Nucleic Acid Staining: Widely employed for staining nucleic acids in biological specimens, Acridine Orange Base stands out for its unique property of intercalating with DNA and RNA. Emitting green fluorescence for DNA and red fluorescence for RNA when visualized under a fluorescence microscope, this dye serves as a crucial tool for distinguishing between different nucleic acid types in cells and tissues.

Cell Cycle Analysis: In the realm of flow cytometry, Acridine Orange Base plays a pivotal role in evaluating cell cycle phases by staining cellular DNA. When combined with other markers that highlight specific cell cycle stages, it aids in the precise identification of phases such as G1, S, and G2/M. Such precise analysis is vital for gaining insights into cell proliferation dynamics and understanding how pharmacological agents influence cell cycle progression.

Apoptosis Detection: Harnessing the capabilities of Acridine Orange Base, researchers can detect apoptotic cells through the staining of condensed chromatin and fragmented DNA. By discerning distinct staining patterns among live, apoptotic, and necrotic cells, scientists can gauge cellular health and evaluate responses to therapeutic interventions. This application holds particular significance in the realms of cancer research and drug development, where understanding cellular responses to treatments is paramount.

Parasitological Studies: In the field of parasitology, Acridine Orange Base emerges as a valuable tool for staining parasites like Plasmodium in blood smears. Its unique ability to highlight intracellular parasites against the backdrop of host cells aids in the accurate diagnosis of malaria and other parasitic infections. This application not only enhances the speed and precision of parasitological diagnostics but also proves especially beneficial in resource-constrained settings where rapid and accurate identification of parasites is crucial.

Literatures

PMIDPublication DateTitleJournal
36126548 2022-10-15 Long-term BPA exposure leads to bone malformation and abnormal expression of MAPK/Wnt/FoxO signaling pathway genes in zebrafish offspring Ecotoxicology and environmental safety
29975445 2018-08-01 Antiapoptotic effects of vitamins C and E against cypermethrin-induced oxidative stress and spermatogonial germ cell apoptosis Journal of biochemical and molecular toxicology
25151148 2014-11-01 Enhanced cellular uptake of a TAT-conjugated peptide inhibitor targeting the polo-box domain of polo-like kinase 1 Amino acids
22992911 2013-01-01 Sperm chromatin structure assay (SCSA®) Methods in molecular biology (Clifton, N.J.)
23038670 2012-11-05 Synthesis and biological studies of pyrazolyl-diamine Pt(II) complexes containing polyaromatic DNA-binding groups Chembiochem : a European journal of chemical biology

Patents

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CN-115172600-A A kind of organic solar cell and preparation method thereof 2022-07-25
CN-115177604-A Application of an astragalus isoflavane in the preparation of drugs for protecting the biological stability of BMSCs 2022-07-13
CN-114958744-A A kind of in vitro stem cell expansion culture method and application 2022-07-12
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