Acridine Orange Hydrochloride
<strong>Acridine Orange Hydrochloride </strong>_x000D_ <strong>Catalog number:</strong> B2018935_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 10 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 301.81 g/mol_x000D_ <strong>Supplied as:</strong> Solution_x000D_ <strong>Applications:</strong> a molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20℃_x000D_ <strong>Keywords:</strong> N/A_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Ranjan P, Chakraborty B, Chakraborty T. A systematic computational study of acridine derivatives through conceptual density functional theory Mol Divers. 2023 Jun;27(3):1271-1283._x000D_ 2: Mitra P, Chakraborty PK, Saha P, Ray P, Basu S. Antibacterial efficacy of acridine derivatives conjugated with gold nanoparticles Int J Pharm. 2014 Oct 1;473(1-2):636-43._x000D_ 3: Brunk UT, Neuzil J, Eaton JW. Lysosomal involvement in apoptosis Redox Rep. 2001;6(2):91-7._x000D_ 4: Qin J, Liang Q, Wang G, Hao L, Liu X, Wang X, Hu Z, Fang G, Xue L, Zhao Y, Li R, Lv Q, Wen J, Yang G, Han C, Shi Z. Targeted delivery of nuclear targeting probe for bladder cancer using cyclic pentapeptide c(RGDfK) and acridine orange Clin Transl Oncol. 2023 Feb;25(2):375-383._x000D_ 5: Petrović T, Gligorijević N, Belaj F, Aranđelović S, Mihajlović-Lalić LE, Grgurić-Šipka S, Poljarević J. Drug combination study of novel oxorhenium(V) complexes J Inorg Biochem. 2022 Jun;231:111807._x000D_ 6: Rajagopal RE, Balasubramanian M, Kalyanaraman S. Phenylhydrazine hydrochloride induced dosedependent embryo cytotoxicity in zebrafish Bioinformation. 2019 Apr 15;15(4):255-260._x000D_ 7: Mitra P, Chakraborty PK, Saha P, Ray P, Basu S. Antibacterial efficacy of acridine derivatives conjugated with gold nanoparticles Int J Pharm. 2014 Oct 1;473(1-2):636-43._x000D_ 8: Chaitanya MVSK, Reddy POV, Nikhil K, Kumar A, Shah K, Kumar D. Synthesis and anticancer activity studies of indolylisoxazoline analogues Bioorg Med Chem Lett. 2018 Sep 15;28(17):2842-2845._x000D_ 9: Navolokin N, Lomova M, Bucharskaya A, Godage O, Polukonova N, Shirokov A, Grinev V, Maslyakova G. Antitumor Effects of Microencapsulated Gratiola officinalis Extract on Breast Carcinoma and Human Cervical Cancer Cells In Vitro Materials (Basel). 2023 Feb 9;16(4):1470._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/37888447">10: Cao XZ, Zhang BQ, Wang CF, Yin JN, Haider W, Said G, Wei MY, Lu L. A Terphenyllin Derivative CHNQD-00824 from the Marine Compound Library Induced DNA Damage as a Potential Anticancer Agent Mar Drugs. 2023 Sep 27;21(10):512. </a>_x000D_ _x000D_ <strong>Products Related to Acridine Orange Hydrochloride can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>
Product Specifications
Short Description
Catalog Number: B2018935 (10 mg)
Weight
0.15
Length
2
Width
0.5
Height
0.5
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