Rhodamine 110 (Highly Pure)

<strong>Rhodamine 110 (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2013086_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 50 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 366.8 g/mol_x000D_ <strong>Supplied as:</strong> Lyophilized Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20°C_x000D_ <strong>Keywords:</strong> RH110, Rhodamine 560, Rhodamine N_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Jiang SH, Cheng YY, Huo TI, Tsai TH. Pharmacokinetics of Rhodamine 110 and Its Organ Distribution in Rats J Agric Food Chem. 2017 Sep 6;65(35):7797-7804._x000D_ 2: Şen FB, Bener M, Apak R. A Simple Determination of Trinitrotoluene (TNT) Based on Fluorescence Quenching of Rhodamine 110 with FRET Mechanism J Fluoresc. 2021 Jul;31(4):989-997._x000D_ 3: Fan J, Ye Y, Chu G, Zhang Z, Fu Y, Li YM, Shi J. Semisynthesis of Ubiquitin and SUMO-Rhodamine 110-Glycine through Aminolysis of Boc-Protected Thioester Counterparts J Org Chem. 2019 Nov 15;84(22):14861-14867._x000D_ 4: Terentyeva TG, Van Rossom W, Van der Auweraer M, Blank K, Hofkens J. Morpholinecarbonyl-Rhodamine 110 based substrates for the determination of protease activity with accurate kinetic parameters Bioconjug Chem. 2011 Oct 19;22(10):1932-8._x000D_ 5: Gooch J, Abbate V, Daniel B, Frascione N. Solid-phase synthesis of Rhodamine_110 fluorogenic substrates and their application in forensic analysis Analyst. 2016 Apr 21;141(8):2392-5._x000D_ 6: Bhattarai N, Chen M, L Pérez R, Ravula S, M Strongin R, McDonough K, M Warner I. Comparison of Chemotherapeutic Activities of Rhodamine-Based GUMBOS and NanoGUMBOS Molecules. 2020 Jul 17;25(14):3272._x000D_ 7: Queirós C, Vinhas S, Oliveira J, Leite A, Silva AMG, Rangel M. Functionalization of Rhodamine Platforms with 3-Hydroxy-4-pyridinone Chelating Units and Its Fluorescence Behavior towards Fe(III) Molecules. 2022 Feb 26;27(5):1567._x000D_ 8: Rangełowa-Jankowska S, Jankowski D, Grobelna B, Gryczyński I, Gryczyński Z, Bogdanowicz R, Bojarski P. Surface-plasmon-coupled emission of Rhodamine_110 in a silica nanolayer Chemphyschem. 2011 Sep 12;12(13):2449-52._x000D_ 9: Bao X, Lu S, Liow JS, Morse CL, Anderson KB, Zoghbi SS, Innis RB, Pike VW. [¹¹C]Rhodamine-123: synthesis and biodistribution in rodents Nucl Med Biol. 2012 Nov;39(8):1128-36._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/10529236">10: Hug H, Los M, Hirt W, Debatin KM. Rhodamine 110-linked amino acids and peptides as substrates to measure caspase activity upon apoptosis induction in intact cells Biochemistry. 1999 Oct 19;38(42):13906-11. </a>_x000D_ _x000D_ <strong>Products Related to Rhodamine 110 (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Dyes/"> Dyes</a>