5-Aminofluorescein (Highly Pure)

<strong>5-Aminofluorescein (Highly Pure)</strong>_x000D_ <strong>Catalog number:</strong> B2012854_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> 347.3 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> 5-AF, Fluoresceinamine isomer 1_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: Aina V, Malavasi G, Magistris C, Cerrato G, Martra G, Viscardi G, Menabue L, Lusvardi G. Conjugation of amino-bioactive glasses with 5-aminofluorescein as probe molecule for the development of pH sensitive stimuli-responsive biomaterials J Mater Sci Mater Med. 2014 Oct;25(10):2243-53._x000D_ 2: Ding R, Frei E, Fardanesh M, Schrenk HH, Kremer P, Haefeli WE. Pharmacokinetics of 5-aminofluorescein-albumin, a novel fluorescence marker of brain tumors during surgery J Clin Pharmacol. 2011 May;51(5):672-8._x000D_ 3: Kremer P, Fardanesh M, Ding R, Pritsch M, Zoubaa S, Frei E. Intraoperative fluorescence staining of malignant brain tumors using 5-aminofluorescein-labeled albumin Neurosurgery. 2009 Mar;64(3 Suppl):ons53-60; discussion ons60-1._x000D_ 4: Ogamo A, Matsuzaki K, Uchiyama H, Nagasawa K. Preparation and properties of fluorescent glycosaminoglycuronans labeled with 5-aminofluorescein Carbohydr Res. 1982 Jul 1;105(1):69-85._x000D_ 5: Kazarian AA, Hilder EF, Breadmore MC. Utilisation of pH stacking in conjunction with a highly absorbing chromophore, 5-aminofluorescein, to improve the sensitivity of capillary electrophoresis for carbohydrate analysis J Chromatogr A. 2008 Jul 18;1200(1):84-91._x000D_ 6: Mchedlov-Petrossyan NO, Cheipesh TA, Roshal AD, Shekhovtsov SV, Moskaeva EG, Omelchenko IV. Aminofluoresceins Versus Fluorescein: Peculiarity of Fluorescence J Phys Chem A. 2019 Oct 17;123(41):8860-8870._x000D_ 7: Senders JT, Muskens IS, Schnoor R, Karhade AV, Cote DJ, Smith TR, Broekman ML. Agents for fluorescence-guided glioma surgery: a systematic review of preclinical and clinical results Acta Neurochir (Wien). 2017 Jan;159(1):151-167._x000D_ 8: Iwata S, Miyauchi S. Biochemical studies on the use of sodium hyaluronate in the anterior eye segment. III. Histological studies on distribution and efflux process of 5-aminofluorescein-labeled hyaluronate Jpn J Ophthalmol. 1985;29(2):187-97._x000D_ 9: Yuan YZ, Ye C, Sun JH, Hu MY, Huo SJ, Zhu YT, Xiang SY, Yu SQ. Toxicokinetics of mono-(2-ethylhexyl) phthalate with low-dose exposure applying fluorescence tracing technique Toxicol Appl Pharmacol. 2022 Jan 1;434:115814._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/31313795">10: Masoomi H, Wang Y, Fang X, Wang P, Chen C, Liu K, Gu H, Xu H. Ultrabright dye-loaded spherical polyelectrolyte brushes and their fundamental structure-fluorescence tuning principles Nanoscale. 2019 Aug 7;11(29):14050-14059. </a>_x000D_ _x000D_ <strong>Products Related to 5-Aminofluorescein (Highly Pure) can be found at</strong> <a href="https://moleculardepot.com/product-category/Chemicals/"> Chemicals</a>