Xylene cyanol
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| Xylene cyanol | |
|---|---|
| Image:Xylene cyanol.png | |
| Identifiers | |
| CAS number | |
| SMILES | [Na+].CCNc1ccc(cc1C)/C(=C2/C=C\C(=[NH+]\CC) C(=C2)C)c3ccc(OS([O-])=O)cc3OS([O-])=O |
| Properties | |
| Molecular formula | C25H27N2O6S2Na |
| Molar mass | 538.61 g/mol |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references | |
Xylene cyanol can be used as a color marker to monitor the process of agarose gel electrophoresis and polyacrylamide gel electrophoresis; in 1% agarose gels, it typically migrates at about the same rate as a 4000 base pair DNA fragment. Bromophenol blue and orange G can also be used for this purpose.
Xylene cyanol is also known as xylene cyanole, Acid Blue 147, xylene cyanol FF, C.I. 42135, ,and sometimes as xylene cyanole FF.
References
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

