Tris Buffered Saline (10x) pH 7.5

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SKU: TBD Categories Buffers, Enzyme Immunoassay

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Product Information

ScyTek Tris Buffered Saline (10x) pH of 7.5 is an optimal formulation of pH stabilizers, salts and detergents designed to effectively remove excess material from the microtiter plate wells without disrupting the ELISA binding reaction. By maintaining the proper buffering environment, unbound components can be washed away without suppressing antigen-antibody binding interactions, thereby reducing nonspecific background and increasing the specific signal. Our Wash buffers do not contain hazardous preservatives such as Azide or Mercury that may interfere with antibody-antigen binding interactions. For your convenience wash buffer is offered in a wide variety of formulations to meet the needs of your specific ELISA application. This product can be customized to meet the specific needs of your assay. Inquire about custom vialing, labeling, kit assembly and drop shipping.

Literary References

1. Bar‐On, Pazit, Leslie Crews, Andrew O. Koob, Hideya Mizuno, Anthony Adame, Brian Spencer, and Eliezer Masliah. “Statins Reduce Neuronal α-Synuclein Aggregation in in Vitro Models of Parkinson’s Disease.” Journal of Neurochemistry 105, no. 5 (2008): 1656–67. https://doi.org/10.1111/j.1471-4159.2008.05254.x.
2. Bar‐On, Pazit, Edward Rockenstein, Anthony Adame, Gilbert Ho, Makoto Hashimoto, and Eliezer Masliah. “Effects of the Cholesterol-Lowering Compound Methyl-β-Cyclodextrin in Models of α-Synucleinopathy.” Journal of Neurochemistry 98, no. 4 (2006): 1032–45. https://doi.org/10.1111/j.1471-4159.2006.04017.x.
3. Liew, Michael, Matthew C. Groll, James E. Thompson, Sara L. Call, Joann E. Moser, Justin D. Hoopes, Karl Voelkerding, Carl Wittwer, and Rex S. Spendlove. “Validating a Custom Multiplex ELISA against Individual Commercial Immunoassays Using Clinical Samples.” BioTechniques 42, no. 3 (March 1, 2007): 327–33. https://doi.org/10.2144/000112332.

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