Sandwich ELISA-based methods use Abs that target the expanded polyglutamine (polyQ) tract to quantify mutant huntingtin (mHTT). Using Meso Scale Discovery (MSD) assay, the mHTT signal detected with MW1 Ab correlated with polyQ length and doubled with a difference of only 7 glutamine residues between equivalent amounts of purified mHTTexon1 proteins. Similar polyQ length-dependent effects on MSD signals were confirmed using endogenous full length mHTT from brains of Huntington's disease (HD) knock-in (KI) mice.
View Article and Find Full Text PDFAn organozincate of composition Et3ZnLi and di-tert-butyl ketone react in toluene to form (after hydrolysis) ethyl-di-tert-butylmethanol. The rate is proportional to approximately [Et3ZnLi](-0.5)[ketone](1) when the initial concentration of Et3ZnLi is greater than that of the ketone but proportional to [Et3ZnLi](1)[ketone](-1) when the initial concentration of ketone is greater than that of Et3ZnLi.
View Article and Find Full Text PDFRelative rates of reactions of MeLi with benzophenones in diethyl ether at 0 degrees C that furnish methyldiarylmethanols were determined using slow addition of a MeLi solution to solutions containing an excess of two benzophenones. The additions exhibit a Hammett rho of 0.94.
View Article and Find Full Text PDFIntroduction: Partially implantable hearing devices have been developed to address some of the user-perceived shortcomings of standard amplification systems. Partially implantable devices are purported to provide improved sound quality as a result of decreased occlusion, decreased feedback, and enhanced clarity resulting from increased high-frequency gain. Such improvements may result in greater user satisfaction.
View Article and Find Full Text PDFToluene solutions of composition Et(3)ZnLi react rapidly with aldehydes and ketones to form addition products. Et(3)ZnNa and Et(3)ZnK solutions react readily with the same substrates although metalation, as well as addition, is significant with substrates having alpha-hydrogens. The Et(3)ZnM solutions react with 2-cyclohexenone to give mainly the 1,4-addition product.
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