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	<title>Nocodazole powder Archives - TheKaneShop</title>
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	<description>Quality research chemicals</description>
	<lastBuildDate>Mon, 29 Apr 2019 03:19:36 +0000</lastBuildDate>
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		<title>Nocodazole</title>
		<link>https://thekaneshop.com/product/nocodazole/</link>
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		<dc:creator><![CDATA[andreas]]></dc:creator>
		<pubDate>Mon, 29 Apr 2019 03:16:34 +0000</pubDate>
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					<description><![CDATA[<p>Nocodazole</p>
<p>CAS NO:31430-18-9</p>
<p>Assay:98%min</p>
<p>Only for research use only</p>
<p>The post <a href="https://thekaneshop.com/product/nocodazole/">Nocodazole</a> appeared first on <a href="https://thekaneshop.com">TheKaneShop</a>.</p>
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										<content:encoded><![CDATA[<p>Nocodazole is an anti‐mitotic drug that has long been used as an experimental tool in cell biology. Although nocodazole is known to bind with high affinity to tubulin and to inhibit microtubule assembly, very little has been done on its precise mechanism of action. In fact, its binding to the different isotypes of tubulin has never been addressed. Although the nocodazole binding site overlaps with that of colchicine, the two drugs are structurally quite different. The tubulin molecule is an α/β heterodimer; both α and β exist as various isotypes whose distribution and drug‐binding properties are significantly different. In this study, we measured the binding affinity of nocodazole for purified tubulin isotypes. Using fluorescence quenching analysis, we found that the binding kinetics of nocodazole with each type of tubulin best fits a two‐affinity Michaelis‐Menten binding model. The apparent dissociation constants for the high‐affinity binding sites are 0.52 ± 0.02 for αβ<sub>II</sub>, 1.54 ± 0.29 for αβ<sub>III</sub>, and 0.29 ± 0.04 for αβ<sub>IV</sub>. Thus, nocodazole has the highest affinity for αβ<sub>IV</sub> and the lowest affinity for αβ<sub>III</sub>. Knowledge of the isotype specificity of nocodazole may allow for development of novel therapeutic agents based on this drug.</p>
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