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991.
构建了基于多壁碳纳米管(Multi-walled carbon nanotubes,MWCNTs)和铂纳米颗粒(Pt-nano)的电流型L-乳酸生物传感器。将Sol-gel膜覆盖在L-乳酸氧化酶(L-lactate oxidase,LOD)和MWCNTs/Pt-nano修饰的电极表面。实验结果表明:传感器的最佳工作条件为:检测电压0.5V;缓冲液pH6.4;检测温度25℃。此传感器的响应时间为5s,灵敏度是6.36μA/(mmol/L)。连续检测4星期其活性仍保持90%,线性范围为0.2~2.0mmol/L,且抗干扰能力强。在实际血样的检测中,此传感器与传统的分光光度法具有很好的一致性。 相似文献
992.
Han H Stapels M Ying W Yu Y Tang L Jia W Chen W Zhang Y Qian X 《Analytical and bioanalytical chemistry》2012,404(2):373-388
The CD44 family are type-1 transmembrane glycoproteins which are important in mediating the response of cells to their microenvironment, including regulation of growth, survival, differentiation, and motility. All these important functions have been reported to be regulated by N-glycosylation; however, little is known about this process. In the CD44 family, the most prolific isoform is CD44 standard type (CD44s). In this work, an integrated strategy combining stable isotope labeling, chemical derivatization, hydrophilic-interaction liquid chromatographic (HILIC) separation, and mass spectrometric (MS) identification was used to perform a comprehensive qualitative and quantitative survey of the N-glycosylation of recombinant CD44s. Specifically, the occupation ratios of the N-glycosites were first determined by MS with (18)O labeling; the results revealed five glycosites with different occupation ratios. Next, N-glycans were profiled by chemical derivatization and exoglycosidase digestion, followed by MALDI-TOF-MS and HILIC-ESI-MS-MS analysis. Interestingly, the quantitative analysis showed that non-sialylated, fucosylated complex-type glycans dominated the N-glycans of CD44s. Furthermore, the site-specific N-glycan distributions profiled by LC-ESI-MS(E) indicated that most glycosites bore complex-type glycans, except for glycosite N100, which was occupied by high-mannose-type N-glycans. This is the first comprehensive report of the N-glycosylation of CD44s. Figure Strategies for characterization of the N-glycosylation status of CD44s. 相似文献
993.
Using supported multi-component zinc dicarboxylate catalyst,poly(1,2-propylene carbonate-co-1,2-cyclohexylene carbonate)(PPCHC) was successfully synthesized from carbon dioxide(CO2) with propylene oxide(PO) and cyclohexene oxide(CHO).The conversion of epoxides dramatically increased up to 89.7%(yield:384.2 g of polymer per g of Zn) with increasing reaction temperature from 60℃to 80℃.The optimized reaction temperature is 80℃.The chemical structure,the molecular weight,as well as thermal and mechanical properties of the resulting terpolymers were investigated extensively. When CHO feed content(mol%) is lower than 10%,the PPCHC terpolymers have number average molecular weight(Mn) ranging from 102×103 to 202×103 and molecular weight distribution(MWD) values ranging from 2.8 to 3.5.In contrast to poly(propylene carbonate)(PPC),the introduction of small amount of CHO leads to increase in the glass transition temperature from 38.0℃to 42.6℃.Similarly,the mechanical strength of the synthesized terpolymer is greatly enhanced due to the incorporation of CHO.These improvements in mechanical and thermal properties are of importance for the practical application of PPC. 相似文献
994.
995.
Zhi-Yong HanRui Guo Pu-Sheng WangDian-Feng Chen Han XiaoLiu-Zhu Gong 《Tetrahedron letters》2011,52(45):5963-5967
An asymmetric cyclization of alkynols triggered addition of azlactones catalyzed by a combined catalyst system consisting of a chiral gold phosphate and a phosphoric acid produces conformationally restricted amino acid precursors bearing vicinal quaternary stereogenic centers in high levels of stereoselectivity. 相似文献
996.
997.
硫酸化氧化锆固体超强酸 总被引:1,自引:0,他引:1
硫酸化氧化锆(SZ)是一种固体超强酸催化剂,它能高效催化异构化、烷化、酰化、环化、裂解、酯化和酯交换等多种类型的催化反应。1979年,日本科学家Hino和Arata发现SZ能在室温催化丁烷异构化反应,首次提出了SZ是一种酸性比100%浓硫酸还强一万倍的固体超强酸,从而引起了科学家们对SZ研究的浓厚兴趣。经过了三十多年发展,研究者们在SZ的合成、改性、表征和应用等方面取得了许多新的研究成果。本文综述了SZ几十年来的研究进展,内容主要包括SZ的合成方法,表面结构和酸性机理,研究者们对SZ性质的不同看法,SZ的改性及应用。 相似文献
998.
超临界流体化学热力学 总被引:9,自引:0,他引:9
本文简要介绍了超临界流体的基本概念和性质,评述了化学热力学在超临界萃取、超临界态化学反应、超临界流体制备材料等方面的作用和研究进展,讨论了二氧化碳-离子液体两相体系的热力学行为。 相似文献
999.
1000.
Two new eudesmane sesquiterpene lactones were isolated from the stalk of Lactuca sativa var.anagustata L and their structureswere elucidated by means of spectroscopic methods,including 2D NMR(~1H-~1H COSY,HMBC and NOESY) as 1β-O-β-D-glucopyranosyl-4α-hydroxyl-5α,6β,11βH-eudesma-12,6α-olide(1) and 1β-hydroxyl-15-O-(p-methoxyphenylacetyl)-5α,6β,11βH-eudesma-3-en-12,6α-olide(2). 相似文献