Toward 10,000-fold Sample Preconcentration Efficiency for Oligosaccharide Analysis in Capillary Elec

来源 :第2届大连国际色谱学术报告会、第37届国际高效液相色谱及相关技术会议、第18届全国色谱学术报告会 | 被引量 : 0次 | 上传用户:eworld5008
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  Capillary electrophoresis (CE) has been used for oligosaccharide analysis due to the high separation performance, but the concentration sensitivity is limited by the short optical pass length.To overcome the low sensitivity problem, we applied large-volume sample stacking with an electroosmotic flow (EOF) pump (LVSEP)1 to CE, which gave up to a 780-fold sensitivity enhancement without the loss of resolution.For further sensitivity improvement, in this study, LVSEP was combined with field-amplified sample iniection (FASI).
其他文献
Two poloidal arrays and a toroidal array of Mimov coils are developed on the J-TEXT tokamak to measure the magnetic fluctuations and study external MHD activities.By the Mimov coils data,the mode Stnl
A soft X-ray pulse height analysis (PHA) system has been designed and installed on J-TEXT tokamak for the study of electron temperature and impurities.The system contains three Silicon Drift Detectors
The ITER cryostat provides a vacuum environment to avoid excessive thermal loads from being applied to the components that operating at cryogenic temperatures.A global mechanical analysis is required
钨(W)具有较高的熔点、低的氚滞留、低的溅射腐蚀率、以及良好的抗等离子体冲刷能力,是目前最有前景的而向等离子体第一壁材料.但是,纯钨存在低温脆性、高温条件下的再结晶脆化以及中子辐照下的脆化等缺点;同时作为护甲材料的钨与作为热沉材料的铜合金之问存在热膨胀系数和杨氏模量的巨大失配,将导致连接界而的热应力集中和热疲劳失效.研究表明,TiC纳米弥散颗粒的加入可以有效改善钨的低温脆性和提高再结晶温度,同时,
高温等离子体的状态方程作为受控热核聚变的关键物理参量,在多粒子参与的受控聚变反应中,通常是采用关联动力学理论求解,根据。体关联函数推导得到等离子体的状态方程。过程比较复杂,特别是BBKGY方程组的计算是个非常大的工作量。对于这个问题,本文提出了简化的物理模型,即波包近似模型,根据量子统计的思想,运用集团展开,推到得到三阶近似的高温高密等离子体的状态方程。对于高温低密度的等离子体,温度范围大约为10
会议
会议
Immunoreceptor tyrosine-based activation motif (ITAM) is a conserved sequence which occurs in a variety of proteins associated with activation, survival, and differentiation.The phosphorylated tyrosin
Recent advances in mass spectrometry (MS) instruments, sample preparation techniques and data analysis tools make large-scale proteome feasible.However, identification of phosphopeptides is still chal