用同位素标记LZF—1 DNA指纹探针进行人的DNA指纹分析

同位素γ－32P－ATP对LZF－1DNA指纹探针作5＇末端标记后，检测成都地区人群中84名随机个体的DNA指纹，获得了清晰易辨的具有高度个体特异性的DNA指纹图谱．谱带平均数为17．667条，平均等位基因频率为0．167，探针的鉴别机率为4．862×10－10．表明LZF－1DNA指纹探针完全达到了法医学检验中鉴别个体的目的．     

利用分子信标和EXO III放大荧光信号快速检测Ag+

设计新型的DNA探针,其主要功能区域包含适配体区域和分子信标互补区域;当无靶标存在时,羧基荧光素（FAM）的荧光被黑洞猝灭基团（BHQ）猝灭,加入靶标后,Ag⁺与适配体区域特异性结合,使得分子信标与其互补区域发生结合,加入EXO Ⅲ后,分子信标被酶解,从而释放Ag⁺/DNA探针复合物用于下一轮反应,同时产生大量的FAM,因此,可以通过荧光的增强来定量检测靶标的含量.评价了该方法的灵敏度和选择性,探究它在实际样品中的表现能力.结果表明,适配体区域与分子信标间隔2个碱基的DNA探针与分子信标结合效果最好,检测的信噪比最大.该方法对Ag⁺的检测最低下限（LOD）为0.1nmol/L,在0.5~200nmol/L范围内,荧光值与靶标浓度成线性关系（R²=0.994）.对实际样品的检测在20~200nmol/L范围内呈线性关系（R²=0.998）,且能很好的从混合样品中区分10nmol/L Ag⁺.该研究建立的快速检测Ag⁺方法具有良好的线性定量能力和操作性能,且灵敏度高、特异性强,可满足现实的需求.     

电流探头分析设计

分析了电流探头的两大技术指标,传输阻抗及传输阻抗宽频平坦度,并从电流探头物理结构模型出发,构建了电流探头的电路模型,推导出传输阻抗的计算公式,并从电路模型出发,分析了绕线电阻、端接电阻、分布电容对传输阻抗的影响。     

Interfacial forces between silica surfaces measured by atomic force microscopy

Colloidal particle stability and some other interfacial phenomena are governed by interfacial force interactions. The two well known forces are van der Waals force and electrostatic force, as documented by the classical Derjaguin, Landau, Verwey, and Overbeek (DLVO) theory. Moreover, advances in modern instrumentation and colloid science suggested that some short-ranged forces or structure forces are important for relevant colloidal systems. The interfacial and/or molecular forces can be measured as a resultant force as function of separation distance by atomic force microscopy (AFM) colloid probe. This article presents a discussion on AFM colloid probe measurement of silica particle and silica wafer surfaces in solutions with some technical notifications in measurement and data convolution mechanisms. The measured forces are then analyzed and discussed based on the ‘constant charge’ and ‘constant potential’ models of DLVO theory. The di erence between the prediction of DLVO theory and the measured results indicates that there is a strong short-range structure force between the two hydrophilic surfaces, even at extremely low ionic concentration, such as Milli-Q water purity solution.     

石墨探针采样/石墨探针炉原子吸收光谱测定APM中痕量铜

采用一定规格的石墨探针可直接收集大气微料物质（ＡＰＭ）。然后,立即采用石墨探针炉原子吸收光谱测定收集在探针上的ＡＰＭ中痕量铜。方法简便,快速。在０－５５０ｎｇ／ｍＬ范围内,铜的浓度与峰面积吸光度呈良好的线性关系。铜的特征量为２２．０ｐｇ,检出限为６．６ｎｇ／ｍＬ。分析标准参比材料,铜的回收率达９８％,相对标准偏差为３．３％。     

石墨探针收集/石墨探针炉原子吸收法直接测定APM中痕量铅

研究一种直接收集并测定大气微粒物质中痕量有害元素铅的新方法,石墨探针直接收集ＡＰＭ后,用石墨探针炉原子吸收法直接测定收集在探针上的ＡＰＭ中痕量铅。方法特征量为４４．００ｐｇ,检出限为４８．３６ｐｇ,,相对标准偏差为３．２２％,铅学度与峰面积吸光度在０－２５０μｇ／Ｌ范围内呈线性关系,测定标准参比材料,其回收率为９４．４２％＿９９．１４％,并成功地测定了大气微粒物质中痕量铅的含量。     

Design and use of group-specific primers and probes for real-time quantitative PCR

Real-time quantitative polymerase chain reaction (qPCR) has gained popularity as a technique to detect and quantify a specific group of target microorganisms from various environmental samples including soil, water, sediments, and sludge. Although qPCR is a very useful technique for nucleic acid quantification, accurately quantifying the target microbial group strongly depends on the quality of the primer and probe used. Many aspects of conducting qPCR assays have become increasingly routine and automated; however, one of the most important aspects, designing and selecting primer and probe sets, is often a somewhat arcane process. In many cases, failed or non-specific amplification can be attributed to improperly designed primer-probe sets. This paper is intended to provide guidelines and general principles for designing group-specific primers and probes for qPCR assays. We demonstrate the effectiveness of these guidelines by reviewing the use of qPCR to study anaerobic processes and biologic nutrient removal processes. qPCR assays using group-specific primers and probes designed with this method, have been used to successfully quantify 16S ribosomal Ribonucleic Acid (16S rRNA) gene copy numbers from target methanogenic and ammonia-oxidizing bacteria in various laboratory- and full-scale biologic processes. Researchers with a good command of primer and probe design can use qPCR as a valuable tool to study biodiversity and to develop more efficient control strategies for biologic processes.     

基于甘蔗渣衍生碳量子点的荧光适配体探针的制备及其对17β-雌二醇的检测效果

为实现灵敏、快速、特异性地检测水环境中的17β-雌二醇 (E2) ,以甘蔗渣衍生的碳量子点作为荧光信号,核酸适配体 (aptamer) 作为识别元素,构建了一种可以特异性检测E2的荧光探针,通过荧光强度的变化来定量检测E2并对检测效果进行分析。结果表明：核酸适配体能成功修饰在碳量子点的表面形成稳定的荧光探针;200 mg·L⁻¹的碳量子点与1 μmol·L⁻¹的aptamer为荧光探针的最佳构建比例;相对荧光强度与0~10 μg·L⁻¹质量浓度的雌二醇成正比,且最低检测限为0.42 μg·L⁻¹;该荧光探针可成功应用于水体中E2的检测,回收率为93.6%~106.5%。与传统的仪器检测方法相比,该荧光探针检测E2具有良好的选择性和重现性,还具有操作简单、成本低的优点。本研究成果可为核酸适配体构建的荧光探针在水环境检测中的推广应用提供参考。     

寡核苷酸探针LZF－I进行两栖类DNA指纹分析的初步研究

利用寡核苷酸探针ＬＺＦ－Ｉ对两栖类的３属８种２８只个体的冷冻和甲醛固定的肝组织作了检测．所获ＤＮＡ指纹图在个体、种和属间具有特异性．表明该探针进行ＤＮＡ指纹检测可为两栖动物种、属分类提供依据．     

论自然保护区的共同管理

自然保护区是我国可持续发展的重要事业之一,近几年来发展迅猛,取得了丰硕成果.但是,自然保护区的建设和管理还处在初级阶段,存在许多困难和问题.本文分析了自然保护区管理上存在的困难和问题,探讨了如何实施共同管理,旨在为自然保护区建设和管理提供现实依据.