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Microanalysis Society Awards: 2023 Award Recipients 微量分析学会奖:2023年获奖者
Pub Date : 2023-07-01 DOI: 10.1093/mictod/qaad045
Bradley T De Gregorio, Pat Camus
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引用次数: 0
NetNotes 网络注释
Pub Date : 2023-07-01 DOI: 10.1093/mictod/qaad052
Bob Price, Bev Maleeff
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引用次数: 0
Cover Art 封面
Pub Date : 2023-07-01 DOI: 10.1093/mictod/qaad047
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引用次数: 0
How to Choose the Right AFM Probe for Your Experiment 如何为你的实验选择合适的AFM探针
Pub Date : 2023-07-01 DOI: 10.1093/mictod/qaad055
F Ted Limpoco, David E Beck
Abstract Atomic force microscopes (AFMs) have emerged as the principal enabling tool for nanotechnology research. They are used ubiquitously in a wide range of fields: from 2D materials, semiconductors, ferroelectrics, and batteries to biomolecules, polymers, and cell biology. As the name implies, AFMs are microscopes. However, rather than using focused light or electrons to magnify sample features, AFMs scan a mechanical probe with a very sharp tip over the surface to create a high-resolution 3D topographical image. Further, by modifying the probe composition or structure, other material properties (electrical, mechanical, magnetic, etc.) can be simultaneously measured and mapped onto the topographic image for precise structure/property correlation. Clearly, the probe is key to unlocking the power of the AFM, thus, choosing the right probe is critical. In this article, we will provide novice and experienced users with basic information and guidelines to simplify the AFM probe selection process.
原子力显微镜(AFMs)已经成为纳米技术研究的主要工具。它们被广泛应用于各种领域:从二维材料、半导体、铁电体、电池到生物分子、聚合物和细胞生物学。顾名思义,原子力显微镜就是显微镜。然而,AFMs不是使用聚焦的光或电子来放大样品的特征,而是在表面上扫描带有非常锋利尖端的机械探针,以创建高分辨率的3D地形图像。此外,通过修改探针组成或结构,可以同时测量其他材料特性(电气、机械、磁性等)并将其映射到地形图像上,以实现精确的结构/性能相关性。显然,探针是释放AFM力量的关键,因此,选择合适的探针至关重要。在本文中,我们将为新手和有经验的用户提供基本信息和指南,以简化AFM探针的选择过程。
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引用次数: 0
Dr. Dale Newbury: An Impressive 50-Year Career and Legacy 戴尔·纽伯里博士:令人印象深刻的50年职业生涯和遗产
Pub Date : 2023-07-01 DOI: 10.1093/mictod/qaad051
Cameron Varano Casasanta
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引用次数: 0
Virtual Microscopy – Nature Experience Radical Design (NERD) Jam 虚拟显微镜-自然体验激进设计(NERD) Jam
Pub Date : 2023-07-01 DOI: 10.1093/mictod/qaad054
S. Okerstrom, D. Esponda, Carolina Fernandez-Jansink
This article proposes using microscopy for nature-inspired design in the early stage of “fuzzy front end” radical innovation and sustainable design technology, where it would have a high positive or sustainable impact. To give a taste of what is possible, a live virtual Nature Experience Radical Design (NERD) Jam was created. Instead of starting with a problem, designers, biologists, engineers, microscopists, and curious people were invited to begin with the solution. By observing and empathizing with nature, both in its element and under a microscope, microscopy reveals unique structural adaptations and possible unknown strategies and mechanisms when exploring nature as a series of successful devices in particular environmental contexts. By looking at nature on multiple scales, one can discover unique models to design sustainable solutions for multiple human challenges.
本文建议在“模糊前端”激进创新和可持续设计技术的早期阶段使用显微镜进行自然灵感设计,这将具有很高的积极或可持续影响。为了让大家体验一下什么是可能的,我们创建了一个虚拟的自然体验激进设计(NERD) Jam。设计师、生物学家、工程师、显微镜学家和好奇的人们被邀请从解决方案开始,而不是从问题开始。通过观察和同情自然,无论是在其元素还是在显微镜下,显微镜揭示了独特的结构适应和可能未知的策略和机制,当探索自然作为一系列成功的设备在特定的环境背景下。通过在多个尺度上观察自然,人们可以发现独特的模型,为人类面临的多种挑战设计可持续的解决方案。
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引用次数: 0
Complying with the New NIH Data Management and Sharing Policy 遵守新的NIH数据管理和共享政策
Pub Date : 2023-07-01 DOI: 10.1093/mictod/qaad036
Stacy Winchester
Abstract The National Institutes of Health (NIH) implemented a new Data Management and Sharing Policy on January 25, 2023. This policy replaces the 2003 document and affirms the NIH’s support for open science and data sharing. Almost all proposals for research that will produce scientific data are now required to include a Data Management and Sharing Plan, which lays out how the research team will collect and preserve data to ensure long-term discoverability and access. Researchers must approach their projects with data sharing in mind, to the extent that is ethically, legally, and technically possible.
美国国立卫生研究院(NIH)于2023年1月25日实施了一项新的数据管理和共享政策。该政策取代了2003年的文件,并肯定了NIH对开放科学和数据共享的支持。现在,几乎所有将产生科学数据的研究提案都需要包括数据管理和共享计划,该计划规定了研究团队将如何收集和保存数据,以确保长期的可发现性和访问性。研究人员在处理他们的项目时必须考虑到数据共享,在道德、法律和技术上都是可行的。
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引用次数: 0
Choosing the Best Camera System for Your Biological Light Microscopy Needs: Part I 选择最好的相机系统为您的生物光学显微镜的需要:第一部分
Pub Date : 2023-07-01 DOI: 10.1093/mictod/qaad039
W. G. (. Jerome
Digital imaging has made scientific light microscope imaging much faster and facilitates a range of imaging techniques not previously available. Advances in microscope digital image detection systems over the last decade have played an integral part in establishing digital imaging as the medium of choice for most types of microscopy. Although we still refer to them as cameras, in actuality, current detector systems constitute specific hardware and software components specifically adapted for specific types of microscopy. Although these advances have facilitated data collection with microscopes, the plethora of choices comes with the need to understand which system best suits a specific researcher’s needs. In an effort to help navigate the multiple choices available, this article and a subsequent one will list what I feel are the major parameters to use in the evaluation of different detection systems, describe the major categories of cameras available, and discuss the advantages and pitfalls of each digital image solution.
数字成像使科学光学显微镜成像更快,并促进了一系列以前无法获得的成像技术。在过去十年中,显微镜数字图像检测系统的进步在建立数字成像作为大多数类型显微镜的选择介质方面发挥了不可或缺的作用。尽管我们仍然将它们称为相机,但实际上,当前的检测器系统构成了专门适用于特定类型显微镜的特定硬件和软件组件。尽管这些进步促进了显微镜的数据收集,但随着选择的增多,需要了解哪种系统最适合特定研究人员的需求。为了帮助导航可用的多种选择,本文和后续文章将列出我认为在评估不同检测系统时使用的主要参数,描述可用相机的主要类别,并讨论每种数字图像解决方案的优点和缺点。
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引用次数: 0
Index of Advertisers 广告客户指数
Pub Date : 2023-07-01 DOI: 10.1093/mictod/qaad058
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引用次数: 0
Using Antibodies in Microscopy: A Guide to Immunohistochemistry. Part 3: Post-Embedding Electron Microscopy Techniques 在显微镜下使用抗体:免疫组织化学指南。第3部分:包埋后电子显微镜技术
Pub Date : 2023-07-01 DOI: 10.1093/mictod/qaad050
Christopher J Guerin
Abstract Immunohistochemistry (IHC) is the use of antibodies as probes to determine the localization of proteins in a cell or tissue sample. In microscopy, the technique has been in use since the 1940s by pathologists and research scientists. At first glance it appears a straightforward procedure. In practice, however, an IHC protocol has many steps where problems can occur resulting in either false positive or false negative data. IHC can be used for ultrastructural studies using electron microscopy (EM), but the protocols used for light microscopy must be adapted. While IHC techniques have been published extensively, a certain amount of confusion exists as to how to optimize them. This series of articles describes the steps involved in IHC and their function, and some variations that occur in specific protocols on differing cell and tissue types. It is hoped that a better understanding of these steps will help to guide users in determining the optimal conditions for carrying through IHC protocols.
免疫组织化学(IHC)是使用抗体作为探针来确定细胞或组织样本中蛋白质的定位。在显微镜中,这种技术自20世纪40年代以来一直被病理学家和研究科学家使用。乍一看,这似乎是一个简单的过程。然而,在实践中,IHC方案有许多步骤,在这些步骤中可能出现问题,导致假阳性或假阴性数据。免疫组化可用于电子显微镜(EM)的超微结构研究,但用于光学显微镜的方案必须进行调整。虽然IHC技术已广泛发表,但在如何优化它们方面存在一定数量的混乱。本系列文章描述了免疫组化所涉及的步骤及其功能,以及在不同细胞和组织类型的特定方案中发生的一些变化。希望更好地了解这些步骤将有助于指导用户确定执行IHC方案的最佳条件。
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引用次数: 0
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