標(biāo)題: Titlebook: Cell Imaging Techniques; Douglas J. Taatjes,Brooke T. Mossman Book 2006 Humana Press 2006 Microarray.cell biology.electron microscopy.gene [打印本頁] 作者: Clinton 時(shí)間: 2025-3-21 19:47
書目名稱Cell Imaging Techniques影響因子(影響力)
作者: CHASE 時(shí)間: 2025-3-22 00:12
Subretinal/Submacular Haemorrhagestudies includes light and confocal microscopy, transmission electron microscopy, and scanning electron microscopy. Techniques outlined include negative staining, cryo-electron microscopy, three-dimentional reconstruction, enzyme cytochemistry, immunocytochemistry, and fluorescence imaging.作者: prediabetes 時(shí)間: 2025-3-22 03:51
https://doi.org/10.1007/978-981-99-8561-6ics applications. However, care must be taken in the acquisition, analysis, and interpretation of AFM indentation data. To help make this powerful technique accessible to a broad range of investigators, detailed procedures are provided for all stages of the AFM experiment from sample preparation through data analysis and visualization.作者: Antigen 時(shí)間: 2025-3-22 05:31 作者: saturated-fat 時(shí)間: 2025-3-22 12:40
Imaging and Probing Cell Mechanical Properties With the Atomic Force Microscope,ics applications. However, care must be taken in the acquisition, analysis, and interpretation of AFM indentation data. To help make this powerful technique accessible to a broad range of investigators, detailed procedures are provided for all stages of the AFM experiment from sample preparation through data analysis and visualization.作者: NATTY 時(shí)間: 2025-3-22 15:39
Ophthalmic Signs in Practice of Medicined analysis on the digitally captured images reveals differences in compositional components as influenced by diet, age, and gender. This method can be expanded to employ a rich variety of histochemical and immunohistochemical staining protocols.作者: NATTY 時(shí)間: 2025-3-22 18:12 作者: Generalize 時(shí)間: 2025-3-22 22:38 作者: 口音在加重 時(shí)間: 2025-3-23 04:11 作者: Affluence 時(shí)間: 2025-3-23 07:24 作者: 媒介 時(shí)間: 2025-3-23 12:29 作者: chemoprevention 時(shí)間: 2025-3-23 17:20 作者: 無政府主義者 時(shí)間: 2025-3-23 19:15
Multifluorescence Labeling Techniques and Confocal Laser Scanning Microscopy on Lung Tissue,to localize signaling events in distinct cell types of the lung and determine their status in the cell cycle (resting or nonresting). Moreover, we are able to determine whether various signaling proteins colocalize in cells and the sites affected by asbestos fibers.作者: 參考書目 時(shí)間: 2025-3-24 00:09
Near-Clinical Applications of Laser Scanning Cytometry,rare events and the correlation of imagery with fluorochromatic measurements. In this chapter, we describe early experiments in the study of cytotoxic drug uptake and resistance in human tumor cells and in the study of sputum cells from asthmatic patients, which harness the specific capabilities of LSC to practical clinical problems.作者: venous-leak 時(shí)間: 2025-3-24 05:06 作者: A精確的 時(shí)間: 2025-3-24 07:01
Quantitative Analysis of Atherosclerotic Lesion Composition in Mice,d analysis on the digitally captured images reveals differences in compositional components as influenced by diet, age, and gender. This method can be expanded to employ a rich variety of histochemical and immunohistochemical staining protocols.作者: SENT 時(shí)間: 2025-3-24 12:07 作者: 是比賽 時(shí)間: 2025-3-24 18:26
Book 2006microarray image scanning, near-field scanning optical microscopy, and reflection contrast microscopy round out this eclectic collection of cutting-edge imaging techniques now available. The authors also discuss preparative methods for particles and cells by transmission electron microscopy.作者: mortuary 時(shí)間: 2025-3-24 20:58
1064-3745 out this eclectic collection of cutting-edge imaging techniques now available. The authors also discuss preparative methods for particles and cells by transmission electron microscopy.978-1-61737-394-7978-1-59259-993-6Series ISSN 1064-3745 Series E-ISSN 1940-6029 作者: Muffle 時(shí)間: 2025-3-24 23:37
https://doi.org/10.1007/978-981-99-7619-5al [Ca.] gradients. This chapter describes the application of wide-field digitized video fluorescence microfluorometry and confocal microscopy to quantitatively image Ca. in cells with high temporal and spatial resolution.作者: 嗎啡 時(shí)間: 2025-3-25 07:11 作者: 忘恩負(fù)義的人 時(shí)間: 2025-3-25 10:37 作者: champaign 時(shí)間: 2025-3-25 13:13
Visualizing Calcium Signaling in Cells by Digitized Wide-Field and Confocal Fluorescent Microscopy,al [Ca.] gradients. This chapter describes the application of wide-field digitized video fluorescence microfluorometry and confocal microscopy to quantitatively image Ca. in cells with high temporal and spatial resolution.作者: Lipohypertrophy 時(shí)間: 2025-3-25 18:16 作者: Radiation 時(shí)間: 2025-3-25 20:46 作者: jet-lag 時(shí)間: 2025-3-26 00:14 作者: labyrinth 時(shí)間: 2025-3-26 05:20
https://doi.org/10.1007/978-981-99-7070-4rescence, it can be separated easily from multiple fluorescent probes. It is already proving useful in imaging collagen with high sensitivity in various tissues, including cirrhotic liver, normal and carious teeth, and surgical repair of tendons.作者: Conflict 時(shí)間: 2025-3-26 11:40
https://doi.org/10.1007/978-981-99-7923-3 data that are accurate with the necessary resolution, sensitivity, and precision. Utilization of this proposed testing approach will help eliminate the subjective nature of assessing the CLSM and allow different machines to be compared. These tests are essential if one is to make intensity measurem作者: 慢慢流出 時(shí)間: 2025-3-26 13:45 作者: geometrician 時(shí)間: 2025-3-26 20:32
https://doi.org/10.1007/978-981-99-8561-6nsmission and fluorescence microscopy. The height of the scanning probe is controlled by atomic force interactions between the specimen surface and the probe tip. The control signal can be used for the production of a topographic (nonoptical) image that can be acquired simultaneously. In this chapte作者: 依法逮捕 時(shí)間: 2025-3-27 00:11 作者: Grating 時(shí)間: 2025-3-27 01:17 作者: 顛簸地移動 時(shí)間: 2025-3-27 09:15 作者: 抵消 時(shí)間: 2025-3-27 09:48
Olympic Games and Global Citiesnes and tips are given on how to record the best images with an electron microscope. Although this chapter is geared to researchers new to the field, experts might find it not only useful as a reference but also valuable because of the number of practical tips included.作者: CANDY 時(shí)間: 2025-3-27 15:23
Second-Harmonic Imaging of Collagen,rescence, it can be separated easily from multiple fluorescent probes. It is already proving useful in imaging collagen with high sensitivity in various tissues, including cirrhotic liver, normal and carious teeth, and surgical repair of tendons.作者: ostensible 時(shí)間: 2025-3-27 21:05
Evaluation of Confocal Microscopy System Performance, data that are accurate with the necessary resolution, sensitivity, and precision. Utilization of this proposed testing approach will help eliminate the subjective nature of assessing the CLSM and allow different machines to be compared. These tests are essential if one is to make intensity measurem作者: 散開 時(shí)間: 2025-3-27 22:27
Laser Scanning Cytometry,yping; (8) visual examination, imaging, or sequential analysis of the cells measured earlier upon their relocation, using different probes; (9) . enzyme kinetics and other time-resolved processes; (10) analysis of tissue section architecture; (11) application for hypocellular samples (needle aspirat作者: 淘氣 時(shí)間: 2025-3-28 05:43 作者: ALOFT 時(shí)間: 2025-3-28 09:37
Porosome,tents expelled during secretion. The discovery of the porosome, its isolation, its structure and dynamics at nanometer resolution and in real time, and its biochemical composition and functional reconstitution into artificial lipid membrane have been determined. The molecular mechanism of secretory 作者: 走調(diào) 時(shí)間: 2025-3-28 12:59
Secretory Vesicle Swelling by Atomic Force Microscopy,aquaporin-1 (AQP1) is also present at the zymogen granule membrane and participates in rapid GTP-induced and G.-mediated vesicular water gating and swelling. Isolated zymogen granules exhibit low basal water permeability. However, exposure of granules to GTP results in a marked potentiation of water作者: 入伍儀式 時(shí)間: 2025-3-28 14:37
Reflection Contrast Microscopy,ron microscopy methods for specimen preparation. Therefore, many familiar techniques for ultrathin specimen preparation can be applied. It is essential that only refractive index differences exist in those areas that are of interest and that the further specimen is as optically homogenic as possible作者: beta-cells 時(shí)間: 2025-3-28 21:58 作者: 精致 時(shí)間: 2025-3-28 22:55 作者: 愛哭 時(shí)間: 2025-3-29 03:16 作者: 替代品 時(shí)間: 2025-3-29 07:18 作者: resuscitation 時(shí)間: 2025-3-29 13:05
https://doi.org/10.1007/978-981-99-7619-5lasm and within organelles are tightly controlled and regulate a diverse array of biological activities, including fertilization, cell division, gene expression, cellular metabolism, protein biosynthesis, secretion, muscle contraction, intercellular communication, and cell death. Measurement of intr作者: 脫離 時(shí)間: 2025-3-29 17:17
https://doi.org/10.1007/978-981-99-7619-5teins expressed in various epithelial and other cell types have been linked to the advent of apoptosis, compensatory proliferation, and adaptation to stress. We describe here the use of immunochemistry and multifluorescence approaches using confocal laser scanning microscopy to define the signaling 作者: connoisseur 時(shí)間: 2025-3-29 20:35 作者: 脾氣暴躁的人 時(shí)間: 2025-3-30 03:57 作者: Adornment 時(shí)間: 2025-3-30 04:10 作者: Crater 時(shí)間: 2025-3-30 11:32
Harshith Sourav Gosula,Amit L. Neheteescence emitted from individual cells is measured at several wavelength ranges, rapidly (up to 5000 cells/min), with high sensitivity and accuracy. The following applications of LSC are reviewed: (1) identification of cells that differ in degree of chromatin condensation (e.g., mitotic or apoptotic 作者: 擋泥板 時(shí)間: 2025-3-30 13:17
https://doi.org/10.1007/978-981-99-8561-6atic measurements on clinical samples allows the development of new and practical assays that could influence diagnosis and treatment in a variety of clinical applications. Laser scanning cytometry (LSC) is a very versatile and adaptable technology that allows for the quantitative analysis of cell s作者: 好忠告人 時(shí)間: 2025-3-30 19:35 作者: CRUDE 時(shí)間: 2025-3-30 21:42
Action Learning and Learning Community,tion of RNA from microdissected tissue followed by quantitative reverse transcriptase-polymerase chain (QRT-PCR) reaction permits the analysis of cell-type or microstructure-specific gene expression changes that occur in response to various stimuli in the environment. In our lab, the combination of 作者: 懸掛 時(shí)間: 2025-3-31 00:57
https://doi.org/10.1007/978-981-99-8561-6py number of specific DNA sequences in nuclei or chromosomes. With recent advancements, this technique has found increased application in a number of research areas, including cytogenetics, prenatal diagnosis, cancer research and diagnosis, nuclear organization, gene loss and/or amplification, and g作者: 準(zhǔn)則 時(shí)間: 2025-3-31 06:22 作者: 鑒賞家 時(shí)間: 2025-3-31 10:06 作者: SOW 時(shí)間: 2025-3-31 13:59 作者: Arctic 時(shí)間: 2025-3-31 19:46 作者: Aromatic 時(shí)間: 2025-3-31 23:56 作者: Heretical 時(shí)間: 2025-4-1 05:08
Action Learning and Learning Community, bright-field microscopy. RCM images have very high contrast, which makes them easily applicable for digital image analysis. Because ultrathin sections are mostly used in this method, RCM also functions by bridging light with electron microscopy: the combination of ultrastructural with histochemical作者: 整潔 時(shí)間: 2025-4-1 09:59
Olympic Games and Global Cities novice researcher new to this field to know how to start tackling a new project. This chapter is designed to serve as a guideline for anyone starting a new project to determine a three-dimensional structure using single-particle techniques. The chapter describes the basic techniques necessary to pr
