標(biāo)題: Titlebook: Clinical Proteomics; Methods and Protocol Antonia Vlahou Book 2008 Humana Press 2008 2D electrophoresis.Clinical proteomics.Computational b [打印本頁] 作者: 不正常 時間: 2025-3-21 17:43
書目名稱Clinical Proteomics影響因子(影響力)
書目名稱Clinical Proteomics影響因子(影響力)學(xué)科排名
書目名稱Clinical Proteomics網(wǎng)絡(luò)公開度
書目名稱Clinical Proteomics網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Clinical Proteomics被引頻次
書目名稱Clinical Proteomics被引頻次學(xué)科排名
書目名稱Clinical Proteomics年度引用
書目名稱Clinical Proteomics年度引用學(xué)科排名
書目名稱Clinical Proteomics讀者反饋
書目名稱Clinical Proteomics讀者反饋學(xué)科排名
作者: 少量 時間: 2025-3-21 21:36
Specimen Collection and Handlingrate the desired specimen. The choice of blood specimens, its collection, handling, processing, and storage are important aspects since these characteristics can have a tremendous impact on the results of the analysis..The awareness of clinical practices in medical laboratories and the current knowl作者: 原諒 時間: 2025-3-22 01:47
Tissue Sample Collection for Proteomics Analysisllection for proteomic purposes with emphasis on the most important steps, including timing issues and the procedures for immediate freezing, storage, and microdissection of the cells of interest or “tissue targets” and the lysates for protein isolation for SELDI, MALDI, and 2DGE applications. The p作者: GLOOM 時間: 2025-3-22 07:26
Protein Profiling of Human Plasma Samples by Two-Dimensional Electrophoresisr their corresponding enzyme activities may reflect either a healthy or a diseased state. Given that there is no defined genomic information as to the intact protein components in plasma, protein profiling could be the first step toward its molecular characterization. Several problems exist in the a作者: 貧窮地活 時間: 2025-3-22 10:39 作者: dominant 時間: 2025-3-22 15:43 作者: dominant 時間: 2025-3-22 18:13
MALDI/SELDI Protein Profiling of Serum for the Identification of Cancer Biomarkers combine higher throughput with the ability to observe differential protein expression levels, have been applied to this goal. An example of such a system is the coupling of robotic sample processing to matrix-assisted laser desorption time of flight mass spectrometry (MALDI-TOF-MS). Within this par作者: 數(shù)量 時間: 2025-3-22 23:37
Urine Sample Preparation and Protein Profiling by Two-Dimensional Electrophoresis and Matrix-Assisteso considered one of the most difficult proteomic samples to work with due to its highly variable contents, as well as the presence of various proteins in low abundance or modified forms. In this chapter, we describe simple protocols and troubleshooting tips for urinary protein preparation and profi作者: 富足女人 時間: 2025-3-23 01:45
Combining Laser Capture Microdissection and Proteomics Techniques cells in several DNA and RNA studies, it has been shown that the small number of cells obtained by this technique can also be used for proteomics analysis. Combining laser capture microdissection and different types of mass spectrometers opened ways to find and identify proteins that are specific f作者: 桉樹 時間: 2025-3-23 07:12
Comparison of Protein Expression by Isotope-Coded Affinity Tag Labelingrotein abundance levels. This chapter describes the ICAT labeling procedure in search for the celecoxib-regulated proteins in a colon cancer cell line. Celecoxib, a cyclooxygenase-2 (COX-2) specific inhibitor, is used as a colorectal cancer preventative drug in clinical trials. Here, celecoxib is us作者: persistence 時間: 2025-3-23 10:36 作者: Infect 時間: 2025-3-23 15:11
Label-Free LC-MS Method for the Identification of Biomarkerserential levels of proteins from complex biological samples like plasma or cerebrospinal fluid is one specific approach being used to identify markers of drug action, efficacy, toxicity, etc. Academic investigators are also interested in markers that are diagnostic or prognostic of disease states. W作者: 漂亮 時間: 2025-3-23 21:44
Analysis of the Extracellular Matrix and Secreted Vesicle Proteomes by Mass Spectrometryd by most cell types and is responsible for the three-dimensional structure of the tissue or organ in which they are originated. Many cells also produce or secrete specialized vesicles into the ECM, which are thought to influence the extracellular environment. ECM is not s a physical structure to co作者: parallelism 時間: 2025-3-23 22:53 作者: 吞噬 時間: 2025-3-24 05:14 作者: ellagic-acid 時間: 2025-3-24 09:45 作者: 急性 時間: 2025-3-24 12:22
https://doi.org/10.1007/978-0-387-78608-7llection for proteomic purposes with emphasis on the most important steps, including timing issues and the procedures for immediate freezing, storage, and microdissection of the cells of interest or “tissue targets” and the lysates for protein isolation for SELDI, MALDI, and 2DGE applications. The p作者: 致詞 時間: 2025-3-24 15:58
https://doi.org/10.1007/978-3-031-49532-8r their corresponding enzyme activities may reflect either a healthy or a diseased state. Given that there is no defined genomic information as to the intact protein components in plasma, protein profiling could be the first step toward its molecular characterization. Several problems exist in the a作者: Debark 時間: 2025-3-24 22:16 作者: Asparagus 時間: 2025-3-25 02:04
Safety of Sodium-Cooled Fast Reactors electrophoresis. DIGE combines spectrally resolvable fluorescent dyes (Cy2, Cy3, and Cy5) with sample multiplexing for low technical variation, and uses an internal standard methodology to analyze replicate samples from multiple experimental conditions with unsurpassed statistical confidence for 2D作者: NOCT 時間: 2025-3-25 03:51 作者: TIA742 時間: 2025-3-25 09:35 作者: Ancestor 時間: 2025-3-25 11:40 作者: 流利圓滑 時間: 2025-3-25 19:53
Safety of Thermal Water Reactorsrotein abundance levels. This chapter describes the ICAT labeling procedure in search for the celecoxib-regulated proteins in a colon cancer cell line. Celecoxib, a cyclooxygenase-2 (COX-2) specific inhibitor, is used as a colorectal cancer preventative drug in clinical trials. Here, celecoxib is us作者: elucidate 時間: 2025-3-25 20:55
Defence in Depth of VVER-440 Reactors,of tissue heterogeneity and contamination. We combined the LCM with isotope-coded affinity tag (ICAT) technology and two-dimensional liquid chromatography to investigate the qualitative and quantitative proteomes of hepatocellular carcinoma (HCC). The effects of three different histochemical stains 作者: Fecundity 時間: 2025-3-26 00:57 作者: 膽大 時間: 2025-3-26 07:13 作者: Maximize 時間: 2025-3-26 12:03
Physical Constants and Conversion Factors,protein arrays or suspension microarrays allow simultaneous analysis of a variety of parameters within a single experiment. In suspension microarrays capture antibodies are coupled onto color-coded microspheres..The applications of suspension microarrays are described, which allow to analyze protein作者: etiquette 時間: 2025-3-26 12:43 作者: 多嘴 時間: 2025-3-26 19:18
Clinical Proteomics978-1-59745-117-8Series ISSN 1064-3745 Series E-ISSN 1940-6029 作者: Tartar 時間: 2025-3-27 00:53 作者: 鐵砧 時間: 2025-3-27 02:30
Methods in Molecular Biologyhttp://image.papertrans.cn/c/image/228187.jpg作者: 引導(dǎo) 時間: 2025-3-27 08:41
https://doi.org/10.1007/978-0-387-78608-7correlate tissue morphology with molecular findings. In recent years, the advent of the laser capture microscope, a tool ideally designed for pathologists, has tremendously facilitated the efficiency of collecting tissue targets for molecular analysis.作者: 使長胖 時間: 2025-3-27 09:38
https://doi.org/10.1007/978-1-84996-420-3ration of extracted ion chromatograms. Additionally, we describe methods for transformation and normalization of the quantitative peptide levels in multiplexed measurements to improve precision for statistical analysis. Lastly, we outline how the described methods can be used to design and power biomarker discovery studies.作者: Tailor 時間: 2025-3-27 15:17 作者: Microgram 時間: 2025-3-27 21:33
Label-Free LC-MS Method for the Identification of Biomarkersration of extracted ion chromatograms. Additionally, we describe methods for transformation and normalization of the quantitative peptide levels in multiplexed measurements to improve precision for statistical analysis. Lastly, we outline how the described methods can be used to design and power biomarker discovery studies.作者: 伙伴 時間: 2025-3-28 01:32
Book 2008ge. In .Clinical Proteomics., a select group of?leading researchers has contributed their state-of-the-art methodologies on protein profiling and identification of disease biomarkers in tissues, microdissected cells and body fluids. Experimental approaches involving the application of two-dimensiona作者: Immunoglobulin 時間: 2025-3-28 02:48 作者: 希望 時間: 2025-3-28 09:00 作者: 搏斗 時間: 2025-3-28 14:23
Specimen Collection and Handlingristics can have a tremendous impact on the results of the analysis..The awareness of clinical practices in medical laboratories and the current knowledge allow for identification of specific variables that affect the results of a proteomic study. The knowledge of preanalytical variables is a prerequisite to understand and control their impact.作者: Fresco 時間: 2025-3-28 17:02 作者: analogous 時間: 2025-3-28 19:48
Safety of Thermal Water Reactors protein precipitation, ultrafiltration, and solid phase extraction in combination to the above profiling technologies serve the means for reliable proteomics analysis of one of the most significant yet very complex biological samples.作者: 高度表 時間: 2025-3-29 02:08 作者: 小爭吵 時間: 2025-3-29 03:58
MALDI/SELDI Protein Profiling of Serum for the Identification of Cancer Biomarkersused to generate protein expression profiles reflective of potential peptide changes in serum. This information can be used to identify proteins, which may enable new diagnostic and therapeutic strategies.作者: 無底 時間: 2025-3-29 10:40
Urine Sample Preparation and Protein Profiling by Two-Dimensional Electrophoresis and Matrix-Assiste protein precipitation, ultrafiltration, and solid phase extraction in combination to the above profiling technologies serve the means for reliable proteomics analysis of one of the most significant yet very complex biological samples.作者: ARK 時間: 2025-3-29 14:12
Miniaturized Parallelized Sandwich Immunoassays. The chapter is divided into the generation of suspension microarrays, sample preparation, processing of suspension microarrays, validation of analytical performance, and finally pattern generation using bioinformatics tools.作者: Mammal 時間: 2025-3-29 16:48 作者: 晚來的提名 時間: 2025-3-29 22:44 作者: Mendicant 時間: 2025-3-30 01:00 作者: cataract 時間: 2025-3-30 07:18
Safety of Sodium-Cooled Fast Reactorsng on the underlying variation that can describe different disease states. This chapter focuses on the design and implementation of the DIGE methodology employing the use of a pooled-sample internal standard in conjunction with the minimal CyDye chemistry. Notes are also provided for the use of the 作者: Salivary-Gland 時間: 2025-3-30 08:45
E. Skupinski,B. Tolley,J. Vilainormatics enable to analyze the proteome of not more than 100–200 cells. Obviously, validation of result is essential. The present review describes and discusses the various methods developed to target cell populations of interest by laser microdissection, followed by analysis of their proteome.
