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標(biāo)題: Titlebook: Apoptosis and Cancer; Methods and Protocol Gil Mor,Ayesha B. Alvero Book 2015Latest edition Springer Science+Business Media New York 2015 a [打印本頁(yè)]

作者: proptosis    時(shí)間: 2025-3-21 19:42
書(shū)目名稱(chēng)Apoptosis and Cancer影響因子(影響力)




書(shū)目名稱(chēng)Apoptosis and Cancer影響因子(影響力)學(xué)科排名




書(shū)目名稱(chēng)Apoptosis and Cancer網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱(chēng)Apoptosis and Cancer網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱(chēng)Apoptosis and Cancer被引頻次




書(shū)目名稱(chēng)Apoptosis and Cancer被引頻次學(xué)科排名




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書(shū)目名稱(chēng)Apoptosis and Cancer年度引用學(xué)科排名




書(shū)目名稱(chēng)Apoptosis and Cancer讀者反饋




書(shū)目名稱(chēng)Apoptosis and Cancer讀者反饋學(xué)科排名





作者: 無(wú)瑕疵    時(shí)間: 2025-3-21 23:40
Flow Cytometry Enumeration of Apoptotic Cancer Cells by Apoptotic Rate,I), i.e., the percentage of apoptotic cells displaying a specific linage antigen (LAg) within a population of cells that remain unfragmented and retain the expression of the LAg. However, this approach has two major limitations. Firstly, apoptotic cells fragment into apoptotic bodies that later disi
作者: aggressor    時(shí)間: 2025-3-22 03:42
,“Multiplexed Viability, Cytotoxicity, and Caspase Activity Assays”,nly more cost efficient, but also provides more information about a compound or treatment. The ability to combine the activity profiles within the same sample provides a level of normalization not possible with parallel assays. Furthermore, multiplexing caspase activity assays with viability and/or
作者: 把手    時(shí)間: 2025-3-22 04:43
A Multiplexed Method for Kinetic Measurements of Apoptosis and Proliferation Using Live-Content Imasingle, user-defined endpoint. We describe a kinetic multiplex assay incorporating the CellPlayer. NucLight Red reagent to measure proliferation and the CellPlayer. Caspase-3/7 reagent to measure apoptosis using the two-color, live-content imaging platform, IncuCyte. ZOOM. High-definition phase-cont
作者: Working-Memory    時(shí)間: 2025-3-22 10:12

作者: 莊嚴(yán)    時(shí)間: 2025-3-22 14:02
,Detection and Quantification of Apoptosis in Primary Cells Using Taqman? Protein Assay,s are used, the disadvantages of the standard methods can make apoptosis detection difficult due to their slow growth rate and replicative senescence, thereby limiting the available cell number and experiment time span. In this chapter, we describe apoptosis detection and quantification using an inn
作者: conscribe    時(shí)間: 2025-3-22 18:25

作者: Fibroid    時(shí)間: 2025-3-22 22:01
Detection of p53 Protein Transcriptional Activity by Chromatin Immunoprecipitation,ntegrity. An important cellular function that is dependent on p53 transcriptional activity is apoptosis or programmed cell death. Indeed, inhibition of p53 transcriptional activity is often observed in cancers as a result of mutations within its DNA-binding domain. In this chapter, we describe the u
作者: GRAZE    時(shí)間: 2025-3-23 03:26
Homogeneous, Bioluminescent Proteasome Assays,proteins involved in cell-cycle control, apoptosis, and angiogenesis led to the recognition of the proteasome as a therapeutic target for cancer [1–6]. The proteasome is also essential for degrading misfolded and aberrant proteins, and impaired proteasome function has been implicated in neurodegerat
作者: 柱廊    時(shí)間: 2025-3-23 06:37

作者: Adenocarcinoma    時(shí)間: 2025-3-23 13:17
Using the Peggy Simple Western System for Fine Needle Aspirate Analysis,soelectric focusing, “charge”) immunoblotting. The enhanced sensitivity and automation of the Simple Western makes it better suited to cancer diagnostics and research than the traditional Western platform. Because of its smaller sample volume requirements, primary cells, such as those obtained from
作者: 復(fù)習(xí)    時(shí)間: 2025-3-23 17:27

作者: dyspareunia    時(shí)間: 2025-3-23 21:51

作者: NOVA    時(shí)間: 2025-3-23 22:38
Measuring Cardiac Autophagic Flux In Vitro and In Vivo,lysosomes. This process creates energy and biomolecules that are used to maintain homeostasis and to serve as an energy source under conditions of acute stress. Autophagic flux is a measure of efficiency or throughput of the pathway. Here, we describe a method for determining autophagic flux in vitr
作者: grieve    時(shí)間: 2025-3-24 05:33
PET Imaging for Tyrosine Kinase Inhibitor (TKI) Biodistribution in Mice,atment of cancer. Although several tyrosine kinase inhibitors (TKIs), such as erlotinib and gefitinib, have demonstrated clinical efficacy via the inhibition of the epidermal growth factor receptor (EGFR), most TKIs are only effective in a small proportion of patients. Positron emission tomography (
作者: immunity    時(shí)間: 2025-3-24 08:50
https://doi.org/10.1007/978-1-4939-1661-0apoptotic pathway; autophagy; cancer; cancer cell subtypes; cellular biology techniques; cellular process
作者: companion    時(shí)間: 2025-3-24 11:21
978-1-4939-5525-1Springer Science+Business Media New York 2015
作者: Carcinogen    時(shí)間: 2025-3-24 17:42

作者: 紅潤(rùn)    時(shí)間: 2025-3-24 22:54
Elemente der Zweiten Nebengruppeg this process. The best recognized biochemical hallmark of both early and late stages of apoptosis is the activation of cysteine proteases (caspases). Detection of active caspase-3 in cells and tissues is an important method for apoptosis induced by a wide variety of apoptotic signals. Most common
作者: 輕快帶來(lái)危險(xiǎn)    時(shí)間: 2025-3-24 23:09
Elemente der Zweiten NebengruppeI), i.e., the percentage of apoptotic cells displaying a specific linage antigen (LAg) within a population of cells that remain unfragmented and retain the expression of the LAg. However, this approach has two major limitations. Firstly, apoptotic cells fragment into apoptotic bodies that later disi
作者: 疏遠(yuǎn)天際    時(shí)間: 2025-3-25 05:08

作者: 排出    時(shí)間: 2025-3-25 08:08

作者: 成份    時(shí)間: 2025-3-25 13:22

作者: 吸引人的花招    時(shí)間: 2025-3-25 19:50

作者: MUTE    時(shí)間: 2025-3-25 20:27

作者: kyphoplasty    時(shí)間: 2025-3-26 02:15

作者: 健談    時(shí)間: 2025-3-26 05:57

作者: 抗體    時(shí)間: 2025-3-26 11:57

作者: 向外才掩飾    時(shí)間: 2025-3-26 15:07
,Elektrische Leitung und Widerst?nde,soelectric focusing, “charge”) immunoblotting. The enhanced sensitivity and automation of the Simple Western makes it better suited to cancer diagnostics and research than the traditional Western platform. Because of its smaller sample volume requirements, primary cells, such as those obtained from
作者: 統(tǒng)治人類(lèi)    時(shí)間: 2025-3-26 19:07

作者: hardheaded    時(shí)間: 2025-3-26 21:21

作者: 懸掛    時(shí)間: 2025-3-27 01:22
,Elektrische Leitung und Widerst?nde,lysosomes. This process creates energy and biomolecules that are used to maintain homeostasis and to serve as an energy source under conditions of acute stress. Autophagic flux is a measure of efficiency or throughput of the pathway. Here, we describe a method for determining autophagic flux in vitr
作者: 人工制品    時(shí)間: 2025-3-27 06:11
Homogene Halbleiterbauelemente,atment of cancer. Although several tyrosine kinase inhibitors (TKIs), such as erlotinib and gefitinib, have demonstrated clinical efficacy via the inhibition of the epidermal growth factor receptor (EGFR), most TKIs are only effective in a small proportion of patients. Positron emission tomography (
作者: AWL    時(shí)間: 2025-3-27 12:46
Gil Mor,Ayesha B. AlveroIncludes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts.Includes supplementary materia
作者: LINES    時(shí)間: 2025-3-27 16:59
Methods in Molecular Biologyhttp://image.papertrans.cn/a/image/159005.jpg
作者: opprobrious    時(shí)間: 2025-3-27 18:09
Elemente der angewandten Elektronikurthermore, fluorescent proteasome assays require column-purified 20S or 26S proteasome (typically obtained from erythrocytes), or proteasome extracts from whole cells, as their samples. To provide assays more amenable to high-throughput screening, we developed a homogeneous, bioluminescent method t
作者: Traumatic-Grief    時(shí)間: 2025-3-27 23:44

作者: Sarcoma    時(shí)間: 2025-3-28 03:34
,Transformatoren und übertrager, for traditionally hard-to-transfect primary cell types. Lentiviral biosensors are ideal for use with fixed and live cell fluorescent microscopy, and are nondisruptive towards cellular function. GFP- or RFP-protein localization matches well with antibody-based immunostaining and demonstrates altered
作者: RAFF    時(shí)間: 2025-3-28 08:52
,Elektrische Leitung und Widerst?nde,pter outlines materials and methods for the: (1) production of HER-2 targeted nanoparticles; (2) establishment of an orthotopic human ovarian cancer xenograft model; (3) monitoring of tumor growth by bioluminescence imaging; (4) administration of targeted nanoparticles followed by NIR optical imagin
作者: CHASM    時(shí)間: 2025-3-28 14:17

作者: 真實(shí)的人    時(shí)間: 2025-3-28 16:07

作者: 充足    時(shí)間: 2025-3-28 21:26

作者: Metastasis    時(shí)間: 2025-3-29 01:41

作者: Generator    時(shí)間: 2025-3-29 03:15
1064-3745 a stand-alone resource for the execution and analysis of the described protocols and as a reference for the study and detection of apoptosis within and outside the area of cancer research. .978-1-4939-5525-1978-1-4939-1661-0Series ISSN 1064-3745 Series E-ISSN 1940-6029
作者: GRIN    時(shí)間: 2025-3-29 09:18
Caspase-3 Activation Is a Critical Determinant of Genotoxic Stress-Induced Apoptosis,assays for examining caspase-3 activation include immunostaining, immunoblotting for active caspase-3, colorimetric assays using fluorochrome substrates, as well as employing the fluorescein-labeled CaspaTag pan-caspase in situ detection kit.
作者: 越自我    時(shí)間: 2025-3-29 15:09

作者: 珠寶    時(shí)間: 2025-3-29 17:18
Detection of p53 Protein Aggregation in Cancer Cell Lines and Tumor Samples, a crucial factor in carcinogenesis, tumor progression, and the response of cancer cells to apoptotic signals. In this chapter, we provide details on various methods for detecting p53 aggregation in cancer cell lines and tumor samples.
作者: 征稅    時(shí)間: 2025-3-29 20:12

作者: 思想上升    時(shí)間: 2025-3-30 00:55
1064-3745 ation advice from the experts.Includes supplementary materia.In .Apoptosis and Cancer: Methods and Protocols., .Second Edition,. expert researches in the field detail the performance of molecular and cellular biology techniques for studying and detecting the activation of the apoptotic pathway. Chap
作者: Insatiable    時(shí)間: 2025-3-30 05:34

作者: SEEK    時(shí)間: 2025-3-30 11:39

作者: 吹氣    時(shí)間: 2025-3-30 12:28
,“Multiplexed Viability, Cytotoxicity, and Caspase Activity Assays”,e sample provides a level of normalization not possible with parallel assays. Furthermore, multiplexing caspase activity assays with viability and/or cytotoxicity assays can support conclusions regarding cytotoxic mechanism and provide normalization, which may help correct for differences in cell number.
作者: 抒情短詩(shī)    時(shí)間: 2025-3-30 16:33





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