Titlebook: Apoptosis and Cancer; Methods and Protocol Gil Mor,Ayesha B. Alvero Book 2015Latest edition Springer Science+Business Media New York 2015 a

proptosis

書目名稱Apoptosis and Cancer影響因子(影響力)




書目名稱Apoptosis and Cancer影響因子(影響力)學(xué)科排名




書目名稱Apoptosis and Cancer網(wǎng)絡(luò)公開度




書目名稱Apoptosis and Cancer網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Apoptosis and Cancer被引頻次




書目名稱Apoptosis and Cancer被引頻次學(xué)科排名




書目名稱Apoptosis and Cancer年度引用




書目名稱Apoptosis and Cancer年度引用學(xué)科排名




書目名稱Apoptosis and Cancer讀者反饋




書目名稱Apoptosis and Cancer讀者反饋學(xué)科排名

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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

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,“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

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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

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,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

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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

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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

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