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

proptosis

书目名称Apoptosis and Cancer影响因子(影响力)




书目名称Apoptosis and Cancer影响因子(影响力)学科排名




书目名称Apoptosis and Cancer网络公开度




书目名称Apoptosis and Cancer网络公开度学科排名




书目名称Apoptosis and Cancer被引频次




书目名称Apoptosis and Cancer被引频次学科排名




书目名称Apoptosis and Cancer年度引用




书目名称Apoptosis and Cancer年度引用学科排名




书目名称Apoptosis and Cancer读者反馈




书目名称Apoptosis and Cancer读者反馈学科排名

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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

aggressor

,“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

GRAZE

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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