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標(biāo)題: Titlebook: Detection of Cell Death Mechanisms; Methods and Protocol Ayesha B. Alvero,Gil G. Mor Book 2021 Springer Science+Business Media, LLC, part o [打印本頁(yè)]

作者: 呻吟    時(shí)間: 2025-3-21 18:11
書目名稱Detection of Cell Death Mechanisms影響因子(影響力)




書目名稱Detection of Cell Death Mechanisms影響因子(影響力)學(xué)科排名




書目名稱Detection of Cell Death Mechanisms網(wǎng)絡(luò)公開度




書目名稱Detection of Cell Death Mechanisms網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Detection of Cell Death Mechanisms被引頻次




書目名稱Detection of Cell Death Mechanisms被引頻次學(xué)科排名




書目名稱Detection of Cell Death Mechanisms年度引用




書目名稱Detection of Cell Death Mechanisms年度引用學(xué)科排名




書目名稱Detection of Cell Death Mechanisms讀者反饋




書目名稱Detection of Cell Death Mechanisms讀者反饋學(xué)科排名





作者: 無(wú)聊點(diǎn)好    時(shí)間: 2025-3-21 21:20

作者: deviate    時(shí)間: 2025-3-22 01:37
Subcellular Fractionation to Demonstrate Activation of Intrinsic Apoptotic Pathway,nslational modifications or loss of organelle membrane integrity lead to the movement of proteins from one compartment to another. This movement of proteins or protein translocation, exerts a significant effect on protein function. This is clearly demonstrated in the context of apoptosis wherein the
作者: Peculate    時(shí)間: 2025-3-22 05:15

作者: 生來(lái)    時(shí)間: 2025-3-22 12:22
Flow Cytometric Analyses of p53-Mediated Cell Cycle Arrest and Apoptosis in Cancer Cells,survival, such as disturbance of cell cycle progression, senescence, autophagy, and programmed cell death. One of the best examples is tumor suppressor p53. p53 functions as a tumor suppressor by inducing cell cycle arrest and apoptosis in response to genotoxic and environmental insults. The choice
作者: mechanism    時(shí)間: 2025-3-22 13:34
A Real-Time, Bioluminescent Apoptosis Assay,en employing traditional apoptosis detection chemistries after exposures with inducers of unknown potential. The assay continuously reports the translocation of phosphatidylserine (PS) from the inner membrane leaflet of a cell to the exofacial surface during apoptosis. This homogenous, no-wash, plat
作者: mechanism    時(shí)間: 2025-3-22 18:45
Detection of Anoikis Using Cell Viability Dye and Quantitation of Caspase Activity,ivation of caspases. Specific interaction between cellular receptors such as integrins and the ECM is important to maintain cellular homeostasis in normal tissues through multiple cascades. This interaction provides not only physical attachment, but more importantly, vital interaction with the actin
作者: 抑制    時(shí)間: 2025-3-23 00:03

作者: cortex    時(shí)間: 2025-3-23 02:45

作者: 山崩    時(shí)間: 2025-3-23 08:38
In Vitro Identification and Isolation of Human Neutrophil Extracellular Traps,tuted of a DNA scaffold with associated antimicrobial proteins, which are released to the extracellular space as an effective mechanism to fight against invading microorganisms. In parallel with this beneficial role to avoid microbial dissemination and wall off infections, accumulating evidence supp
作者: 藕床生厭倦    時(shí)間: 2025-3-23 11:14

作者: 上腭    時(shí)間: 2025-3-23 14:36
Visualization of Necroptotic Cell Death through Transmission Electron Microscopy,rent chapter provides detailed guidelines for imaging morphological changes during programmed cell necrosis using TEM as a single-step methodology. In this protocol, a novel aldehyde dehydrogenase inhibitor is used to induce cell programmed necrosis in ovarian cancer cell lines (A2780 and SKOV3). Th
作者: Hemiplegia    時(shí)間: 2025-3-23 18:34

作者: Arteriography    時(shí)間: 2025-3-24 00:00
A Luminescence Assay to Quantify Cell Viability in Real Time, from hours to several days. Here, we describe a sensitive, nonlytic live-cell assay that allows continuous or ‘real-time’ monitoring of cell viability, growth, and cytotoxicity over an extended period of time. We illustrate the use of the assay for small drug molecule and antibody-dependent cytotox
作者: 古代    時(shí)間: 2025-3-24 06:13

作者: 直覺(jué)沒(méi)有    時(shí)間: 2025-3-24 06:57

作者: 采納    時(shí)間: 2025-3-24 11:51
1064-3745 ation advice from the experts.This volume provides detailed protocols for the performance, analysis, and troubleshooting of?.in vitro.?and?.in vivo.?experiments related to programmed cell death. Chapters compile?conventional techniques such as?western blot and qPCR and state-of-the art transmission
作者: Ptosis    時(shí)間: 2025-3-24 15:52
Book 2021med cell death. Chapters compile?conventional techniques such as?western blot and qPCR and state-of-the art transmission electron microscopy and real-time multiplexed imaging assays. ?Written in the highly successful?.Methods in Molecular Biology.?series format, chapters include introductions to the
作者: ensemble    時(shí)間: 2025-3-24 21:55

作者: transient-pain    時(shí)間: 2025-3-25 01:16
Book 2021ir respective topics, application details for both the expert and non-expert reader, and tips on troubleshooting and avoiding known pitfalls...?Authoritative and accessible,?.Detection of Cell Death Mechanisms: Methods and Protocols?.aims to ensure seamless execution of protocols on specific cell death type..
作者: Condescending    時(shí)間: 2025-3-25 06:57
Befruchtung und Entwicklung des Eies,se transcription factors are CHOP and the spliced variant of XBP-1 (XBP1s). In this chapter, we describe a quantitative PCR method to detect the upregulation of CHOP and XBP1s mRNA during Tunicamycin-induced UPR.
作者: Legion    時(shí)間: 2025-3-25 09:43

作者: 扔掉掐死你    時(shí)間: 2025-3-25 11:48

作者: 祖先    時(shí)間: 2025-3-25 17:16
Geb?rde, Laut und graphisches Zeichens were collected at different timepoints, frozen, stored, and analyzed at the end of experiments using the luminescent LDH-Glo? Assay. High assay sensitivity and low volume sampling enabled drug-induced toxicity profiling in a time- and dose-dependent manner.
作者: 小隔間    時(shí)間: 2025-3-25 23:35

作者: 主動(dòng)脈    時(shí)間: 2025-3-26 03:53

作者: Tremor    時(shí)間: 2025-3-26 06:32

作者: judiciousness    時(shí)間: 2025-3-26 11:03
Gebührenprivileg und Beihilferechtm one system (dependent upon selection of target gene) can be overcome through use of the second system. Strategies for optimizing the knockout process and selection of finished cell lines are also presented.
作者: 脾氣暴躁的人    時(shí)間: 2025-3-26 15:48
Detection of Unfolded Protein Response by Polymerase Chain Reaction,se transcription factors are CHOP and the spliced variant of XBP-1 (XBP1s). In this chapter, we describe a quantitative PCR method to detect the upregulation of CHOP and XBP1s mRNA during Tunicamycin-induced UPR.
作者: 失眠癥    時(shí)間: 2025-3-26 19:00

作者: NATAL    時(shí)間: 2025-3-26 21:01

作者: bioavailability    時(shí)間: 2025-3-27 04:10

作者: flutter    時(shí)間: 2025-3-27 08:08

作者: Cpr951    時(shí)間: 2025-3-27 11:07
In Vitro Identification and Isolation of Human Neutrophil Extracellular Traps,perties and their role in pathophysiological processes is a rapidly evolving and expanding field. Here, we describe a combination of methods to achieve a successful in vitro NET visualization, semiquantification, and isolation.
作者: SHRIK    時(shí)間: 2025-3-27 14:07
Induction and Detection of Necroptotic Cell Death in Mammalian Cell Culture,ive controls, detection of necroptosis mediator proteins via Western Blot analysis, and interpretation of results. This protocol allows reliable and specific detection of necroptosis in cell culture or tissue samples, and it provides a well-established model suitable for detailed studies of necroptosis molecular mechanisms in vitro.
作者: Asparagus    時(shí)間: 2025-3-27 19:41

作者: 臥虎藏龍    時(shí)間: 2025-3-28 01:17
Blutung in der Nachgeburtsperiode,orescence intensity correlated with the degree of secondary necrosis. Altogether, the measures provide exquisite kinetic resolution of dose- and agent-dependent apoptotic responses, from early through late phases. At exposure termination, other compatible reagents can be applied to measure additional orthogonal correlates of cell health.
作者: CURT    時(shí)間: 2025-3-28 04:40

作者: VERT    時(shí)間: 2025-3-28 07:48
A Real-Time, Bioluminescent Apoptosis Assay,orescence intensity correlated with the degree of secondary necrosis. Altogether, the measures provide exquisite kinetic resolution of dose- and agent-dependent apoptotic responses, from early through late phases. At exposure termination, other compatible reagents can be applied to measure additional orthogonal correlates of cell health.
作者: 起皺紋    時(shí)間: 2025-3-28 10:46

作者: Congeal    時(shí)間: 2025-3-28 17:13

作者: DEAF    時(shí)間: 2025-3-28 20:24

作者: AMBI    時(shí)間: 2025-3-29 00:16
A Triple-Parameter-Based Laboratory-Friendly Fluorescence Imaging to Identify Apoptosis in Live Celers of apoptosis. Here, we present a detailed methodology for a triple-parameter-based co-fluorescence imaging to identify apoptosis in live tumor cells. The procedure involves co-fluorescence staining specific for three cardinal features of apoptosis in live cells. The procedure is simple, time-sen
作者: 裹住    時(shí)間: 2025-3-29 04:53
Flow Cytometric Analyses of p53-Mediated Cell Cycle Arrest and Apoptosis in Cancer Cells, with DNA damaging agents. The method can be easily adapted to other genes of interest to study their contributions to the fate of variety of cell types in response to endogenous or exogenous stresses.
作者: etiquette    時(shí)間: 2025-3-29 11:03

作者: 古代    時(shí)間: 2025-3-29 12:54

作者: GRAZE    時(shí)間: 2025-3-29 16:32
1064-3745 ding known pitfalls...?Authoritative and accessible,?.Detection of Cell Death Mechanisms: Methods and Protocols?.aims to ensure seamless execution of protocols on specific cell death type..978-1-0716-1164-7978-1-0716-1162-3Series ISSN 1064-3745 Series E-ISSN 1940-6029
作者: 氣候    時(shí)間: 2025-3-29 20:37
Die biologischen Phasen im Leben des Weibes,tern blot analysis of caspase cleavage during apoptosis. We detail protocols for protein extraction, quantitation, casting, and running gel electrophoresis and western blot analysis of caspase -8 and caspase -9 activation. The described methods can be applied to any particular protein of interest.
作者: convulsion    時(shí)間: 2025-3-30 02:52
https://doi.org/10.1007/978-3-642-47656-3ers of apoptosis. Here, we present a detailed methodology for a triple-parameter-based co-fluorescence imaging to identify apoptosis in live tumor cells. The procedure involves co-fluorescence staining specific for three cardinal features of apoptosis in live cells. The procedure is simple, time-sen
作者: 并入    時(shí)間: 2025-3-30 06:23
https://doi.org/10.1007/978-3-642-47656-3 with DNA damaging agents. The method can be easily adapted to other genes of interest to study their contributions to the fate of variety of cell types in response to endogenous or exogenous stresses.
作者: chronicle    時(shí)間: 2025-3-30 10:30

作者: 乳白光    時(shí)間: 2025-3-30 14:48

作者: craving    時(shí)間: 2025-3-30 18:20
Determination and Quantitation of Cytotoxic T Cell-Mediated Cell Death,
作者: CLAY    時(shí)間: 2025-3-30 22:09

作者: 擴(kuò)張    時(shí)間: 2025-3-31 01:57
https://doi.org/10.1007/978-3-642-72089-5Bioinformatics tools and resources are valuable for the analysis of data sets focusing on programmed cell death. This chapter discusses methods for the generation of gene sets as well as enrichment analysis using publicly available databases.
作者: BRAVE    時(shí)間: 2025-3-31 07:43

作者: 征稅    時(shí)間: 2025-3-31 11:32

作者: 收集    時(shí)間: 2025-3-31 13:27

作者: harbinger    時(shí)間: 2025-3-31 17:41

作者: 領(lǐng)巾    時(shí)間: 2025-3-31 21:59
Methods in Molecular Biologyhttp://image.papertrans.cn/d/image/269205.jpg




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