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標(biāo)題: Titlebook: Chromatin Immunoprecipitation; Methods and Protocol Neus Visa,Antonio Jordán-Pla Book 2018 Springer Science+Business Media LLC 2018 ChIP as [打印本頁(yè)]

作者: 爆裂    時(shí)間: 2025-3-21 18:16
書目名稱Chromatin Immunoprecipitation影響因子(影響力)




書目名稱Chromatin Immunoprecipitation影響因子(影響力)學(xué)科排名




書目名稱Chromatin Immunoprecipitation網(wǎng)絡(luò)公開度




書目名稱Chromatin Immunoprecipitation網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Chromatin Immunoprecipitation被引頻次




書目名稱Chromatin Immunoprecipitation被引頻次學(xué)科排名




書目名稱Chromatin Immunoprecipitation年度引用




書目名稱Chromatin Immunoprecipitation年度引用學(xué)科排名




書目名稱Chromatin Immunoprecipitation讀者反饋




書目名稱Chromatin Immunoprecipitation讀者反饋學(xué)科排名





作者: 是剝皮    時(shí)間: 2025-3-22 00:08

作者: Cpr951    時(shí)間: 2025-3-22 02:04

作者: 寬容    時(shí)間: 2025-3-22 08:10

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作者: palliative-care    時(shí)間: 2025-3-22 14:28

作者: palliative-care    時(shí)間: 2025-3-22 18:57
978-1-4939-8467-1Springer Science+Business Media LLC 2018
作者: 陰郁    時(shí)間: 2025-3-22 23:37

作者: CLEFT    時(shí)間: 2025-3-23 02:45
History of Mechanism and Machine Scienceional regulation. Here, we describe a process to analyze bacterial transcription factor binding in the context of an infected eukaryotic host cell. Using this approach, we measured the binding kinetics of three . transcription factors within infected cells, and demonstrated temporal changes in binding.
作者: Obsessed    時(shí)間: 2025-3-23 06:04

作者: 業(yè)余愛好者    時(shí)間: 2025-3-23 12:40

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作者: 填料    時(shí)間: 2025-3-23 20:47
Reconstructing the Work of Teacher Educatorsd forms of proteins and a genomic DNA region. Combined with genome-wide profiling technologies, such as microarray hybridization (ChIP-on-chip) or massively parallel sequencing (ChIP-seq), ChIP could provide a genome-wide mapping of in vivo protein–DNA interactions in various organisms. Here, we des
作者: Saline    時(shí)間: 2025-3-24 01:30

作者: Fabric    時(shí)間: 2025-3-24 04:40

作者: 傳授知識(shí)    時(shí)間: 2025-3-24 08:25

作者: interpose    時(shí)間: 2025-3-24 11:02
Jeanine Gallagher,Jill Willis,Nerida Spinar formaldehyde fixed chromatin is subjected to digestion by micrococcal nuclease (MNase), which degrades linker DNA and yields mainly mono-nucleosomes. The resulting material can be processed directly or can be subjected to an optional chromatin immunoprecipitation step (MNase-ChIP-seq). De-crosslin
作者: menopause    時(shí)間: 2025-3-24 15:36
,Su Song’s Escapement Regulator,e of experimental parameters. A number of proteins bound at the same genomic location can identify a multi-protein chromatin complex where several proteins work together to regulate gene transcription or chromatin configuration. In many instances, this can be achieved using sequential ChIP; or simpl
作者: dandruff    時(shí)間: 2025-3-24 21:01
History of Mechanism and Machine Sciencef epigenetic complexes within cells remain incompletely understood, partly due to technical challenges. Here, we present a new approach termed single-molecule chromatin immunoprecipitation imaging (Sm-ChIPi) that enables to assess the cellular assembly stoichiometry of epigenetic complexes on chroma
作者: MILL    時(shí)間: 2025-3-24 23:12
History of Mechanism and Machine Scienceional regulation using antibodies to enrich genomic regions associated with these epitopes. Either to monitor the presence of histones with post-translational modifications at specific genomic locations or to measure transcription factor interactions with a candidate target gene, protein–DNA complex
作者: Confess    時(shí)間: 2025-3-25 06:14
https://doi.org/10.1007/978-1-4020-6460-9al intracellular processes such as DNA replication, transcription regulation, chromatin stability, and others are all dependent on protein interactions with DNA. The DNA fragments enriched from the ChIP assay are analyzed by downstream applications, for example, microarray hybridization (ChIP-chip),
作者: 不給啤    時(shí)間: 2025-3-25 11:00

作者: BIDE    時(shí)間: 2025-3-25 13:45

作者: cloture    時(shí)間: 2025-3-25 16:51
https://doi.org/10.1007/978-1-4020-6460-9cription factor binding sites and histone chemical modifications. However, these approaches only allow profiling of a single factor or protein modification at a time..In this chapter, we present Bar-ChIP, a higher throughput version of ChIP-Seq that relies on the direct ligation of molecular barcode
作者: 隱語(yǔ)    時(shí)間: 2025-3-25 21:16

作者: maculated    時(shí)間: 2025-3-26 00:39

作者: Lineage    時(shí)間: 2025-3-26 06:18

作者: cornucopia    時(shí)間: 2025-3-26 12:10
Considerations on Experimental Design and Data Analysis of Chromatin Immunoprecipitation Experimentteins and genomic DNA. Ever since its inception, more than 30 years ago, ChIP has been constantly evolving, improving, and expanding its capabilities and reach. Despite its widespread use by many laboratories across a wide variety of disciplines, ChIP assays can be sometimes challenging to design, a
作者: 啤酒    時(shí)間: 2025-3-26 15:37

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作者: AWE    時(shí)間: 2025-3-26 21:05
Chromatin Immunoprecipitation from Mouse Embryonic Tissue or Adherent Cells in Culture, Followed byomic regions. It is of paramount importance in gene-regulation studies, as it can be used to map the target regions of sequence-specific transcription factors and cofactors, or histone marks that characterize distinct chromatin states. ChIP can be used directly to probe interactions with candidate r
作者: 出血    時(shí)間: 2025-3-27 01:22
Chromatin RNA Immunoprecipitation (ChRIP),mulated evidence suggests lncRNAs could act as interphase molecules between chromatin and chromatin remodelers to define the epigenetic code. However, it is not clear how lncRNAs target chromatin remodelers to specific chromosomal regions in order to establish a functionally distinct epigenetic stat
作者: GIST    時(shí)間: 2025-3-27 06:21
DNA Accessibility by MNase Digestions,tected fragments can then be analyzed by genome-wide sequencing techniques or by quantitative PCR to obtain information about the positions of nucleosomes in the chromatin. Nucleosomes are differentially sensitive to MNase digestion, which means that titrations of MNase should be performed to obtain
作者: 結(jié)合    時(shí)間: 2025-3-27 11:44
Characterization of the Nucleosome Landscape by Micrococcal Nuclease-Sequencing (MNase-seq),r formaldehyde fixed chromatin is subjected to digestion by micrococcal nuclease (MNase), which degrades linker DNA and yields mainly mono-nucleosomes. The resulting material can be processed directly or can be subjected to an optional chromatin immunoprecipitation step (MNase-ChIP-seq). De-crosslin
作者: 使尷尬    時(shí)間: 2025-3-27 14:41
ChIP-re-ChIP: Co-occupancy Analysis by Sequential Chromatin Immunoprecipitation,e of experimental parameters. A number of proteins bound at the same genomic location can identify a multi-protein chromatin complex where several proteins work together to regulate gene transcription or chromatin configuration. In many instances, this can be achieved using sequential ChIP; or simpl
作者: Fissure    時(shí)間: 2025-3-27 20:39

作者: watertight,    時(shí)間: 2025-3-28 01:17
Chromatin Immunoprecipitation of Skeletal Muscle Tissue,ional regulation using antibodies to enrich genomic regions associated with these epitopes. Either to monitor the presence of histones with post-translational modifications at specific genomic locations or to measure transcription factor interactions with a candidate target gene, protein–DNA complex
作者: STERN    時(shí)間: 2025-3-28 05:56

作者: peritonitis    時(shí)間: 2025-3-28 08:40
,Using Intra-ChIP to Measure Protein–DNA Interactions in Intracellular Pathogens,ional regulation. Here, we describe a process to analyze bacterial transcription factor binding in the context of an infected eukaryotic host cell. Using this approach, we measured the binding kinetics of three . transcription factors within infected cells, and demonstrated temporal changes in bindi
作者: Hamper    時(shí)間: 2025-3-28 12:11

作者: airborne    時(shí)間: 2025-3-28 16:03

作者: FLAG    時(shí)間: 2025-3-28 20:47
Analysis of ChIP-seq Data in R/Bioconductor,egulation in multiple conditions at unprecedented resolution and scale. Proactive quality-control and appropriate data analysis techniques are of critical importance to extract the most meaningful results from the data. Over the last years, an array of R/Bioconductor tools has been developed allowin
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作者: 我正派    時(shí)間: 2025-3-29 13:22
https://doi.org/10.1007/978-1-4020-6460-9ional analyses to annotate regulatory regions. The steps in the data analysis process were demonstrated on publicly available data sets and will serve as a demonstration of the computational procedures routinely used for the analysis of ChIP-seq data in R/Bioconductor, from which readers can constru
作者: Intruder    時(shí)間: 2025-3-29 17:16

作者: CLAY    時(shí)間: 2025-3-29 19:46
1064-3745 iques, including bioinformatic analysis of ChIP data, will be of interest to a very broad research community in the fields of biochemistry, molecular biology, microbiology, and biomedicine..978-1-4939-8467-1978-1-4939-7380-4Series ISSN 1064-3745 Series E-ISSN 1940-6029
作者: 悠然    時(shí)間: 2025-3-30 01:56

作者: Irremediable    時(shí)間: 2025-3-30 07:03

作者: 威脅你    時(shí)間: 2025-3-30 12:05
Analysis of ChIP-seq Data in R/Bioconductor,ional analyses to annotate regulatory regions. The steps in the data analysis process were demonstrated on publicly available data sets and will serve as a demonstration of the computational procedures routinely used for the analysis of ChIP-seq data in R/Bioconductor, from which readers can constru
作者: 吝嗇性    時(shí)間: 2025-3-30 13:51

作者: 磨坊    時(shí)間: 2025-3-30 18:02

作者: Abrupt    時(shí)間: 2025-3-30 23:19

作者: 慎重    時(shí)間: 2025-3-31 04:29
Considerations on Experimental Design and Data Analysis of Chromatin Immunoprecipitation Experimentsign and perform experiments that generate the most reproducible, high-quality data. Some of the main topics covered include the use of properly characterized antibodies, alternatives to chromatin preparation, the need for proper controls, and some recommendations about ChIP-seq data analysis.
作者: 喚起    時(shí)間: 2025-3-31 05:19

作者: 蘑菇    時(shí)間: 2025-3-31 12:10
Jeanine Gallagher,Jill Willis,Nerida Spinadscape in the malaria parasite, ., but most steps are directly applicable to other cell types. We also discuss general considerations for experimental design and computational analysis, which are crucial for accurate investigation of the nucleosome landscape.
作者: 畏縮    時(shí)間: 2025-3-31 14:21
History of Mechanism and Machine Sciencel scale and under low background conditions. Here, we describe the procedure in the study of transcription factors in the model plant .. However, with some modifications, the technique should also be implemented in other systems. Besides cell type-specific studies, MOBE-ChIP can also be used as a general strategy to improve ChIP signals.
作者: 表皮    時(shí)間: 2025-3-31 20:04
Chromatin RNA Immunoprecipitation (ChRIP), inactive chromatin compartments. Use of ChRIP to identify chromatin-bound lncRNA will further improve our knowledge regarding the functional role of lncRNAs in establishing epigenetic modifications of chromatin.
作者: Esalate    時(shí)間: 2025-3-31 22:17
Characterization of the Nucleosome Landscape by Micrococcal Nuclease-Sequencing (MNase-seq),dscape in the malaria parasite, ., but most steps are directly applicable to other cell types. We also discuss general considerations for experimental design and computational analysis, which are crucial for accurate investigation of the nucleosome landscape.
作者: Pantry    時(shí)間: 2025-4-1 02:52





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