標(biāo)題: Titlebook: Analytics of Protein-DNA Interactions; Harald Seitz Book 2007 Springer-Verlag Berlin Heidelberg 2007 Biochemistry.Biotechnology.DNA.Microa [打印本頁(yè)] 作者: 解毒藥 時(shí)間: 2025-3-21 18:52
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書(shū)目名稱(chēng)Analytics of Protein-DNA Interactions讀者反饋
書(shū)目名稱(chēng)Analytics of Protein-DNA Interactions讀者反饋學(xué)科排名
作者: 冷漠 時(shí)間: 2025-3-21 22:57
,Analysis of Protein–DNA Interactions Using Surface Plasmon Resonance,tudied using genetic, biochemical, and structuralmethods resulting in qualitative or semiquantitative interaction data. In the future the focus will beon high quality quantitative data to model a?huge number of interactions forming a?specific networkin system biology approaches..Toward this aim, BIA作者: 障礙 時(shí)間: 2025-3-22 02:36 作者: Badger 時(shí)間: 2025-3-22 06:06
,Protein Binding Microarrays for the Characterization of DNA–Protein Interactions,y DNA binding proteins. Of particular interestare transcription factors (TFs) which, through their sequence-specific interactions with DNA binding sites,modulate gene expression in a?manner required for normal cellular growth and differentiation, and alsofor response to environmental stimuli. Despit作者: ALIAS 時(shí)間: 2025-3-22 10:08
,Accuracy and Reproducibility of Protein–DNA Microarray Technology,t technologies in this field. Protein–DNAmicroarrays utilise chips upon which a?large number of DNA sequences may be printed or synthesised.Any DNA-binding protein may then be interrogated by applying either purified sample or cellular/nuclearextracts, subject to availability of a?suitable detection作者: 隱士 時(shí)間: 2025-3-22 16:22 作者: arthrodesis 時(shí)間: 2025-3-22 19:05
Ayman Massaoudi,Noura Sellami,Mohamed Sialaexclusively in CpG dinucleotides. While the bulk ofhuman genomic DNA is depleted in CpG sites, there are CpG-rich stretches, so-called CpG islands, which arelocated in promoter regions of more than 70% of all known human genes. In normal cells, CpG islands areunmethylated, reflecting an transcriptio作者: Urgency 時(shí)間: 2025-3-23 00:58
Ayman Massaoudi,Noura Sellami,Mohamed Sialatudied using genetic, biochemical, and structuralmethods resulting in qualitative or semiquantitative interaction data. In the future the focus will beon high quality quantitative data to model a?huge number of interactions forming a?specific networkin system biology approaches..Toward this aim, BIA作者: 疲憊的老馬 時(shí)間: 2025-3-23 04:07 作者: Silent-Ischemia 時(shí)間: 2025-3-23 06:36 作者: overture 時(shí)間: 2025-3-23 10:48 作者: 向前變橢圓 時(shí)間: 2025-3-23 15:08
Thomas Lavigne,Bacem Mbarek,Tomá? Pitnerrs, by the use of mass spectrometric techniques hundreds ofpreviously unknown proteins have been identified as DNA-binding proteins that are involved in the regulationof gene expression, replication, or DNA repair. Beyond this task, the applications of mass spectrometrycover all aspects from sequenc作者: 清晰 時(shí)間: 2025-3-23 21:35
https://doi.org/10.1007/978-3-540-48150-8Biochemistry; Biotechnology; DNA; Microarray; Proteins; biology; chemistry; genetic engineering作者: overhaul 時(shí)間: 2025-3-24 02:05
978-3-642-08007-4Springer-Verlag Berlin Heidelberg 2007作者: 泄露 時(shí)間: 2025-3-24 04:44
Harald SeitzCovers trends in modern biotechnology.All aspects of this interdisciplinary technology, where knowledge, methods and expertise are required from chemistry, biochemistry, microbiology, genetics, chemic作者: Nonconformist 時(shí)間: 2025-3-24 06:47
Advances in Biochemical Engineering/Biotechnologyhttp://image.papertrans.cn/a/image/156720.jpg作者: 圓桶 時(shí)間: 2025-3-24 12:35 作者: Ablation 時(shí)間: 2025-3-24 17:57 作者: 打擊 時(shí)間: 2025-3-24 19:18
Ayman Massaoudi,Noura Sellami,Mohamed Sialade polymorphism. Eventhough different approaches have been established for analysing DNA methylation, so far detection methodsthat are capable of surveying the methylation status of multiple gene promoters have been restricted toa?limited number of cytosines. The use of oligonucleotide microarrays p作者: 幻想 時(shí)間: 2025-3-25 00:05
Ayman Massaoudi,Noura Sellami,Mohamed Siala, and finishing with extensive informationon quantitative and qualitative data analysis. One focus is on cooperative protein–DNA interactions,where proteins interact with each other to modulate their binding specificity or affinity. The BIAcorehas been used for the last 14?years to study protein–DNA作者: anthesis 時(shí)間: 2025-3-25 03:58 作者: vasospasm 時(shí)間: 2025-3-25 09:58
Chahrazed Ksouri,Abdelfettah Belghithce specificities of TFs, other DNA binding proteins, or synthetic compounds. DNA bindingsite data from PBMs combined with gene annotation data, comparative sequence analysis, and gene expressionprofiling, can be used to predict what genes are regulated by a?given TF, what the functions are ofa?given作者: modish 時(shí)間: 2025-3-25 15:41 作者: 過(guò)分 時(shí)間: 2025-3-25 19:02
Monitoring Methylation Changes in Cancer,de polymorphism. Eventhough different approaches have been established for analysing DNA methylation, so far detection methodsthat are capable of surveying the methylation status of multiple gene promoters have been restricted toa?limited number of cytosines. The use of oligonucleotide microarrays p作者: 行為 時(shí)間: 2025-3-25 20:10 作者: transplantation 時(shí)間: 2025-3-26 04:06 作者: Genteel 時(shí)間: 2025-3-26 05:31
,Protein Binding Microarrays for the Characterization of DNA–Protein Interactions,ce specificities of TFs, other DNA binding proteins, or synthetic compounds. DNA bindingsite data from PBMs combined with gene annotation data, comparative sequence analysis, and gene expressionprofiling, can be used to predict what genes are regulated by a?given TF, what the functions are ofa?given作者: 無(wú)畏 時(shí)間: 2025-3-26 11:54
Identification and Characterization of DNA-Binding Proteins by Mass Spectrometry,epertoire of mass spectrometric methods that arenow available for the identification and detailed characterization of DNA-binding proteins. These techniques,how they work, what their requirements and limitations are, and selected examples that document their performanceare described and discussed in作者: 性冷淡 時(shí)間: 2025-3-26 15:58
https://doi.org/10.1007/978-3-030-99004-6 feature, enabling relative affinities to be calculated. Keyfactors for reproducible and accurate quantification of protein binding are: microarray surface chemistry;length of oligonucleotides; position of the binding site sequence; quality of the protein and antibodies;and hybridisation conditions.作者: NOTCH 時(shí)間: 2025-3-26 20:18 作者: LATE 時(shí)間: 2025-3-27 00:56
9樓作者: 的事物 時(shí)間: 2025-3-27 01:45
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9樓作者: 圣歌 時(shí)間: 2025-3-27 11:08
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10樓作者: Original 時(shí)間: 2025-3-28 00:41
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