標(biāo)題: Titlebook: Environmental Microbiology; Methods and Protocol Ian T. Paulsen,Andrew J. Holmes Book 2014Latest edition Springer Science+Business Media, L [打印本頁(yè)] 作者: FARCE 時(shí)間: 2025-3-21 16:08
書(shū)目名稱(chēng)Environmental Microbiology影響因子(影響力)
作者: 品嘗你的人 時(shí)間: 2025-3-21 21:32
Biolog Phenotype MicroArrays for Phenotypic Characterization of Microbial Cellsgle microorganisms and for physiological profiling of bacterial communities. The microplate system can be used to obtain a comprehensive overview of metabolic capability, or it can be tailored, through the use of subsets of plates, to address specific research needs.作者: 使人煩燥 時(shí)間: 2025-3-22 04:03 作者: 柏樹(shù) 時(shí)間: 2025-3-22 05:54 作者: dainty 時(shí)間: 2025-3-22 10:19 作者: LITHE 時(shí)間: 2025-3-22 16:52
,The Reform of ‘Checkout Data’, plates, shake flasks, and bench top fermenters starting with an inoculum that typically features fungal spores. Here we discuss the most popular methods for the isolation and cultivation of filamentous fungi for various purposes with the emphasis on enzyme production and molecular microbiology.作者: LITHE 時(shí)間: 2025-3-22 21:06 作者: 項(xiàng)目 時(shí)間: 2025-3-22 23:27 作者: THE 時(shí)間: 2025-3-23 03:46
Susan K. Foley,Charles Sowerwinepollution in ambient water samples. The following protocol includes water sample collection, filtration, DNA isolation with a sample processing control, qPCR amplification with an internal amplification control, and quality control data analysis.作者: 別炫耀 時(shí)間: 2025-3-23 08:15
A Political Sociology of Regionalismshe identification of unculturable or rare organisms within a sample. Multiplexing can be used to sequence multiple samples in tandem through the use of sample-specific identification sequences which are attached to each amplicon, making this a cost-effective method for large-scale microbial identification experiments.作者: 長(zhǎng)處 時(shí)間: 2025-3-23 13:15
Conclusion: For Unto Us Post-truth Is Born,hput, semiquantitative analysis of the major methanotroph groups in a number of different environments..Here we describe the use of a .-based short oligo array for the analysis of methanotroph populations in sediment samples. The method is suitable for analysis of any type of environmental sample from which DNA can be extracted.作者: lipoatrophy 時(shí)間: 2025-3-23 16:38
Book 2014Latest edition Microbiology: Methods and Protocols. looks at recent advances that are having a big impact on the field such as metagenomics and other “omics” technologies, NanoSIMS, as well as stable isotope probing and more.?Conveniently divided into four parts, the first section looks at methods involved in sam作者: certitude 時(shí)間: 2025-3-23 19:29
Despina Moraitou,Anastasia Efklidescommunity. We outline the considerations and analyses that should be undertaken to ensure the success of a metagenomic sequencing project, including the choice of sequencing platform and methods for assembly, binning, annotation, and comparative analysis.作者: ANN 時(shí)間: 2025-3-24 02:04 作者: FLAG 時(shí)間: 2025-3-24 05:55 作者: Fluctuate 時(shí)間: 2025-3-24 07:13 作者: Anthropoid 時(shí)間: 2025-3-24 14:38
Terminal Restriction Fragment Length Polymorphism (T-RFLP) Profiling of Bacterial 16S rRNA Genesof the dominant members of a bacterial community, by PCR amplification of the bacterial 16S rRNA genes and three restriction endonuclease digests to generate three different profiles for each sample. The generation of multiple profiles per sample provides enough information to confidently differentiate rich environmental bacterial communities.作者: 確認(rèn) 時(shí)間: 2025-3-24 18:54
Human Fecal Source Identification with Real-Time Quantitative PCRpollution in ambient water samples. The following protocol includes water sample collection, filtration, DNA isolation with a sample processing control, qPCR amplification with an internal amplification control, and quality control data analysis.作者: LEVY 時(shí)間: 2025-3-24 21:37 作者: endarterectomy 時(shí)間: 2025-3-25 02:22 作者: –吃 時(shí)間: 2025-3-25 06:06 作者: 鄙視讀作 時(shí)間: 2025-3-25 08:24 作者: 作繭自縛 時(shí)間: 2025-3-25 12:51 作者: Hectic 時(shí)間: 2025-3-25 17:25 作者: Visual-Field 時(shí)間: 2025-3-25 21:56 作者: 創(chuàng)新 時(shí)間: 2025-3-26 03:44
Environmental Microbiology978-1-62703-712-9Series ISSN 1064-3745 Series E-ISSN 1940-6029 作者: 難聽(tīng)的聲音 時(shí)間: 2025-3-26 05:47 作者: GREG 時(shí)間: 2025-3-26 10:31 作者: 聽(tīng)寫(xiě) 時(shí)間: 2025-3-26 16:15 作者: 徹底明白 時(shí)間: 2025-3-26 20:33 作者: Host142 時(shí)間: 2025-3-26 23:53
https://doi.org/10.1007/978-3-030-50049-8 such analyses is the efficient and representative recovery of PCR-competent DNA from complex environmental samples. All extraction protocols contain inherent biases, meaning that choice of method involves compromise between various factors, including efficiency, yield, universality, and representat作者: 酷熱 時(shí)間: 2025-3-27 02:13
The Golden Age of the Swedish Sport Model,ation costs, this method is routinely applied in modern molecular bioscience laboratories. Nonetheless, all quantitative PCR experiments must include several carefully designed, yet simple, controls to ensure the reliability of the analyses. The aim of this chapter is to provide basic quantitative P作者: 百靈鳥(niǎo) 時(shí)間: 2025-3-27 06:22
A Political History of the Two Irelandssity can be generated in a sensitive, reproducible, and cost-effective manner. This protocol describes the steps required to generate T-RFLP profiles of the dominant members of a bacterial community, by PCR amplification of the bacterial 16S rRNA genes and three restriction endonuclease digests to g作者: Foregery 時(shí)間: 2025-3-27 11:00
Susan K. Foley,Charles Sowerwineial. We describe a real-time quantitative PCR (qPCR) method that targets a genetic marker of the human-associated . for identification of human fecal pollution in ambient water samples. The following protocol includes water sample collection, filtration, DNA isolation with a sample processing contro作者: Deadpan 時(shí)間: 2025-3-27 16:25 作者: Generic-Drug 時(shí)間: 2025-3-27 21:44
Conclusion: For Unto Us Post-truth Is Born,ant carbon source. The development and application of a microarray targeting the particulate methane monooxygenase gene (.) have allowed a high-throughput, semiquantitative analysis of the major methanotroph groups in a number of different environments..Here we describe the use of a .-based short ol作者: Osteoarthritis 時(shí)間: 2025-3-28 01:41
Assessing the theoretical approach,imetric reaction that is indicative of respiration, these microplate assays measure the response of an individual strain or microbial community to a large and diverse range of nutrients and chemicals. Phenotype MicroArrays have been used to study gene function and to improve genome annotation in sin作者: exclamation 時(shí)間: 2025-3-28 04:56 作者: 含糊 時(shí)間: 2025-3-28 09:21
https://doi.org/10.1007/978-1-349-08277-3nctions as a metabolic “fingerprint” of an individual cell, which enables differentiation of cell types, physiological states, nutrient condition, and variable phenotypes. Raman tweezers combines single-cell Raman spectroscopy with optical laser tweezers to allow the identification and isolation of 作者: CURB 時(shí)間: 2025-3-28 12:37 作者: scrutiny 時(shí)間: 2025-3-28 17:09 作者: 條約 時(shí)間: 2025-3-28 19:57 作者: 細(xì)胞學(xué) 時(shí)間: 2025-3-29 02:48
Ian T. Paulsen,Andrew J. HolmesProvides up-to-date molecular techniques for investigating microbial communities and their biological activities.Includes step-by-step, readily reproducible protocols.Features key tips and expert impl作者: capsule 時(shí)間: 2025-3-29 06:42 作者: abject 時(shí)間: 2025-3-29 08:47
1064-3745 cessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. .Fully updated and authoritative, .Environmental Microbiology: M978-1-4939-5903-7978-1-62703-712-9Series ISSN 1064-3745 Series E-ISSN 1940-6029 作者: tattle 時(shí)間: 2025-3-29 11:45 作者: 大廳 時(shí)間: 2025-3-29 16:30 作者: overrule 時(shí)間: 2025-3-29 23:10 作者: 是比賽 時(shí)間: 2025-3-30 01:01 作者: constitutional 時(shí)間: 2025-3-30 05:48
Book 2014Latest edition, and, as such, chapters contain introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. .Fully updated and authoritative, .Environmental Microbiology: M作者: Confess 時(shí)間: 2025-3-30 08:27 作者: artifice 時(shí)間: 2025-3-30 14:45 作者: JIBE 時(shí)間: 2025-3-30 17:44
Quantitative PCR for Detection of mRNA and gDNA in Environmental Isolatesation costs, this method is routinely applied in modern molecular bioscience laboratories. Nonetheless, all quantitative PCR experiments must include several carefully designed, yet simple, controls to ensure the reliability of the analyses. The aim of this chapter is to provide basic quantitative P作者: Hangar 時(shí)間: 2025-3-30 21:56
Terminal Restriction Fragment Length Polymorphism (T-RFLP) Profiling of Bacterial 16S rRNA Genessity can be generated in a sensitive, reproducible, and cost-effective manner. This protocol describes the steps required to generate T-RFLP profiles of the dominant members of a bacterial community, by PCR amplification of the bacterial 16S rRNA genes and three restriction endonuclease digests to g作者: 使出神 時(shí)間: 2025-3-31 03:32 作者: 諷刺滑稽戲劇 時(shí)間: 2025-3-31 05:23 作者: Console 時(shí)間: 2025-3-31 12:01 作者: libertine 時(shí)間: 2025-3-31 15:46
Biolog Phenotype MicroArrays for Phenotypic Characterization of Microbial Cellsimetric reaction that is indicative of respiration, these microplate assays measure the response of an individual strain or microbial community to a large and diverse range of nutrients and chemicals. Phenotype MicroArrays have been used to study gene function and to improve genome annotation in sin作者: 推崇 時(shí)間: 2025-3-31 18:18
