標題: Titlebook: Extracellular RNA; Methods and Protocol Tushar Patel Book 2018 Springer Science+Business Media, LLC, part of Springer Nature 2018 biomarker [打印本頁] 作者: 可樂 時間: 2025-3-21 18:57
書目名稱Extracellular RNA影響因子(影響力)
書目名稱Extracellular RNA影響因子(影響力)學科排名
書目名稱Extracellular RNA網(wǎng)絡公開度
書目名稱Extracellular RNA網(wǎng)絡公開度學科排名
書目名稱Extracellular RNA被引頻次
書目名稱Extracellular RNA被引頻次學科排名
書目名稱Extracellular RNA年度引用
書目名稱Extracellular RNA年度引用學科排名
書目名稱Extracellular RNA讀者反饋
書目名稱Extracellular RNA讀者反饋學科排名
作者: COLIC 時間: 2025-3-21 20:54 作者: affect 時間: 2025-3-22 04:29 作者: 盡管 時間: 2025-3-22 06:59 作者: 某人 時間: 2025-3-22 11:23 作者: 常到 時間: 2025-3-22 15:08 作者: 常到 時間: 2025-3-22 17:02
Borel-Weil Theory for Loop Groups,her to either enrich total nsEV populations or enrich nsEVs derived from a particular tissue type from the overall nsEV population. The methods described here are compatible with parallel processing of dozens of biofluid samples and can be valuable tools for enabling nsEV analyses that have high tra作者: overbearing 時間: 2025-3-22 23:55
Infinite Dimensional Lie Algebras-protein) on the EV surface, tagged EVs may be specifically isolated using simple affinity chromatography. Moreover, recovered EVs are enriched in the tag-protein relative to the starting population of EVs and relative to EVs purified from cell culture supernatant by standard differential centrifuga作者: LEVER 時間: 2025-3-23 03:35
Infinite Dimensional Morse Theory,enewed interest in the study of plasma lipoprotein biology. This chapter describes principles and methods based on density ultracentrifugation and size exclusion chromatography for the isolation of plasma lipoproteins as a source of extracellular RNA.作者: 良心 時間: 2025-3-23 07:49 作者: 迅速飛過 時間: 2025-3-23 12:16
Isolation of Extracellular RNA from Serum/Plasma,describe protocols for commercially available kits that have been modified to yield consistent results for isolation of extracellular RNA from both whole serum/plasma and extracellular vesicle-enriched serum/plasma samples.作者: GRAVE 時間: 2025-3-23 14:42
Droplet Digital PCR for Quantitation of Extracellular RNA,eir detection are needed. Digital polymerase chain reaction (dPCR) can be a useful method for detecting and analyzing extracellular RNA. The sensitivity of digital PCR can exceed that of quantitative PCR for low abundance targets such as extracellular RNA.作者: DUST 時間: 2025-3-23 19:14 作者: 清楚 時間: 2025-3-24 00:54 作者: 領(lǐng)先 時間: 2025-3-24 03:04
Endometrial Receptivity in PCOSsolation of subpopulations of macromolecules of interest found in biofluids. Here, we introduce the protocols decision tree developed by the Extracellular RNA Communication Consortium and available on their website (exRNA portal), and compare all methods currently available to the exRNA field and report pros and cons for each platform.作者: 共棲 時間: 2025-3-24 09:11
https://doi.org/10.1007/BFb0069385describe protocols for commercially available kits that have been modified to yield consistent results for isolation of extracellular RNA from both whole serum/plasma and extracellular vesicle-enriched serum/plasma samples.作者: COUCH 時間: 2025-3-24 14:41 作者: Etching 時間: 2025-3-24 15:50
Some Examples of Linear Groups,cking. Here we describe the efficient loading of hydrophobically modified siRNAs (hsiRNAs) into EVs upon co-incubation, without altering vesicle size distribution or integrity. This method is expected to advance the development of EV-based therapies for the treatment of a broad range of disorders.作者: 誤傳 時間: 2025-3-24 19:53
Demonology: Metaphysics of (In)Fertility, applications as biomarkers and therapeutics, as well as the new challenges that arise in isolation and purification for accurate and reproducible analysis. Here we review the most recent advancements in exRNA research.作者: 膠水 時間: 2025-3-24 23:42 作者: 兇猛 時間: 2025-3-25 06:33
Infinite Group Actions on Polyhedrar preparation of small RNA libraries for NGS analysis. This protocol has been optimized for use with low-input exRNA-containing samples, such as plasma or serum, and has modifications designed to reduce the sequence-specific bias typically encountered with commercial small RNA library construction kits.作者: 注意 時間: 2025-3-25 11:34
Are Unitarizable Groups Amenable?,uids like plasma and serum using the Nanostring nCounter platform. Assays can be used to quantitate the expression of miRNA using direct detection based on hybridization to target specific color-coded probes followed by counting each color-coded barcode digitally.作者: 真 時間: 2025-3-25 14:41 作者: ferment 時間: 2025-3-25 19:52 作者: 朝圣者 時間: 2025-3-25 23:15 作者: 六個才偏離 時間: 2025-3-26 00:08
Multiplexed Detection and Quantitation of Extracellular Vesicle RNA Expression Using NanoString,uids like plasma and serum using the Nanostring nCounter platform. Assays can be used to quantitate the expression of miRNA using direct detection based on hybridization to target specific color-coded probes followed by counting each color-coded barcode digitally.作者: Eeg332 時間: 2025-3-26 07:50 作者: 不可接觸 時間: 2025-3-26 08:53
Book 2018materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls...Authoritative and cutting-edge, .Extracellular RNA: Methods and Protocols .aims to ensure successful results in the further study of this vital field.?.作者: delegate 時間: 2025-3-26 14:17 作者: DEFER 時間: 2025-3-26 18:26 作者: cocoon 時間: 2025-3-27 00:56
Detection and Analysis of Non-vesicular Extracellular RNA,onditioned media of mammalian cell culture. Focus on this fraction will increase our understanding on extracellular RNA biology, while serving as a source for biomarker discovery complementary to EVs.作者: 柏樹 時間: 2025-3-27 02:04
Milk-derived Extracellular Vesicles for Therapeutic Delivery of Small Interfering RNAs,s with RNA is possible with the use of chemical transfection reagents. This method describes the use of milk-derived EV for delivery of small interfering RNA. These EVs were shown to be taken up by hepatocellular carcinoma cells in vitro, with a reduction in the expression of target gene.作者: 預知 時間: 2025-3-27 08:03
Unsaturated Soil Hydraulic Properties,ll culture supernatants have been previously used by investigators. Here, we describe several standardized protocols for the isolation of RNAs from cell culture supernatants that utilize commercially available kits and reagents.作者: 嚴峻考驗 時間: 2025-3-27 09:33
Differential Equations with Random Delay,es of body fluids which contain protein, mRNA, and noncoding RNA. Extracellular RNA isolated from bile could be a useful tool for analyzing biliary tract diseases or cancer. Herein, we describe protocols based on modifications of commercially available kits for the collection, processing, and isolation of extracellular RNA from bile.作者: 顯而易見 時間: 2025-3-27 15:12 作者: Certainty 時間: 2025-3-27 18:29 作者: 自制 時間: 2025-3-28 01:31
Tushar PatelIncludes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts作者: DEVIL 時間: 2025-3-28 02:24 作者: 語源學 時間: 2025-3-28 06:25 作者: Loathe 時間: 2025-3-28 12:10 作者: 敵手 時間: 2025-3-28 15:17
Extracellular RNA978-1-4939-7652-2Series ISSN 1064-3745 Series E-ISSN 1940-6029 作者: 地殼 時間: 2025-3-28 22:15 作者: 有毒 時間: 2025-3-29 00:35 作者: 成績上升 時間: 2025-3-29 05:40 作者: 甜得發(fā)膩 時間: 2025-3-29 10:04 作者: gait-cycle 時間: 2025-3-29 12:26
https://doi.org/10.1007/BFb0069385 and therapeutic applications. As a newly emerging field, one of the main obstacles is the lack of standardized protocols for RNA isolations. Here we describe protocols for commercially available kits that have been modified to yield consistent results for isolation of extracellular RNA from both wh作者: Hyperplasia 時間: 2025-3-29 18:32 作者: Coterminous 時間: 2025-3-29 23:36 作者: Irrigate 時間: 2025-3-30 02:45 作者: 細頸瓶 時間: 2025-3-30 04:28 作者: CREST 時間: 2025-3-30 08:32 作者: evaculate 時間: 2025-3-30 15:15 作者: Optometrist 時間: 2025-3-30 18:47 作者: perimenopause 時間: 2025-3-30 21:50 作者: effrontery 時間: 2025-3-31 03:27
Are Unitarizable Groups Amenable?, and potential utility of these as disease biomarkers requires the ability to detect their presence with adequate sensitivity and to quantitate their expression. The potential for circulating miRNA to serve as biomarkers can be evaluated through their detection in association with specific disease s
