Titlebook: Neuroproteomics; Ka Wan Li Book 2019Latest edition Springer Science+Business Media, LLC, part of Springer Nature 2019 rodent brain regions

開(kāi)脫

書(shū)目名稱(chēng)Neuroproteomics影響因子(影響力)




書(shū)目名稱(chēng)Neuroproteomics影響因子(影響力)學(xué)科排名




書(shū)目名稱(chēng)Neuroproteomics網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱(chēng)Neuroproteomics網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱(chēng)Neuroproteomics被引頻次




書(shū)目名稱(chēng)Neuroproteomics被引頻次學(xué)科排名




書(shū)目名稱(chēng)Neuroproteomics年度引用




書(shū)目名稱(chēng)Neuroproteomics年度引用學(xué)科排名




書(shū)目名稱(chēng)Neuroproteomics讀者反饋




書(shū)目名稱(chēng)Neuroproteomics讀者反饋學(xué)科排名

傳染

Enrichment of Low-Molecular-Weight Phosphorylated Biomolecules Using Phos-Tag Tip,0 min per sample. This micropipette-tip method would be thus used preferentially as an alternative to existing tools for the reliable enrichment of phosphorylated biomolecules, such as phosphopeptides, in the field of neuroscience.

Salivary-Gland

,Integrated Immunoprecipitation: Blue Native Gel Electrophoresis—Mass Spectrometry for the Identificlexes. Here, we describe a protocol that combines the specificity of immunoprecipitation, the size separating capacity of Blue native polyacrylamide gel electrophoresis, and subsequent mass spectrometry to delineate the protein constituents in subcomplexes of a targeted protein.

加入

Apraxia

Peristalsis

High-pH Reversed-Phase Pre-Fractionation for In-Depth Shotgun Proteomics,tide mixtures, in which the HPLC-based reversed-phase fractionation provides higher resolving power while the tip-based high-pH reversed-phase fractionation is simple, parallelizable, and suitable for limited amount of biological samples.

Antagonist

,Analysis of Synaptic Protein–Protein Interaction by Cross-linking Mass Spectrometry, hybrid analysis, this protocol could characterize protein–protein interactions in a more physiological setting and allows the detection of native protein complexes contained in the mouse synaptosome.

組成

LAP

2D-DIGE as a Tool in Neuroproteomics,esis (2D-DIGE) currently being the most comprehensive technique to quantify these changes while retaining information about isoforms and posttranslational modifications. This chapter focusses on technical aspects of 2D-DIGE as well as a brief overview of successful applications of this technique in neuroproteomics.

凌辱

A Combined Cellomics and Proteomics Approach to Uncover Neuronal Pathways to Psychiatric Disorder,ctional pathways and interactome connections of selected risk genes. The overlay of pathway and proteome data from selected genes in a biological context can be used to formulate new testable hypothesis of both the genetics and the biology of the disorders.