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Human neural culture on a chip recapitulates neuron–glia interactions.
The cover shows a 3D human neural culture on a chip, which allows the engagement of neurons with only disease-associated microglia, and their separation out from a heterogeneous microglia population. The image shows membrane-labeled microglia (red), GFP-labeled neuron and astrocyte (yellow), and immunostaining for astrocyte marker GFAP (blue). See Kang et al. p2838.
Image: You Jung Kang, Yen N. Diep and Hansang Cho, Sungkyunkwan University. Cover design: S. Whitham.
This tutorial provides guidelines for imputing human leukocyte antigen alleles, including standard quality control measures for input genotyping data and best practice recommendations for association testing and fine-mapping to identify causal alleles.
This protocol for universal and proficient Pseudomonas recombineering uses phage-encoded homologous recombination–Cas3 systems, including SacB counterselection and Cre site-specific recombinase for two- or three-step seamless genome modification.
This protocol is for using CapQuant, a mass spectrometry-based technique for accurate and sensitive quantification of the epitranscriptome of RNA caps using stable isotope-labeled cap nucleotides.
The authors provide a detailed protocol for the isolation of four membrane protein complexes (transmembrane channel-like proteins 1 and 2, lipid transfer protein and ‘Protein S’) from transgenic C. elegans.
Combining surface-enhanced Raman spectroscopy with surface-accessible nanomaterials allows molecule–metal interactions to be probed in the complex environments that are directly relevant to their application. This will underpin the development of improved functional nanomaterials.
This protocol describes how to measure the rate of racemization in atropisomers by (i) kinetic analysis of the racemization of an enantioenriched sample, (ii) dynamic HPLC and (iii) variable-temperature NMR.
A protocol for setting up, calibrating and validating a semi-automated sample processing pipeline for cell-free RNA isolation from clinical samples using the Opentrons 1.0 or 2.0 open-source robotic platform.
The authors provide a protocol for cytosine base editing to introduce precise substitutions into the genome of zebrafish, an important model for genetic studies and in vivo disease modeling.
In this protocol, layered semiconductor crystals undergo electrochemical intercalation of organic cations followed by exfoliation to form 2D nanosheets in solution. These nanosheets can assemble into thin films for diverse electronic applications.
Protocol for the fabrication of a microfluidic device and its implementation in three-dimensional human neural cultures, allowing the study of neuron–glia interactions in neuroinflammation and neurodegeneration.