Nanobody-based 3D immunohistochemistry allows rapid visualization in thick tissue samples
Peer-Reviewed Publication
Updates every hour. Last Updated: 16-Aug-2025 13:11 ET (16-Aug-2025 17:11 GMT/UTC)
Three dimensional immunohistochemistry (3D-IHC) reveals spatial and molecular details of biological tissues, but current methods are slow and limited in depth. Researchers from Japan have developed a fast, high-sensitivity 3D-IHC method using nanobodies fused with peroxidase and a novel signal amplification system. Their technique labels neurons and glia in 1-mm-thick brain tissue within three days, offering a powerful new tool for neuroscience and disease research, including Alzheimer’s pathology.
A novel time-division MIMO technology enables phased-array receivers to operate faster with exceptional area efficiency and low power, as reported by researchers from Institute of Science Tokyo. The proposed system significantly reduces circuit complexity for 5G and 6G networks, including non-terrestrial nodes, by reusing signal paths through fast switching. It demonstrated a record-setting 38.4 Gbps data rate across eight streams in a 65 nm CMOS integrated circuit.
A research team from The University of Osaka and Institute of Science Tokyo has developed a groundbreaking class of mRNA medicines that can sense changes in the body and autonomously adjust their therapeutic effect. This innovation paves the way for precision treatments that are not only more effective, but also safer—by producing just the right amount of medicine based on real-time biological signals.
Researchers from The University of Osaka found that Oxr1 and Ncoa7 regulate the vacuolar-type proton pump ATPase on the membrane of the Golgi apparatus and trans-Golgi network to maintain their luminal pH. Inhibition of Oxr1 and Ncoa7 function disrupts glycosylation, a key enzymatic process that takes place in these organelles, providing new insight into the mechanisms underlying congenital disorders of glycosylation.
A research team at The University of Osaka has unveiled the molecular mechanism behind genome ejection from adeno-associated virus (AAV) vectors, a crucial delivery vehicle in gene therapy. The study reveals that the N-terminal region of the VP1 protein, a component of the AAV capsid, undergoes structural changes upon heating, facilitating the release of the therapeutic genetic material. This discovery offers new guidelines for vector design and stability assessment, promising more efficient and safer gene therapies.
Excitons--bound pairs of electrons and holes created by light--are key to the optoelectronic behavior of carbon nanotubes (CNTs). However, because excitons are confined to extremely small regions and exist for only fleeting moments, it has been extremely challenging to directly observe their behavior using conventional measurement techniques.
In this study, we overcame that challenge by using an ultrafast infrared near-field optical microscope that focuses femtosecond infrared laser pulses down to the nanoscale. This advanced approach allowed us to visualize where excitons are generated and decay inside CNTs in real space and real time.
Our observations revealed that nanoscale variations in the local environment--such as subtle lattice distortions within individual CNTs or interactions with neighboring CNTs--can significantly affect exciton generation and relaxation dynamics.
These insights into local exciton dynamics pave the way for precise control of light-matter interactions at the nanoscale, offering new opportunities for the development of advanced optoelectronic devices and quantum technologies based on carbon nanotube platforms.