In the present report, we have described a method for labeling mAbs with the long-lived positron emitter Zr using the novel bifunctional chelate Df-Bz-NCS.
Because the cytokine response profile is governed by the structure of the glycolipid, we sought a method for labeling various glycolipids to study their in vivo behavior.
To examine whether lineage-based rules contribute to functional circuit organization in the optic tectum, we developed a method for labeling a single neuronal clone per animal, which enabled us to definitively identify sister tectal neurons.
To investigate the cellular behavior of different CD1d agonists, we sought a method for labeling glycolipids, which would allow us to study the mechanisms that control their uptake by professional antigen-presenting cells (APC).
In this work, we present a method for label-free, functionalization-free, selective and enhanced detection of monolayers of different bacteria using THz radiation.
Grewal et al. presented a method for label-free electrochemical detection of a protein from the enteric pathogen Entamoeba histolytica using cell-free yeast embedded antibody-like fragments (yeast-scFv) as novel affinity agents.
This project is investigating the migration and effects of rat neural precursor cells on ischaemic brain lesions using an improved method for labelling these cells in vivo using an iron based marker.
Herein, we describe a synthetic method for labeling peptides with a modular 18F/19F-labeling 18F/19F-labelingng the fast and raprotocolgn of multiple opticallowingabeled pepthees with just one radio-labeled synthetic intermediate.
