sample review
  • recombinant hevin protein was used for immunocytochemistry, in order to demonstrate the role of astrocyte-secreted protein hevin in thalamocortical synaptic connectivity in the mouse cortex
  • Alexa 488 Hydrazide was used for electrophysiological study, in order to demonstrate the role of astrocyte-secreted protein hevin in thalamocortical synaptic connectivity in the mouse cortex
  • SDS-PAGE buffer was used for immunoassay, in order to demonstrate the role of astrocyte-secreted protein hevin in thalamocortical synaptic connectivity in the mouse cortex
  • micro BCA protein assay kit was used for immunoassay, in order to demonstrate the role of astrocyte-secreted protein hevin in thalamocortical synaptic connectivity in the mouse cortex
  • NP-40 was used for immunoassay, in order to demonstrate the role of astrocyte-secreted protein hevin in thalamocortical synaptic connectivity in the mouse cortex
  • Secondary Alexa-fluorophore conjugated antibody was used for immunoassay, in order to demonstrate the role of astrocyte-secreted protein hevin in thalamocortical synaptic connectivity in the mouse cortex
  • Anti-PSD95 antibody was used for immunoassay, in order to demonstrate the role of astrocyte-secreted protein hevin in thalamocortical synaptic connectivity in the mouse cortex
  • 96-well Polysorp microtiter plate was used for ELISA, in order to identify the transforming growth factor beta signaling pathway for the generation of Tfh cells and humoral responses during respiratory viral infections.
  • ProLong Gold antifade reagent was used for immunofluorescence, in order to identify the transforming growth factor beta signaling pathway for the generation of Tfh cells and humoral responses during respiratory viral infections.
  • Lipofectamine 2000 was used for cell transfection, in order to investigate the role of Ca2+ in regulating mobility of TRPV1 channels.
  • DMEM was used for cell culture, in order to investigate the role of Ca2+ in regulating mobility of TRPV1 channels.