Our work speaks for itself.

Take a look at a selection of our recent projects, crafted with care and designed to make an impact.

Effects on the ion-channel TRPV1. Receptor facilitation and inhibition by Agonist or Antagonist, the [EC80]/[IC80] could be determined. Experiments were performed in a TRPV1-expressing cell-line.

Effects on the ion-channel TRPV1. Receptor facilitation and inhibition by Agonist or Antagonist, the [EC80]/[IC80] could be determined. Experiments were performed in a TRPV1-expressing cell-line.

TRPV1 receptor activation by Capsaicin, the receptor activation was measured in the presence of agonist or antagonist on the TRPV1-expressing cell-line.

TRPV1 receptor activation by Capsaicin, the receptor activation was measured in the presence of agonist or antagonist on the TRPV1-expressing cell-line.

A laser was used to generate a local pulse of heat to activate the heat-sensitive TRPV1 ion channel in an adherent cell culture. Combined with a microfluidic pipette, designed to rapidly switch between several drug treatments in a confined set of cel

A laser was used to generate a local pulse of heat to activate the heat-sensitive TRPV1 ion channel in an adherent cell culture. Combined with a microfluidic pipette, designed to rapidly switch between several drug treatments in a confined set of cells allowed for determining ligands as well as heat activation of this ion channel.

Summary of inhibiting effects from commercial antagonists of TRPV1

Summary of inhibiting effects from commercial antagonists of TRPV1

In-house developed method for investigating memory formation in live mouse hippocampus slices. This living brain tissue was subjected to the Glutamatergic agonist NMDA in a 96-well format and the Calcium influx to the neurons were recorded.

In-house developed method for investigating memory formation in live mouse hippocampus slices. This living brain tissue was subjected to the Glutamatergic agonist NMDA in a 96-well format and the Calcium influx to the neurons were recorded.

In-house developed method for investigating memory formation in live mouse hippocampus slices. This living brain tissue was subjected to the Glutamatergic agonist NMDA in a 96-well format and the Calcium influx to the neurons were recorded.

In-house developed method for investigating memory formation in live mouse hippocampus slices. This living brain tissue was subjected to the Glutamatergic agonist NMDA in a 96-well format and the Calcium influx to the neurons were recorded.

Next

Oncology Projects