Taconic's portfolio of ADME-Tox models and services
| Taconic Transgenic Models™ | Traditional Animal Models | Surgically Modified Models | Contract Research Solutions |
|---|---|---|---|
| Bcrp Mouse | Sprague Dawley® Rat | Jugular Vein Cannulation | Compound Administration |
| Mdr1a Mouse | Wistar Hannover GALAS™ Rat | Carotid Artery Cannulation | Interim blood sampling |
| Mdr1a/b Mouse | ICR mouse | Femoral Artery Cannulation | Clinical observation |
| Mdr1a/b-Bcrp Mouse | Black 6 Mouse | Femoral Vein Cannulation | Terminal blood collection |
| HRN™ Mouse | NMRI Mouse | Portal Vein Cannulation | Tissue harvesting |
| Mrp1 Mouse |   | Bile Duct with Duodenal Return |   |
| Mrp2 Mouse |   | Telemetry Implants |   |
| Oct1/2 Mouse |   |   |   |
| Pparα Mouse |   |   |   |
| PXR Mouse |   |   |   |
HRN™ Mouse: The Hepatic Reductase Null Mouse, developed by CXR Biosciences, is a conditional knockout of Por, resulting in a mouse that lacks cytochrome P450 activity in the liver. The HRN™ mouse is useful for determining the role of hepatic P450 metabolism in drug disposition. It can provide information on whether parent or metabolite compounds are responsible for observed efficacy or toxicity. This model allows the study of in vivo efficacy using smaller amounts of compound.
PXR Mouse: Pregnane X Receptor (PXR) is a member of the nuclear receptor family of ligand-activated transcription factors that has evolved to protect the body from toxic chemicals. This receptor is activated by a structurally diverse collection of xenobiotics, including several widely-used prescription drugs. PXR stimulates the transcription of multiple genes involved in the detoxification and elimination of these potentially harmful chemicals. This model carries a homozygous disruption of PXR and may be used to study the role of PXR in drug metabolism and excretion.
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