Human P2X2 Purinergic Receptor Cell Line

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  • Concentration-dependent inhibition of P2X2 receptors by pyridoxal-phosphate-6-azophenyl-2',4'-disulfonate (PPADS) and suramin, recorded by FLIPR® intracellular Ca2+ assay. 2′(3′)-O-(4-benzoylbenzoyl)-ATP (Bz-ATP, 3 µM) Ca2+ responses after 30-minute preincubation with the antagonist.
  • Concentration-response relationship for PPADS inhibition of Bz-ATP-induced activation (IC50 value, 0.19 µM). The IC50 value for suramin inhibition was 121 µM (curve not shown). Recording instrument: FLIPR®.

Human P2X2 Purinergic Receptor Cell Line

  • Cat.#:
  • CT6187

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Quick Overview

Human P2X2 Purinergic Receptor-expressing, stable replicating cell line.

Background

The human P2RX2 gene encodes P2X2, an ionotropic ATP receptor that functions as an ATP-activated cation channel expressed in the CNS and dorsal root ganglion neurons. P2X2 channels are therapeutic targets in treatment of pain.
General Info
Product Description Human P2X2 Purinergic Receptor-expressing, stable replicating cell line.
Target Type Ion Channel
Product Type Replicating Cell Line
Family Ligand-Gated
Receptor Purinergic
Sub-Type P2X2
Class Ionotropic purinergic receptor
Therapeutic Area pain & inflammation
Related Services Large-scale Cryopreservation
Gene Name P2RX2
Validated Assay/Platform FLIPR®, QPatch HT
References Alexander SPH, et al., 2007. Br J Pharmocol 150 (Suppl. 1): S1 – S168. Guide to Receptors and Channels.
Host cell HEK293
Mycoplasma Status Negative (MycoAlert Kit)
Storage & Packaging
Packaging Cryopreserved cells, 1-2x106 cells
Storage Recommendation liquid nitrogen
Quantity 1-2 million cells
Product Documentation
Specification Sheet  Download PDF Document