HUMAN RECOMBINANT NK1 RECEPTOR

MULTISCREEN™ DIVISION-ARRESTED CELL LINE

Product Information

Catalog Number:
DC1303 

Lot Number:
DC1303-021122 

Quantity:
1 vial (4 x 106) frozen cells

Freeze Medium:
Cellbanker 2 (Amsbio)

Host cell:
HEK293T

Transfection:
Expression vector containing full-length human TACR1 cDNA (GenBank Accession Number NM_001058.2) with FLAG tag sequence at N-terminus 

Recommended Storage:
Liquid nitrogen upon receiving

Propagation Medium: DMEM, 10% FBS

Data Sheet

Background: NK1 (or tachykinin receptor TACR1) is a selective receptor for substance P with relatively higher affinity for neurokinin A compared to neurokinin B (100- and 500-fold lower). Neurons in lamina I of the spinal dorsal horn express the NK1 receptor for substance P and mediate hyperalgesia, an enhanced sensitivity to painful stimuli. Although substance P does not mediate the signaling of acute pain or hyperalgesia, it is essential for the full development of stress-induced analgesia and for an aggressive response to territorial challenge. It is also suggested that substance P is important for orchestrating the response of the animal to major stressors such as pain, injury or invasion of territory. Modulation of substance P activity offers a radical new approach to the management of depression, anxiety and stress. The substance P receptor is highly expressed in areas of the brain that are implicated in these behaviors. 

Application: Functional assays

Figure 1. Dose-dependent calcium flux upon treatment with ligand, measured with MULTISCREEN™ Calcium 1.0 No Wash Assay Kit (Multispan MSCA01). 

References:

Lecci et al. (2000) Peripheral actions of tachykinins. Neuropeptides 34:303-313. 

Quartara and Maggi (1997) The tachykinin NK1 receptor. Part I: ligands and mechanisms of cellular activation. Neuropeptides 31:537-563. 

Quartara and Maggi (1998) The tachykinin NK1 receptor. Part II: distribution and pathophysiological roles. Neuropeptides 32:1-49.

FOR RESEARCH USE ONLY.
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