Anti-P2X5

貨號 Cat. No.
APR-005
規格 Size
50 μl 0.2ml

Description

Anti-P2X5












Product#: APR-005



























Sizes:
50 ml
0.2 ml
 
 
 
 





The P2X5 receptor (P2X5R) belongs to the ligand-gated ion channel P2X family,  

which is activated by extracellular ATP.  



To date, seven receptor subtypes named P2X1-P2X7 have been described.1,2,3  

All P2X subunits, with the exception of P2X6, can assemble to form homomeric or  

heteromeric functional channels.4-5 The P2X5R forms a heteromeric receptor  

with P2X1 receptor. The heteromeric receptor has distinct properties from the P2X1 or P2X5  

homomeric receptors.4,6 The different P2X receptors show distinct expression patterns.  

P2X1-6 have been found in the central and peripheral nervous system, while the P2X7 receptor 

is found in cells of the immune system, particularly antigen presenting cells, and in microglia.  

The P2X5 subunit was first cloned from rat heart, and was reported to be expressed in heart,  

brain, spinal cord and adrenal gland. 



 

Recent papers suggested possible roles for P2X5 receptor in differentiation and apoptosis in keratinocytes  

and ageing rat prostate, respectively.7-10



We are pleased to offer a new antibody to our growing line of ligand-gated ion channel P2X antibodies, 

Anti-P2X5 antibody.












Host:
Rabbit.







 










Epitope:
Peptide (C)RENAIVNVKQSQILHPVKT corresponding to residues 437-455 of  

rat P2X5 (Accession number P51578).








 







 










Putative epitope location:
Intracellular, C-terminus.







 










Homology:
Mouse - 13/18 residues identical.







 










Reactivity Confirmed:
Rat.







 

Applications:










Western Blotting:
.















Western blotting of rat brain membrane:  

1. Anti-P2X5 antibody (1:200). 

2. Anti-P2X5 antibody, 

preincubated with the control peptide antigen.








 

Control antigen included in price









References:














































1.


Prasad, M. et al. (2001) J. Physiol. 573, 667. 


2.


Florenzano, F. et al. (2002) Neuroscience 115, 425.

3.


Ashcroft, F.M. et al. (2000) Ion Channels and Disease Ed.1.

4.


Khakh, B.S. et al. (2001) Pharmacol. Rev. 53, 107. 

5.


Ding, Y. et al. (2000) J. Auton. Nerv. Syst. 81, 289. 

6.


Torres, G.E. et al. (1998) Mol. Pharmacol. 54, 989. 

7.


Greig, A.V. et al. (2003) J. Invest. Dermatol. 121, 1145. 

8.


Greig, A.V. et al. (2003) J. Invest. Dermatol. 120, 1007. 

9.


Slater, M. et al. (2000) Histochem. J. 32, 571. 

10.


Afework, M. and Burnstock, G. (2000) Int. J. Devl. Neuroscience 18, 515. 

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