P2RX7 Antibody (C-term)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS: 1
- PROTOCOLS
- BACKGROUND
Application ![]()
| IHC-P, WB, E |
---|---|
Primary Accession | Q99572 |
Other Accession | NP_002553.2 |
Reactivity | Human, Mouse |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 68585 Da |
Antigen Region | 563-592 aa |
Gene ID | 5027 |
---|---|
Other Names | P2X purinoceptor 7, P2X7, ATP receptor, P2Z receptor, Purinergic receptor, P2RX7 |
Target/Specificity | This P2RX7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 563-592 amino acids of human P2RX7. |
Dilution | WB~~1:1000 IHC-P~~1:50~100 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | P2RX7 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | P2RX7 |
---|---|
Function | Receptor for ATP that acts as a ligand-gated ion channel. Responsible for ATP-dependent lysis of macrophages through the formation of membrane pores permeable to large molecules. Could function in both fast synaptic transmission and the ATP-mediated lysis of antigen-presenting cells. In the absence of its natural ligand, ATP, functions as a scavenger receptor in the recognition and engulfment of apoptotic cells (PubMed:21821797, PubMed:23303206). |
Cellular Location | Cell membrane; Multi-pass membrane protein |
Tissue Location | Widely expressed with highest levels in brain and immune tissues. |

Provided below are standard protocols that you may find useful for product applications.
Background
P2RX7 belongs to the family of purinoceptors for ATP. This receptor functions as a ligand-gated ion channel and is responsible for ATP-dependent lysis of macrophages through the formation of membrane pores permeable to large molecules. Activation of this nuclear receptor by ATP in the cytoplasm may be a mechanism by which cellular activity can be coupled to changes in gene expression.
References
Kim, M., et al. EMBO J. 20(22):6347-6358(2001)
Gartland, A., et al. J. Bone Miner. Res. 16(5):846-856(2001)
Gu, B.J., et al. J. Biol. Chem. 276(14):11135-11142(2001)
Buell, G.N., et al. Recept. Channels 5(6):347-354(1998)
Rassendren, F., et al. J. Biol. Chem. 272(9):5482-5486(1997)

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