Mouse Purinergic Receptor P2X Ligand-Gated Ion Channel 7 (P2RX7) ELISA Kit | P2RX7 elisa kit

Mouse Purinergic Receptor P2X Ligand-Gated Ion Channel 7 (P2RX7) ELISA Kit

Cat. Num. AAA3807516

• Gene Names: P2RX7; P2X7
• Reactivity: Mouse
• Synonyms: Purinergic Receptor P2X Ligand-Gated Ion Channel 7 (P2RX7); Mouse Purinergic Receptor P2X Ligand-Gated Ion Channel 7 (P2RX7) ELISA Kit; P2RX7 elisa kit

• Reactivity: Mouse
• Sequence Length: 595

• Samples: Serum, plasma, cell culture supernate and other biological fluids
• Assay Type: Sandwich
• Detection Range: 100 pg/ml-1600 pg/ml
• Sensitivity: 10 pg/ml

Typical Testing Data/Standard Curve (for reference only)

Related Product Information for P2RX7 elisa kit

Intended Use: The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration ofP2RX7in the sample, This P2RX7ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versusP2RX7concentration. The concentration ofP2RX7in the samples is then determined by comparing the O.D. of the samples to the standard curve.

NCBI and Uniprot Product Information

• NCBI GI #: 119618646
• NCBI GeneID: 5027
• NCBI Official Full Name: purinergic receptor P2X, ligand-gated ion channel, 7, isoform CRA_b
• NCBI Official Synonym Full Names: purinergic receptor P2X 7
• NCBI Official Symbol: P2RX7
• NCBI Official Synonym Symbols: P2X7
• NCBI Protein Information: P2X purinoceptor 7
• Protein Family: P2X purinoceptor

NCBI Description

The product of this gene 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. Multiple alternatively spliced variants have been identified, most of which fit nonsense-mediated decay (NMD) criteria. [provided by RefSeq, Jul 2010]