P2RX7 Antibody, Biotin conjugated
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中文名稱:P2RX7兔多克隆抗體, Biotin偶聯(lián)
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貨號:CSB-PA859103LD01HU
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規(guī)格:¥880
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其他:
產(chǎn)品詳情
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產(chǎn)品名稱:Rabbit anti-Homo sapiens (Human) P2RX7 Polyclonal antibody
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Uniprot No.:
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基因名:
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別名:ATP receptor antibody; P2rx7 antibody; P2RX7_HUMAN antibody; P2X purinoceptor 7 antibody; P2X7 antibody; P2Z receptor antibody; Purinergic receptor antibody; purinergic receptor P2X, ligand gated ion channel, 7 antibody
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宿主:Rabbit
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反應種屬:Human
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免疫原:Recombinant Human P2X purinoceptor 7 protein (110-247AA)
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免疫原種屬:Homo sapiens (Human)
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標記方式:Biotin
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克隆類型:Polyclonal
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抗體亞型:IgG
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純化方式:>95%, Protein G purified
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濃度:It differs from different batches. Please contact us to confirm it.
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保存緩沖液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
產(chǎn)品提供形式:Liquid
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應用范圍:ELISA
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Protocols:
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儲存條件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相關產(chǎn)品
靶點詳情
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功能: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.
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基因功能參考文獻:
- Results suggest the pathophysiological role of purinergic receptor P2X7 (P2X7) in pancreatic disease and recovery. PMID: 29683976
- The P2x7 ion channel receptor was regularly absent in both the periodontal ligament and dental tissues PMID: 29289709
- These results suggest that ERK pathway is involved in the proliferation and migration of glioma cells induced by P2X7R activation. PMID: 29546069
- Increased P2X7 receptor expression in monocytes are manifestations of chronic inflammation in the early stages of chronic kidney disease. PMID: 29375053
- the P2X7R rs3751143 and ER-alpha PvuII two-locus interaction confers a significantly high susceptibility to osteoporosis in Chinese postmenopausal women. PMID: 28884379
- that the P2X7R rs3751143 functional polymorphism might contribute to osteoporosis susceptibility in Chinese postmenopausal women PMID: 28497417
- indicating the involvement of P2X7R in the growth of esophageal squamous cell carcinoma PMID: 28397110
- Data show that Pr2x7 gene deletion protects from HFD-induced NASH, possibly through blunted activation of NLRP3 inflammasome. PMID: 29270247
- this study demonstrates that P2X7 is not essential for development of imiquimod -induced psoriasis-like inflammation PMID: 28597172
- This study revealed that the P2X7R/NLRP3 pathway plays important roles in IL-1beta secretion and inhibition of Toxoplasma gondii proliferation in small intestinal epithelial cells. PMID: 29291748
- P2X7R contributes to the progression of spinal TB. The P2X7 -762C>T and 489C>T polymorphisms are correlated with susceptibility to spinal TB. Carrying the -762CC genotype and 489T allele increases the risk of developing spinal TB in a Southern Chinese Han population. PMID: 29158203
- Increased expression of P2X7R in peripheral blood mononuclear cells from patients with rheumatoid arthritis.P2X7R role in th17 cells differentiation. PMID: 27775097
- results show that P2X7 is a scavenger receptor with important function in the CNS but its phagocytic function has features distinct from its pore function. Both P2X7 pore formation and P2X7-mediated phagocytosis should be considered in the design of new P2X7 antagonists for the treatment of CNS diseases. PMID: 29329985
- This pathway provides new insight into factors that increase dynamic blebbing and identifies new targets, such as P2X7, that can be used to improve the culture of cells with therapeutic potential. PMID: 28672157
- a major role for P2X7R and P2Y11R in ATP-mediated inhibition of tumor-derived endothelial cell migration, is reported. PMID: 27586846
- To investigate the correlation between P2X7R, NLRP3 and cell growth, NLRP3 was silenced in THP-1 cells, a leukemic cell line that natively expresses both NLRP3 and P2X7R. NLRP3 silencing enhanced P2X7R expression and promoted growth. On the contrary, NLRP3 overexpression caused accelerated apoptosis. PMID: 27221966
- Genetic polymorphisms of the P2X7 gene associated with susceptibility to and prognosis of pulmonary tuberculosis. PMID: 28495473
- The results suggest that although the 1068 G>A polymorphism of the P2RX7 gene is associated with an increased beta-cell function and IL-1Ra release in type 2 diabetes patients, the glycemic control is not significantly affected by the presence of this SNP. PMID: 29425823
- These data suggest that P2X7R activation may contribute to the high prevalence of kidney disease found in diabetics. PMID: 28434946
- In conclusion, the results suggest that P2X7R may promote IL-6, IL-8 and MCP-1 production and secretion and contribute to the invasion and adhesion of craniopharyngiomas to the surrounding tissue. PMID: 28389503
- P2X7R is expressed by three malignant pleural mesothelioma cell lines established from MPM patients but not by mesothelial cells from healthy subjects PMID: 27391069
- A total of 163 patients and 201 health controls were enrolled in this study and polymorphisms of NLPR1, NLRP3, and P2X7R genes were detected by PCR..Our study demonstrated the potentially significant role of NLRP1 rs878329 (G>C) in developing susceptibility to the partial seizures in a Chinese Han population. PMID: 28503575
- Inheritance of the C/C genotype at position 253 in the P2RX7 gene may contribute to the risk of HPV-16 associated cervical squamous cell carcinoma in Taiwanese women. PMID: 27779103
- This study demonstrated that ischemic preconditioning Induces Long-Lasting Increase in P2X7 Receptor in Astrocytes. PMID: 28063215
- The link is being discussed between P2X7R signaling and TG2 export, a pathway that has been recently discovered and tied extracellular protein modifications into the danger signal-mediated innate immune response. (Review) PMID: 27562793
- P2X7R is involved in propagation of mechanically-induced intercellular signaling in addition to the known mechanisms involving calcium signaling via P2Y2 receptors and gap junction. PMID: 27856358
- this study shows that P2X7R is directly involved in the modulation of the antiviral and inflammatory process that occurs during Dengue virus infection in vitro PMID: 26969484
- These results suggest that mechanical stimuli activate P2X7 might induce ECMPs expression through PYK2 except in the case of OPN expression. Altogether, mechanical stimuli-induced ECMPs production might be implicated by extracellular ATP secretion or integrin via PYK2 activation. PMID: 29061307
- The results indicate that P2X7 receptors may play a significant role in contributing to the unwanted activation of mast cells in chronic inflammatory conditions where extracellular ATP levels are elevated PMID: 26910735
- In vitro and in vivo results provide support for the involvement of an oxidative stress through P2X7 receptor activation and mitochondrial dysfunction in the pathophysiology of oxaliplatin-induced neuronal injury and likely to painful neuropathy. PMID: 23826152
- Eight Single nucleotide polymorphisms loci, including rs1653624, rs10160951, rs1718119, rs7958316, rs16950860, rs208294, rs17525809 and rs2230912, were screened and detected, and rs1653624, rs7958316 and rs17525809 were associated with gout arthritis. P2X7R function associated single nucleotide polymorphisms may be related to gouty arthritis. PMID: 28797095
- The loss-of-function SNP rs2230911 in P2X7, that negatively affect NLRP3-inflammasome activation, confers susceptibility toward active pulmonary tuberculosis in Brazilian Amazon cohort. PMID: 27101784
- this review discusses P2X7R structure and its contribution to inflammation and host defense PMID: 28723547
- P2X7R expression was correlated with enhanced tumor grade and metastasis in colorectal carcinoma patients. PMID: 28412208
- Our present study shows that loss of function of the P2X7 receptor in mice induces retinal changes representing characteristics of early age-related macular degeneration. PMID: 28628761
- Single nucleotide polymorphism in P2X7R gene is associated with pulmonary non-tuberculous mycobacterial disease. PMID: 28233049
- Our results reveal that P2RX7 rs2230911 may be associated with primary gout risk in a Chinese Han male population and allele G may be a susceptibility factor for primary gout. PMID: 28243797
- We think that the unbiased reader will follow our argumentation on astrocytic or microglial P2X7Rs being the primary targets of pathologically high extracellular ATP concentrations, although a neuronal localization of these receptors cannot be fully excluded either. [review] PMID: 28747388
- Together, this body of research suggests that P2X7R may constitute an important therapeutic target for a variety of neurological disorders. PMID: 28747389
- In addition, purinergic receptor P2X, ligand-gated ion channel 7 (P2X7) was downregulated in CD36-knockdown 3T3-L1 cells, suggesting that the suppression of CD36 attenuates adipogenesis via the P2X7 pathway in 3T3-L1 cells. PMID: 28712872
- analysis of the M1/M2 functional imprinting of primary microglia and the role played by P2X7 and miR-125b in amyotrophic lateral sclerosis microglia activation [review] PMID: 28090150
- Study observed a downregulation of purinergic P2X7 receptors in peripheral blood mononuclear cells of amyotrophic lateral sclerosis (ALS) patients compared to controls. PMID: 27453058
- Data suggest that specific serine residues in purinergic receptors play key roles in both agonist binding and receptor sensitization/desensitization: in rat P2rx7, point mutation F288S (phenylalanine 288 > serine) results in a slower rate of ATP binding/unbinding and stabilization of non-sensitized receptor states; in human P2RX7, Y288F (but not Y288S) results in a "rat-like" receptor with a fast deactivation rate. PMID: 28616989
- This study showed that the ATP-gated P2X7 receptor is upregulated in experimental epilepsy and resected hippocampus from epilepsy patients. PMID: 27251615
- ATP release by Muller cells and P2X7 upregulation in RECs. These findings are likely of in vivo relevance since CD40 upregulates P2X7 in RECs in diabetic mice and CD40 is known to be required for retinal capillary degeneration. PMID: 27893093
- Our study revealed a significant association between three P2X7R gene polymorphisms and pulmonary tuberculosis in a Tibetan Chinese population. PMID: 27672203
- circadian oscillations of intracellular calcium depend on the activation of purinergic P2X7 receptors PMID: 28139817
- the biochemical and molecular knowledge of P2X7R in IFCD is useful to shed further light about the participation of purinergic system in the pathogenesis of CD, and consequently, may help to avoid the progression of disease. PMID: 28062289
- The P2X7R rs3751142 genetic variants was not implicated in the development of gout in the male Korean population. However, we found that in a pair-wise comparison of the CA/TT P2X7R and CARD8 genotype combination was shown to have an increased trend for the risk of gout. PMID: 27550484
- Five gene polymorphisms, -762C>T (rs2393799), 946G>A (rs28360457), 1513A>C (rs3751143), 1068G>A (rs1718119), and 1096C>G (rs2230911), were selected. Our results suggest that 3 of the 5 polymorphisms of P2RX7 described above (1513A>C, 946G>A, and 1068G>A) are significantly associated with Hepatocellular Carcinoma susceptibility in a Chinese Han population. PMID: 27272229
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亞細胞定位:Cell membrane; Multi-pass membrane protein.
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蛋白家族:P2X receptor family
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組織特異性:Widely expressed with highest levels in brain and immune tissues.
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