ENPP2 Antibody

說明書

中文名稱：

ENPP2兔多克隆抗體
貨號：

CSB-PA005573
規格：

￥1090
圖片：
Western Blot analysis of 293 cells using Autotaxin Polyclonal Antibody.
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

Uniprot No.：

Q13822
基因名：

ENPP2
別名：

ATX antibody; ATX X antibody; Autotaxin antibody; Autotaxin t antibody; E NPP 2 antibody; E-NPP 2 antibody; Ectonucleotide pyrophosphatase/phosphodiesterase 2 antibody; Ectonucleotide pyrophosphatase/phosphodiesterase family member 2 antibody; Enpp2 antibody; ENPP2_HUMAN antibody; Extracellular lysophospholipase D antibody; FLJ26803 antibody; LysoPLD antibody; NPP2 antibody; PD IALPHA antibody; PDNP2 antibody; Phosphodiesterase I alpha antibody; Phosphodiesterase I/nucleotide pyrophosphatase 2 antibody; Plasma lysophospholipase D antibody
宿主：

Rabbit
反應種屬：

Human,Mouse,Rat
免疫原：

Synthesized peptide derived from the Internal region of Human Autotaxin.
免疫原種屬：

Homo sapiens (Human)
標記方式：

Non-conjugated
抗體亞型：

IgG
純化方式：

The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
產品提供形式：

Liquid
應用范圍：

WB, ELISA

推薦稀釋比：

Application	Recommended Dilution
WB	1:500-1:2000
ELISA	1:20000

Protocols：

Western Blotting (WB) Protocol
ELISA Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

功能：

Hydrolyzes lysophospholipids to produce the signaling molecule lysophosphatidic acid (LPA) in extracellular fluids. Major substrate is lysophosphatidylcholine. Also can act on sphingosylphosphorylcholine producing sphingosine-1-phosphate, a modulator of cell motility. Can hydrolyze, in vitro, bis-pNPP, to some extent pNP-TMP, and barely ATP. Involved in several motility-related processes such as angiogenesis and neurite outgrowth. Acts as an angiogenic factor by stimulating migration of smooth muscle cells and microtubule formation. Stimulates migration of melanoma cells, probably via a pertussis toxin-sensitive G protein. May have a role in induction of parturition. Possible involvement in cell proliferation and adipose tissue development (Probable). Tumor cell motility-stimulating factor. Required for LPA production in activated platelets, cleaves the sn-1 lysophospholipids to generate sn-1 lysophosphatidic acids containing predominantly 18:2 and 20:4 fatty acids. Shows a preference for the sn-1 to the sn-2 isomer of 1-O-alkyl-sn-glycero-3-phosphocholine (lyso-PAF).
基因功能參考文獻：
1. These results suggest functional interactions among ATX, VEGFR-2, and VEGFR-3 in the modulation of hemovascular and lymphovascular cell activation during vascular development. PMID: 30456868
2. LPAR mRNA and ATX protein levels are anatomic site-dependent in high-grade serous carcinoma and the former are informative of disease outcome. PMID: 30032361
3. Study revealed that serum total ATX and ATX isoforms were significantly associated with the clinical stages of female subjects with melanoma. PMID: 29500864
4. Serum ATX levels may at least partially reflect histological severity in non-alcoholic fatty liver disease. PMID: 29568204
5. ATX-LPA axis facilitates estrogen-induced endometrial cancer cell proliferation via MAPK/ERK signaling pathway. PMID: 29328374
6. Significant suppression of these aforementioned changes was observed after ATX/LPA-receptor/ROCK inhibition as well as suppression of fibrotic changes and MLC and cofilin phosphorylation in HTM cells. PMID: 29305605
7. Autotaxin levels were significantly higher in early-onset preeclampsia group compared with late-onset preeclampsia group. Autotaxin levels were found to be significantly higher in preeclamptic patients compared with control group. Serum autotaxin levels showed a significant positive correlation with maternal systolic, diastolic blood pressures and uric acid levels. PMID: 29058512
8. Results demonstrated, for the first time, that increased serum ATX activity and protein levels are associated with several aspects of quality of life in cholestatic patients as well as with markers of cholestatic liver injury and higher risks of death and transplantation. The study provides novel clinical evidence of the pruritogenic role of the ATX/lysophosphatidic acid axis in the pathogenesis of cholestatic itch. PMID: 27506882
9. ENPP2 silencing increased HBV replication approximately 2.3-fold by enhancing, via the type I IFN signaling pathway, HBV cccDNA (covalently closed circular DNA) translation into viral RNA. PMID: 29414802
10. This study demonstrated that Autotaxin is Related to Metabolic Dysfunction and Predicts Alzheimer's Disease Outcomes. PMID: 27911319
11. Structural and functional studies have revealed what makes ATX a unique lysoPLD, and how secreted ATX binds to its target cells. The ATX catalytic domain shows a characteristic bimetallic active site followed by a shallow binding groove that can accommodate nucleotides as well as the glycerol moiety of lysophospholipids, and by a deep lipid-binding pocket. PMID: 24548887
12. We conclude that an ATM-ATX axis interconnects double-strand breaks with silica-induced inflammation and propagates these effects in epithelial cells PMID: 28968864
13. we present a new crystal structure of ATX in complex with orthovanadate (ATX-VO5), which binds the Ogamma nucleophile of Thr209 and adopts a trigonal bipyramidal conformation, following the nucleophile attack onto the substrate.We propose that ATX follows the associative two-step in-line displacement mechanism. PMID: 27268273
14. The effects of gamma radiation on mRNA levels of autotaxin and 14 inflammatory mediators in adipose tissue and the consequences for radiation therapy and chemotherapy are discussed. PMID: 28539367
15. These findings suggest that the promoter hypomethylation and overexpression of ATX might play a contributory role in the pathogenesis of liver fibrosis in biliary atresia. PMID: 28052132
16. LPA2 mRNA levels were associated with poorer differentiation, and higher LPA6 levels were associated with microvascular invasion in HCC; both became a risk factor for recurrence after surgical treatment when combined with increased serum ATX levels PMID: 27583415
17. AKT signaling played a role in ATX secretion regulation to facilitate ATX ER export by enhancing the nuclear factor of activated T cell-mediated p23 (Sec24C) expression PMID: 28298439
18. Expression of both ATX and IL-6 was increased in systemic scleroderma (SSc) skin, and lysophosphatidic acid-induced IL-6 levels and IL-6-induced ATX levels were increased in fibroblasts from SSc patients compared with controls. PMID: 27390295
19. Elevated levels of autotaxin and soluble markers of immune activation during HCV infection. PMID: 27540113
20. These results suggest that the post-transcriptional regulation of ATX expression by HuR and AUF1 modulates cancer cell migration. PMID: 27784781
21. ATX is highly expressed in renal cell carcinoma and bladder carcinoma. PMID: 27757783
22. With a deeper understanding of the critical role of the autotaxin/lysophosphatidate axis in pancreatic cancer, targeting autotaxin or lysophosphatidate receptor may be a potential and promising strategy for cancer therapy. PMID: 28347252
23. Plasma ATX activity is strongly associated with pruritus in primary biliary cholangitis, authors review the biochemistry of ATX and the rationale for its role in pruritus. [Review] PMID: 27019050
24. Data suggest serum ATX levels correlate with presence/intensity of pruritus in pediatric cholestatic disorders; despite therapy, ATX is up-regulated in children with severe pruritus due to cholestatic disorders (AGS, Alagille syndrome; BA, biliary atresia; progressive familial intrahepatic cholestasis) compared to children with cholestatic disorders without pruritus (BASD, bile acid synthesis defects). [PILOT PROJECT] PMID: 26628447
25. These findings support our previous work showing reduced ATX antigen levels in the peripheral blood of pre-eclamptic women. A disturbance in placental ATX production may be linked to poor placental development and systemic maternal symptoms in early-onset pre-eclampsia. PMID: 26111716
26. These results suggest that autotaxin-LPA-LPA receptor 1-AKT1 signaling axis is critical for maintaining Cancer stem cells(CSC) characteristics through an autocrine loop and provide a novel therapeutic target for ovarian CSCs. PMID: 26800320
27. autotaxin (ATX), is an ecto-lysophospholipase D encoded by the human ENNP2 gene PMID: 25977291
28. Altered expression of ENPP2 is associated with various diseases, such as, inflammation, cancer, fibrosis, rheumatoid arthritis and neural tube defects. (Review) PMID: 26391552
29. Serum ATX correlates with and predicts measures of glucose homeostasis and insulin sensitivity in older humans, suggesting that it may be a potential pathogenic factor and/or diagnostic/therapeutic target for insulin resistance in this population PMID: 26727116
30. ATX was induced in monocytic THP-1 cells by TLR4 ligand lipopolysaccharide (LPS), TLR9 ligand CpG oligonucleotide, and TLR3 ligand poly(I:C), respectively PMID: 26313906
31. Autotaxin is an inflammatory mediator and therapeutic target in thyroid cancer PMID: 26037280
32. The results are discussed in terms of ATX regulation in wound healing and cancer.We, therefore, demonstrate the concept that accumulation of LPA in the circulation decreases ATX production PMID: 25896349
33. Increased serum autotaxin activity represents a highly sensitive, specific and robust diagnostic marker of Intrahepatic cholestasis of pregnancy , distinguishing ICP from other pruritic disorders of pregnancy and pregnancy-related liver diseases. PMID: 25450205
34. blocking tumor-driven inflammation by ATX inhibition is effective in decreasing tumor growth in breast cancers where the cancer cells express negligible ATX. PMID: 26071407
35. Autotaxin is transported in the aortic valve by lipoprotein(a) and is also secreted by valve interstitial cells. PMID: 26224810
36. Data suggest a role for the autotaxin-lysophosphatidic acid axis in toluene diisocyanate toxicity. PMID: 26072274
37. Elevated serum autotaxin was correlated with hepatic dysfunction in biliary atresia. PMID: 25536867
38. In humans, ENPP2 expression in subcutaneous fat and ENPP2 levels in serum were reduced in obese subjects. PMID: 24969110
39. Exogenous ATX controls breast cancer cell proliferation, invasion, and endothelial cell transmigration via interaction tumor integrin alphaVbeta3. PMID: 25277122
40. increase in serum ATX levels in HCC patients may not be caused by abundant ATX production in HCC tissues but by fibrosis in the background livers PMID: 24642343
41. The circulating level of lysophosphatidic acid in a systemic atopic dermatitis model, with severe scratching was probably because of the increased lysophospholipase D activity of autotaxin (ATX) in the blood rather than in plasma. PMID: 24641902
42. potential biomarker for atopic dermatitis PMID: 24582488
43. high levels of c-Jun enhance motility in part by driving the expression of ENPP2/Autotaxin PMID: 24852265
44. The present review provides an overview of the ATX-LPA signalling axis and collates current knowledge regarding its specific role in breast cancer. PMID: 25195735
45. Data indicate that inhibition of autotaxin (ATX) significantly reduced T cell migration. PMID: 24935929
46. autotaxin-mediated disease processes PMID: 24560789
47. The results of this study showed that ATX activity was significantly higher (p value<0.0001) in MS patients than those patients diagnosed with neurological disease. PMID: 24984830
48. ATX expression is up-regulated in obese patients and mice in relationship with insulin resistance and impaired glucose tolerance. [Review] PMID: 23639740
49. Endothelial ATX acts through lysophosphatidic acid signaling to promote renal tumorigenesis and is functionally involved in the acquired resistance to sunitinib. PMID: 24122794
50. Downregulation of human ATX inhibits the growth of human gastric cancer xenografts in nude mice. PMID: 23258351
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亞細胞定位：

Secreted.
蛋白家族：

Nucleotide pyrophosphatase/phosphodiesterase family
組織特異性：

Detected in blood plasma (at protein level). Predominantly expressed in brain, placenta, ovary, and small intestine. Expressed in a number of carcinomas such as hepatocellular and prostate carcinoma, neuroblastoma and non-small-cell lung cancer. Expressed
數據庫鏈接：

HGNC: 3357

OMIM: 601060

KEGG: hsa:5168

UniGene: Hs.190977

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