WNT7A Antibody, HRP conjugated

說明書

中文名稱：

WNT7A兔多克隆抗體, HRP偶聯
貨號：

CSB-PA026141LB01HU
規格：

￥880
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) WNT7A Polyclonal antibody
Uniprot No.：

O00755
基因名：

WNT7A
別名：

Protein Wnt-7a antibody; Protein Wnt-7a precursor antibody; Proto oncogene Wnt7a protein antibody; proto-oncogene wnt7a protein antibody; wingless-type MMTV integration site family; member 7A antibody; Wnt family member 7A antibody; WNT7A antibody; WNT7A_HUMAN antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Protein Wnt-7a protein (126-302AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

HRP
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

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

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
產品提供形式：

Liquid
應用范圍：

ELISA
Protocols：

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：

Ligand for members of the frizzled family of seven transmembrane receptors that functions in the canonical Wnt/beta-catenin signaling pathway. Plays an important role in embryonic development, including dorsal versus ventral patterning during limb development, skeleton development and urogenital tract development. Required for central nervous system (CNS) angiogenesis and blood-brain barrier regulation. Required for normal, sexually dimorphic development of the Mullerian ducts, and for normal fertility in both sexes. Required for normal neural stem cell proliferation in the hippocampus dentate gyrus. Required for normal progress through the cell cycle in neural progenitor cells, for self-renewal of neural stem cells, and for normal neuronal differentiation and maturation. Promotes formation of synapses via its interaction with FZD5.
基因功能參考文獻：
1. These results indicate that Wnt7a signaling inhibits inflammatory stimuli-induced catabolic gene expression in human articular chondrocytes and is sufficient to attenuate MMP activities and promote joint cartilage integrity in mouse experimental OA, demonstrating a novel effect of Wnt7a on regulating OA pathogenesis. PMID: 28165497
2. Wnt7a induces a unique phenotype of monocyte-derived macrophages with lower phagocytic capacity and differential expression of pro- and anti-inflammatory cytokines PMID: 28872671
3. This report deals with linkage studies and exome sequencing, disclosing a novel variant in WNT7A, c.934G>A (p.Gly312Ser), as the cause of this Santos syndrome. PMID: 28855715
4. A homozygous novel WNT7A mutation was identified in a child with Al-Awadi-Raas-Rothschild syndrome accompanied by dental abnormalities and his parents with dental abnormalities. PMID: 28917830
5. Activation of the WNT/CTNBB1 pathway via WNT7A might play a role in PTC development. PMID: 28456695
6. Results show that Wnt7a expression is significantly upregulated in epithelial cells of ovarian cancer which correlates with STAT4 expression and provide evidence that STAT4 promotes ovarian cancer metastasis via tumor-derived Wnt7a-induced activation of cancer-associated fibroblasts. PMID: 28114283
7. WNT7A is a direct target of miR-15b in ovarian cancer cell line. PMID: 27195958
8. The findings presented in this fetus are compatible with diagnosis of Al-Awadi-Raas-Rothschild syndrome , expanding the mutational spectrum of limb malformations arising from defects in WNT7A PMID: 27638328
9. Wnt7a is involved in the transformation of the retinal pigment epithelium. PMID: 26388562
10. Wnt7a overexpression is associated with an unfavorable prognosis and that positive Wnt7a may be an independent prognosis factor influencing OS and DFS prediction in colorectal cancer patients. PMID: 26055144
11. identified Iloprost, a prostacyclin analog, which initiates downstream signaling cascades similar to that of Wnt7a, as a novel inducer of cellular senescence, presenting potential future clinical translational strategies PMID: 25728679
12. Prognosis was significantly more favorable for patients with high Wnt7A expression. PMID: 25632963
13. loss of the Wnt7a gene induced by promoter methylation might be a prognostic factor for non-small cell lung carcinoma PMID: 25653486
14. this is the first study reporting reduced WNT7A levels in cervical cancer -derived cells and that ectopic WNT7A restoration negatively affects cell proliferation and migration. PMID: 25978974
15. Wnt7a has a role in specifying the fate of neural crest-like cells via suppression of notch in the human skin microenvironment PMID: 25705850
16. findings suggest a central role of the WNT7A-PAX6 axis in corneal epithelial cell fate determination, and point to a new strategy for treating corneal surface diseases PMID: 25030175
17. Binding of Wnt7a to Fzd7 leads to an activation of noncanonical Wnt signaling, resulting in directed myogenic stem cell migration and enhanced engraftment. PMID: 24711502
18. Novel mutations in the WNT7A gene in two unrelated cases of Al-Awadi Raas-Rothschild syndrome. PMID: 23727605
19. Gene expression profiling identifies WNT7A as a key SVZ-glial factor lacking in OB-glia that enhances self-renewal, thereby improving the propagation of OB-NSC cultures. PMID: 22987443
20. Overexpression of Wnt7a may contribute to the progression of endometrial cancer and thus may serve as a new biomarker to predict the prognosis of endometrial cancer. PMID: 23321718
21. WNT7A gene is inactivated by genetic/epigenetic alterations in clear cell RCC and demonstrates tumor suppressor properties PMID: 23056560
22. Wnt7a is lost by methylation in a subset of tumors and that this methylation is maintained by DNMT1 PMID: 22403725
23. Reexpression of WNT7A during malignant transformation of ovarian epithelial cells plays a critical role in ovarian cancer progression mediated by WNT/beta-catenin signaling pathway. PMID: 22232518
24. Wnt7a has a role in postmenstrual regeneration and proliferation of endometrial glands and luminal epithelium in primates PMID: 22294752
25. Mutations in the coding sequence of WNT7A are not responsible for mullerian duct abnormalities in the Chinese population. PMID: 22177312
26. The novel missense homozygous mutation (p.Gly204Ser) in the WNT7A gene is a unique mutation in the degree of loss of function in the upper limb development which ranges from mild to complete absence of both upper limbs (amelia). PMID: 21344627
27. Partial loss of WNT7A function resulted in Fuhrmann syndrome, while complete loss of WNT7A function resulted in the more severe phenotype of Al-Awadi-Raas-Rothschild syndrome. PMID: 21271649
28. Abnormalities in the Wnt7a pathway (located in the dorsal ectoderm) produce several clinically relevant conditions. PMID: 20709709
29. A novel homozygous missense mutation in coding exon 4 of the WNT7A was detected in both affected daughters (c.664C > T) leading to an amino acid exchange from arginine to tryptophan (p.Arg222Trp; R222W). PMID: 20949531
30. The activity of the Sprouty4 promoter is increased by Wnt7A/Frizzled 9 homolog (Fzd9) signaling through peroxisome proliferator-activated receptor gamma in lung cancer cells. PMID: 20501643
31. High Wnt7a expression in ovarian cancer may be associated with poor prognosis. PMID: 20845993
32. Expression levels of Wnt7A, beta-catenin, and FoxA1, along with cell-type specific markers, are observed to vary with differentiation and often also in response to the presence of heparin during the time of exposure to heparin. PMID: 20503388
33. Results suggest that this diminished expression of the WNT7A gene may be related to a supposed protection of fragile X syndrome patients to develop cancer. PMID: 20470940
34. Female mammals with a deficiency in the product of Wnt7a gene are infertile as a result of abnormal development of the uterus and the oviducts. PMID: 19849868
35. WNT7a gene expression is regulated by TGF-beta1 through the intracellular beta-catenin-TCF pathway PMID: 12893825
36. provides support that E-cadherin induction by WNT/beta-catenin signaling is an evolutionarily conserved pathway operative in lung cancer cells and that loss of expression may be important in lung cancer development or progression PMID: 12937339
37. WNT7A mutations are an unlikely cause of Mullerian duct derivative abnormalities in humans PMID: 14550385
38. Wnt-7a is associated with cartilage destruction by regulating the maintenance of differentiation status and the apoptosis of articular chondrocytes via different mechanisms PMID: 15082716
39. analysis of multiple Wnt mRNAs in non-small cell lung cancer (NSCLC) cell lines and primary lung tumors revealed markedly decreased Wnt-7a expression compared with normal short-term bronchial epithelial cell lines and normal uninvolved lung tissue PMID: 15705594
40. By regulating the proliferation of corneal epithelial cells, Wnt-7a and MMP-12 appear to contribute to corneal wound healing PMID: 15802269
41. Partial loss of WNT7A causes Fuhrmann syndrome, whereas the more severe limb truncation phenotypes observed in Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome result from null mutations. PMID: 16826533
42. ERK5-dependent activation of PPARgamma represents a major effector pathway mediating the anti-tumorigenic effects of Wnt 7a and Fzd 9 in non-small cell lung cancer cells PMID: 16835228
43. the absence of tumour-specific somatic events in WNT7A and HDAC11 suggests that these genes are unlikely to have a classical tumour suppressor gene role in sporadic malignant pancreatic endocrine tumours PMID: 17201809
44. WNT7A plays a role in the pathophysiology of endometriosis. PMID: 17588571
45. These biological tools could help lead to a better understanding of Wnt-Fzd interactions and the identification of new modulators of Wnt signaling. PMID: 18230341
46. WNT7A gene is unlikely to be a major contributor to the aetiology of familial congenital talipes equinovarus PMID: 18538017
47. Based on these results it is unlikely CAND2 and WNT7a are the major genes that causes clubfoot. PMID: 19159115
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相關疾病：

Limb pelvis hypoplasia aplasia syndrome (LPHAS); Fuhrmann syndrome (FUHRS)
亞細胞定位：

Secreted, extracellular space, extracellular matrix. Secreted.
蛋白家族：

Wnt family
組織特異性：

Expression is restricted to placenta, kidney, testis, uterus, fetal lung, and fetal and adult brain.
數據庫鏈接：

HGNC: 12786

OMIM: 228930

KEGG: hsa:7476

STRING: 9606.ENSP00000285018

UniGene: Hs.72290

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