NGFR Antibody, HRP conjugated

說明書

中文名稱：

NGFR兔多克隆抗體, HRP偶聯
貨號：

CSB-PA10479B0Rb
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) NGFR Polyclonal antibody
Uniprot No.：

P08138
基因名：

NGFR
別名：

CD271 antibody; CD271 antigen antibody; Gp80 LNGFR antibody; Gp80-LNGFR antibody; Low affinity nerve growth factor receptor antibody; Low affinity neurotrophin receptor p75NTR antibody; Low-affinity nerve growth factor receptor antibody; Nerve growth factor receptor antibody; Nerve growth factor receptor TNFR superfamily member 16 antibody; NGF receptor antibody; Ngfr antibody; p75 ICD antibody; p75 Neurotrophin receptor antibody; p75 NTR antibody; p75(NTR) antibody; p75NTR antibody; TNFR Superfamily Member 16 antibody; TNFRSF16 antibody; TNR16_HUMAN antibody; Tumor necrosis factor receptor superfamily member 16 antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Tumor necrosis factor receptor superfamily member 16 protein (277-391AA)
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：

Low affinity receptor which can bind to NGF, BDNF, NTF3, and NTF4. Forms a heterodimeric receptor with SORCS2 that binds the precursor forms of NGF, BDNF and NTF3 with high affinity, and has much lower affinity for mature NGF and BDNF. Plays an important role in differentiation and survival of specific neuronal populations during development. Can mediate cell survival as well as cell death of neural cells. Plays a role in the inactivation of RHOA. Plays a role in the regulation of the translocation of GLUT4 to the cell surface in adipocytes and skeletal muscle cells in response to insulin, probably by regulating RAB31 activity, and thereby contributes to the regulation of insulin-dependent glucose uptake. Necessary for the circadian oscillation of the clock genes ARNTL/BMAL1, PER1, PER2 and NR1D1 in the suprachiasmatic nucleus (SCmgetaN) of the brain and in liver and of the genes involved in glucose and lipid metabolism in the liver.
基因功能參考文獻：
1. results demonstrate that cells with in vitro ASC traits can be obtained from both CD271(+) and CD271(-) stromal populations of human adipose tissue. In addition, gene expression profiling and in situ localization analyses indicate that the CD271(+) population displays a pericytic phenotype. PMID: 29125884
2. loss of epidermal CD271(+) keratinocytes seemed necessary for melanoma development PMID: 29678478
3. Cleaved intracellular domain of CD271 controls proliferation, while the interaction of CD271 with the neurotrophin receptor Trk-A modulates cell adhesiveness through dynamic regulation of a set of cholesterol synthesis genes relevant for patient survival. PMID: 29215016
4. Results show that glioma cells with p75NTR overexpression demonstrated certain unique characteristics of tumor-initiating cells, such as neurosphere formation, high colony proliferation, and resistance to radiotherapy and chemotherapy. PMID: 30194166
5. we found good intra-class correlation in CD271 + MSC score among individual pathologists, with excellent performance by the group as a whole. Prospective studies of CD271 + MSC density are necessary to corroborate its diagnostic and prognostic utility. PMID: 27808583
6. High p75(NTR) expression is associated with esophageal squamous cell carcinoma. PMID: 28534989
7. Collectively, CD271 initiates tumor formation by increasing the cell proliferation capacity through CDKN1C suppression and ERK-signaling activation, and by accelerating the migration signaling pathway in hypopharyngeal cancer. PMID: 27469492
8. Study shows that p75 pan-neurotrophin receptor is upregulated in the nerve fibers and inflammatory cells in the local tissue in inflammatory pain. PMID: 27251195
9. Dermal CD271+ cells are closely associated with wound healing. PMID: 28127619
10. p75NTR+ cells isolated from tongue squamous cell carcinoma (TSCC) cell lines possess the characteristics of cancer stem cells; therefore, p75NTR may be considered a useful surface marker for the identification of TSCC stem cells. PMID: 28447720
11. This study show evidence of variation in plasmatic p75NTR receptor expression during the progression of dementia. PMID: 27802234
12. p75(NTR) was overexpressed in anaplastic thyroid cancers compared with papillary and follicular subtypes PMID: 29037860
13. p75NTR, mainly expressed in tumor tissues, was significantly associated with higher Fuhrman grade in multivariate analysis. these data highlight for the first time an important role for p75NTR in renal cancer and indicate a putative novel target therapy in renal cell carcinoma. PMID: 27120782
14. Here, the authors unveil nerve growth factor receptor (NGFR, p75NTR or CD271) as a novel p53 inactivator. p53 activates NGFR transcription, whereas NGFR inactivates p53 by promoting its MDM2-mediated ubiquitin-dependent proteolysis and by directly binding to its central DNA binding domain and preventing its DNA-binding activity. PMID: 27282385
15. Data suggest that p75NTR as a central regulator of glioma tumorigenesis, the tumor microenvironment, and tumor invasiveness; p75NTR may contribute to the drug resistance of glioma. [REVIEW] PMID: 28215302
16. These results demonstrated that EpCAM + p75NTR+ CTC count was a more accurate diagnostic marker than EpCAM+ CTC count, suggesting the highly metastatic potential of CTCs with p75NTR expression. PMID: 28560678
17. Co-immunoprecipitation and biochemical fractionation data suggested that p75 TM stimulates TrkB phosphorylation at the cell membrane. PMID: 28821608
18. hese results suggest that LNGFR(+)THY-1(+) cells identified following NCLC induction from ESCs/iPSCs shared similar potentials with multipotent MSCs. PMID: 27178356
19. the results indicate that CD271 loss is critical for melanoma progression and metastasis. PMID: 27328305
20. For Fat3, the Kif5-ID is regulated by alternative splicing, and the timecourse of splicing suggests that the distribution of Fat3 may switch between early and later stages of retinal development. In contrast, P75NTR binding to Kif5B is enhanced by tyrosine phosphorylation and thus has the potential to be dynamically regulated on a more rapid time scale PMID: 27788242
21. p75(NTR) and NIX may play critical roles in intracerebral hemorrhage-induced neuronal apoptosis in vitro and in vivo. PMID: 27726026
22. The results of this study suggest that p75(+) hDPSC may denote a subpopulation with greater neurogenic potential in human dental pulp stem cells. PMID: 27469433
23. here for the first time, hsa-miR-939 is introduced as a novel key regulator of NGFR expression and its involvement in cell death/survival processes is suggested. PMID: 28229962
24. The receptors p75 and TrkB are more highly expressed in deep infiltrating endometriosis than in peritoneal tissues. PMID: 27519317
25. e disappearance of the superiority in tumorigenicity in vitro and vivo in CD271+ OS cells. CONCLUSION: The results above demonstrated that autophagy contributes to the stem-like features of CD271+ OS CSCs. Inhibition of autophagy is a promising strategy in the CSCs-targeting OS therapy. PMID: 27863492
26. hA17-29 aggregate toxicity seems to be mediated by RAGE and p75-NGFR receptors PMID: 27804051
27. Results revealed that most of the p75NTR-positive cells were in a mitotically quiescent state, while the majority of the p75NTR-negative cells were actively proliferating in esophageal squamous cell carcinoma. PMID: 26984177
28. Data show that under reducing conditions, p75 neurotrophin receptor transmembrane (TM) domain (p75-TM-WT) is in a monomer-dimer equilibrium with the cysteine (Cys 257) residue located on the dimer interface. PMID: 27056327
29. p75NTR and CRABP1 modulate the effect of fenretinide on neuroblastoma cells PMID: 26843908
30. Identify a novel signaling pathway in hepatocytes triggered by ligand-activated p75NTR that via p38 MAPK and caspase-3 mediate the activation of SREBP2. This pathway may regulate LDLRs and lipid uptake particularly after injury or during tissue inflammation accompanied by an increased production of growth factors, including NGF and pro-NGF. PMID: 26984409
31. Studies indicate that neurotrophin receptor p75(NTR) mediates Huntington's disease-associated synaptic and memory dysfunction. PMID: 26700963
32. The percentage of p75NTR+ peripheral blood mononuclear cells increased in early stages of chronic obstructive pulmonary disease (I-II), while TrKA+ peripheral blood mononuclear cells increased in late stages (III-IV). PMID: 26408608
33. High p75NTR expression is associated with esophageal cancer. PMID: 26897248
34. RIP2 and RhoGDI bind to p75(NTR) death domain at partially overlapping epitopes with over 100-fold difference in affinity, revealing the mechanism by which RIP2 recruitment displaces RhoGDI upon ligand binding. PMID: 26646181
35. preventing phosphorylation of p75(NTR) by pharmacological inhibition of PKA, or by a mutational strategy, cripples p75(NTR)-mediated glioma invasion resulting in serine phosphorylation within the C-terminal PDZ-binding motif (SPV) of p75(NTR). PMID: 26119933
36. NGFR Ser205Leu polymorphism modulates the autonomic vagal outflow to the heart, particularly in men. PMID: 26278479
37. Findings show no association of SNPs in NTRK2 and NGFR genes with completed suicide in Slovenian population. PMID: 26462037
38. expression of HIF-1alpha and CD271 in melanomas at different phases of progression, as evaluated by histology and reflectance confocal microscopy PMID: 25739328
39. there are 15 positive studies among 30 studies regarding BDNF/TRKB/P75NTR polymorphisms antidepressant efficacy in depressed patients--{REVIEW} PMID: 26122862
40. The ATF4/p75NTR/IL-8 signal pathway may have an important role in EndoMT induced by SFO. PMID: 24905361
41. Data indicate that p75 neurotrophin receptor p75(NTR) could be a potential therapeutic target for retinal pigment epithelium (RPE) hypoxia or oxidative stress diseases. PMID: 25200140
42. p75(NTR) and alpha9 integrin subunit are not closely associated through their cytoplasmic domains, most probably because of the molecular interference with other cytoplasmic proteins such as paxillin. PMID: 25748048
43. Activation of p75NTR receptor identified that the receptor predominantly assembles as a trimer in brain tissue. PMID: 26311773
44. CD271 expression is associated with stage and lymph node metastasis in esophageal squamous cell carcinoma specimens.Epigenetic regulation of CD271 is associated with chemoresistance and metastatic capacity in esophageal squamous cell carcinoma. PMID: 25351876
45. p75NGFR is a candidate tumor suppressor and has independent prognostic potential in colorectal cancer. PMID: 25244921
46. Case Report: strong p75 staining in cutaneous squamous cell carcinoma. PMID: 25321086
47. Data indicate that leucine-rich repeat neuronal protein 1 (LINGO-1) is intracellular and competes with Nogo-66 receptor (NgR) for binding to p75 neurotrophin receptor (p75NTR). PMID: 25666623
48. Therefore, the 12 selected SNPs may act as tag SNPs for the entire p75NTR gene in Chinese Han population. PMID: 25227100
49. data strongly suggest that CD271 is a crucial determinant of stem-like properties of melanoma cells like colony-formation and tumorigenicity. PMID: 24799129
50. Data are the first to demonstrate that CD271 more specifically identifies the TIC subpopulation within the CD44+ compartment in SCCHN and that this receptor is a functionally active and targetable molecule. PMID: 25149537
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亞細胞定位：

Cell membrane; Single-pass type I membrane protein. Perikaryon. Cell projection, growth cone. Cell projection, dendritic spine.
數據庫鏈接：

HGNC: 7809

OMIM: 162010

KEGG: hsa:4804

STRING: 9606.ENSP00000172229

UniGene: Hs.415768

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