FOXO4 Recombinant Monoclonal Antibody

說明書

中文名稱：

FOXO4重組抗體
貨號：

CSB-RA008839A0HU
規格：

￥1320
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品描述：

FOXO4 Recombinant Monoclonal Antibody（Code: CSB-RA008839A0HU）是一款高特異性抗體，靶向調控細胞周期和應激反應的關鍵轉錄因子FOXO4。FOXO4通過參與PI3K/AKT信號通路調控細胞增殖、凋亡及氧化應激應答，在腫瘤發生、衰老相關機制及代謝性疾病研究中具有重要價值。本抗體采用重組單克隆技術制備，經ELISA驗證具有優異的結合活性和批次穩定性，可精準識別天然構象的FOXO4蛋白。其高靈敏度與低交叉反應性設計，特別適用于體外樣本中FOXO4蛋白水平的定量檢測，例如細胞裂解液或重組蛋白體系中靶標表達的ELISA分析。在科研領域，該產品可為探究FOXO4在細胞衰老調控、癌癥相關信號通路異常以及氧化應激損傷修復機制等方向提供可靠工具，助力疾病分子機制的基礎研究。
Uniprot No.：

P98177
基因名：

FOXO4
別名：

AFX antibody; AFX1 antibody; Afxh antibody; ALL1-fused gene from X chromosome antibody; Fork head domain transcription factor AFX1 antibody; Forkhead box O4 antibody; Forkhead box protein O4 antibody; FOXO 4 antibody; Foxo4 antibody; FOXO4_HUMAN antibody; MGC117660 antibody; MGC120490 antibody; Mixed lineage leukemia; translocated to; 7 antibody; MLLT7 antibody; Myeloid/lymphoid or mixed lineage leukemia (trithorax homolog; Drosophila); translocated to; 7 antibody; Myeloid/lymphoid or mixed lineage leukemia; translocated to; 7 antibody; RGD1561201 antibody
反應種屬：

Human
免疫原：

A synthesized peptide derived from human FOXO4
免疫原種屬：

Homo sapiens (Human)
標記方式：

Non-conjugated
克隆類型：

Monoclonal
抗體亞型：

Rabbit IgG
純化方式：

Affinity-chromatography
克隆號：

1A3
濃度：

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

Rabbit IgG in 10mM phosphate buffered saline , pH 7.4, 150mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol.
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：

Transcription factor involved in the regulation of the insulin signaling pathway. Binds to insulin-response elements (IREs) and can activate transcription of IGFBP1. Down-regulates expression of HIF1A and suppresses hypoxia-induced transcriptional activation of HIF1A-modulated genes. Also involved in negative regulation of the cell cycle. Involved in increased proteasome activity in embryonic stem cells (ESCs) by activating expression of PSMD11 in ESCs, leading to enhanced assembly of the 26S proteasome, followed by higher proteasome activity.
基因功能參考文獻：
1. Study reports that CK1alpha similarly destabilizes FOXO4 in RAS-mutant cells by phosphorylation at serines 265/268. PMID: 28945225
2. In this review, we introduce the regulation of FOXO4 in physiological and pathological conditions. Particularly, the pathophysiological processes and molecular pathways regulated by FOXO4 in the development and progression of cancer are also summarized PMID: 29719213
3. The results of this genomic analysis suggest that low FOXO4 expression is a significant risk factor for epileptic seizures in patients with LGGs and is associated with the seizure outcome. PMID: 28963932
4. NF-kappaB/snail/YY1/RKIP circuitry regulated by FOXO4 were likely involved in miR-150-induced EMT event. PMID: 27976702
5. Negative expression of FoxO3/FoxO4 and lymph node metastasis were the risk factors for the poor prognosis of bladder cancer. PMID: 28554751
6. Knockdown of FOXO4 but not FOXO1 expression decreased proteasome activity. Following neural differentiation, the HD-iPSC-derived neural progenitor cells (NPCs) demonstrated lower levels of proteasome activity and FOXO expressions than their WT counterparts. More importantly, overexpression of FOXO4 but not FOXO1 in HD NPCs dramatically enhanced proteasome activity. PMID: 28973411
7. Results show that a small subset of lymphoma cells surviving treatment with doxorubicin or phenylbutyrate showed stem cell-like properties and resistance to chemotherapeuty. The overexpression of FOXO4 was found in these surviving cells, and DLBCL patients with FOXO4-positive tumor cells had poor prognosis. PMID: 27911272
8. FOXO4 and FOXD3 were shown independently predictive of overall survival in gastric cancer PMID: 27027443
9. FoxO1 and FoxO4 antagonize Tat-mediated transactivation of HIV-1 promoter through the repression of Tat protein expression. PMID: 28699853
10. FOXO4 has an inhibitory effect in clearcell renal carcinoma cells, at least in part through inducing apoptosis via upregulation of Bim in the mitochondria-dependent pathway. PMID: 26780985
11. knockdown of Ku70 inhibited cell proliferation accompanying an increase in p27(kip1) levels through interacting with FOXO4 PMID: 26797321
12. miR-664 functions as an oncogene miRNA and has an important role in promoting human osteosarcoma cell proliferation by suppressing FOXO4 expression. PMID: 26463624
13. The data demonstrated that elevated miR-150 targets FOXO4 expression and therefore regulates multiple genes expression, resulting in cervical cancer cell growth and survival. PMID: 26715362
14. Porphyromonas gingivalis-induced reactive oxygen species activate FOXO transcription factors through JNK signalling, and that FOXO1 controls oxidative stress responses, inflammatory cytokine production and cell survival. PMID: 25958948
15. Cox regression analysis indicated FoxO4 to be an independent prognostic factor in non-small cell lung cancers and suggested that FoxO4 might inhibit the process of EMT in non-small cell lung cancers, and might therefore be a target for therapy. PMID: 24935588
16. FOXOs support the metabolic requirements of normal and tumor cells by promoting IDH1 expression. PMID: 25648147
17. data strongly suggest that increased PI3K/AKT-mediated metastatic invasiveness in CaP is associated with FOXO4 loss, and that mechanisms to induce FOXO4 re-expression might suppress CaP metastatic aggressiveness. PMID: 24983969
18. study demonstrated that miR-1274a prompted gastric cancer cells growth and migration through dampening FOXO4 expression thus provided a potential target for human gastric cancer therapy PMID: 25753202
19. Data indicate that glycogen synthase kinase 3 beta (GSK3beta) and transcription factors FOXO1/3/4 promote hepatoma cell proliferation through type I insulin-like growth factor receptor (IGF-IR). PMID: 25053419
20. FOXO4KD-EPCs injected into the rat ischemic limb brought less apoptosis and more neovascularization than EPCs PMID: 24663349
21. Case Report: CIC-FOXO4 fusion sarcoma is a new type of Ewing-like sarcoma that has a specific genetic signature. PMID: 25007147
22. Our data suggest that loss of FOXO4 expression contributes to gastric cancer growth and metastasis, and it may serve as a potential therapeutic target for gastric cancer. PMID: 24886657
23. Data show that forkhead transcription factor 4 (FoxO4) interacts with sterol regulatory element binding protein (SREBP)2 and hypoxia inducible factor (HIF)2alpha to modulate lanosterol 14alpha demethylase (CYP51) promoter activity. PMID: 24353279
24. Data show that small GTPase RALA regulates formation of a JIP1 (C-Jun-amino-terminal-interacting protein 1) scaffold complex to propagate JNK signaling toward FOXO4 (forkhead box O transcription factor) in response to reactive oxygen species (ROS). PMID: 23770673
25. We find that loss of FOXO4 reduces the potential of hESCs to differentiate into neural lineages. PMID: 23551888
26. Taken together, our findings not only suggest that miR-421 promotes nasopharyngeal carcinoma cell proliferation and anti-apoptosis, but also uncover a novel regulatory mechanism for inactivation of FOXO4 in nasopharyngeal carcinoma. PMID: 23707940
27. Coding mutations within the FOXO4 gene are not associated with premature ovarian failure in women from the Tunisian population. PMID: 22285440
28. demonstrated that adiponectin activated 5'-AMP-activated protein kinase alpha2 isoform, leading to inhibition of mammalian target of rapamycin complex 1 and S6K1. This in turn stabilized insulin receptor substrate-1, driving Akt2-mediated inhibition of FoxO4 PMID: 21454807
29. Inhibition of endogenous FOXO proteins attenuated tetradecanoylphorbol Acetate/PDGF-BB mediated differentiation of neuroblastoma cells. PMID: 22411791
30. Data suggest that expression of cytoplasmic FoxO4 in placenta, fetal membranes, and decidua is altered by parturition/labor, preterm chorioamnionitis, and pro-inflammatory stimuli; silencing of FoxO4 gene initiates apoptosis in placental cell lines. PMID: 22112832
31. Studies indicate that FoxO1, 3 and 4 genes were discovered at the chromosomal breakpoints found in cancers and were initially implicated in cancer. PMID: 21613825
32. identified FOXO4 and PDCD4 as direct and functional targets of miR-499-5p PMID: 21934092
33. FOXO4 may function as a tumor suppressor in the development and progression of colorectal cancer. PMID: 22125836
34. Studies indictet that the mammalian FoxO family consists of FoxO1, 3, 4 and 6 and are regulated by by AKT and 14-3-3 proteins. PMID: 21708191
35. gene study of FOXO4, reveals no association with human longevity in Germans PMID: 21388494
36. Foxo4 may be a useful target for suppression in the treatment of HBV-associated hepatocellular carcinoma cells. PMID: 21567078
37. DEPP is regulated at the level of transcription by FoxO in human vascular endothelial cells PMID: 21510935
38. Tax induces a dose-dependent degradation of FoxO4 by the ubiquitin-proteasome pathway. PMID: 21525355
39. greater in fetal membranes obtained from the supracervical compared to distal site PMID: 20934750
40. structure of the FOXO4-DNA-binding domain (DBD)-DNA complex suggests that both direct water-DNA base contacts and the unique water-network interactions contribute to FOXO-DBD binding to the DNA in a sequence-specific manner PMID: 21123876
41. a conserved critical Ku70 role for FOXO function toward coordination of a survival program PMID: 20570964
42. Findings show that oxidative stress and FOXO4 induce PAI-1 expression through modulation of HIF-1alpha and CREB protein levels and that enhanced CREB binding to the PAI-1 promoter is critical for the PAI-1 induction under oxidative stress. PMID: 20136501
43. FoxO4 acts on CYP51 to regulate the late steps of cholesterol biosynthesis. PMID: 20037138
44. PKG inhibits TCF signaling in colon cancer cells by blocking beta-catenin expression and activating FOXO4. PMID: 20348951
45. these data provide a mechanism of FOXO4 anti-oxidative protection through O-GlcNAcylation. PMID: 19932102
46. The forkhead transcription factor AFX activates apoptosis by induction of the BCL-6 transcriptional repressor. PMID: 11777915
47. AFX zeta is a downstream target of both the phosphatidylinositol 3-kinase/PKB insulin signaling pathway and an AMP-activated protein kinase-dependent pathway. PMID: 11779849
48. Control of cell cycle exit and entry by protein kinase B-regulated forkhead transcription factors PMID: 11884591
49. the MLL-AFX fusion protein requires the transcriptional effector domains of AFX to transform myeloid progenitors and interfere with forkhead protein function PMID: 12192052
50. FOXO4 induces the down-regulation of hypoxia-inducible factor 1 alpha by a von Hippel-Lindau protein-independent mechanism PMID: 12761217
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相關疾病：

A chromosomal aberration involving FOXO4 is found in acute leukemias. Translocation t(X;11)(q13;q23) with KMT2A/MLL1. The result is a rogue activator protein.
亞細胞定位：

Cytoplasm. Nucleus. Note=When phosphorylated, translocated from nucleus to cytoplasm. Dephosphorylation triggers nuclear translocation. Monoubiquitination increases nuclear localization. When deubiquitinated, translocated from nucleus to cytoplasm.
組織特異性：

Heart, brain, placenta, lung, liver, skeletal muscle, kidney and pancreas. Isoform zeta is most abundant in the liver, kidney, and pancreas.
數據庫鏈接：

HGNC: 7139

OMIM: 300033

KEGG: hsa:4303

STRING: 9606.ENSP00000363377

UniGene: Hs.584654

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