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Rabbit Polyclonal FIR Antibody

  • 中文名: FIR抗体
  • 别    名: FERM; RhoGEF and pleckstrin domain protein 2; FGD1-related Cdc42-GEF; FIR; FRG
货号: IPDX41887
Price: ¥1180
数量:
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验证与应用

应用及物种
WB 咨询技术 Human,Mouse,Rat
IF 咨询技术 Human,Mouse,Rat
IHC 咨询技术 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 咨询技术 Human,Mouse,Rat

产品详情

AliasesFERM; RhoGEF and pleckstrin domain protein 2; FGD1-related Cdc42-GEF; FIR; FRG
Entrez GeneID9855;
WB Predicted band size119kDa
Host/IsotypeRabbit IgG
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman,Mouse
ImmunogenSynthesized peptide derived from Internal of human FIR.
FormulationPurified antibody in PBS with 0.05% sodium azide.

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参考文献

以下是关于FIR抗体的3篇参考文献及其摘要概述:

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1. **文献名称**:*"Autoantibody against DNA replication factor FIR (FBP-interacting repressor) in esophageal squamous cell carcinoma"*

**作者**:Sugito, K. et al.

**摘要**:该研究在食管鳞状细胞癌患者血清中发现FIR抗体,揭示了其作为潜在肿瘤标志物的价值。FIR蛋白参与细胞周期调控,其抗体可能反映肿瘤发生中的异常DNA复制过程。

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2. **文献名称**:*"FBP-interacting repressor (FIR) suppresses transcriptional activity of the c-MYC promoter by directly binding to DNA"*

**作者**:Kojima, T. et al.

**摘要**:研究利用FIR抗体通过染色质免疫沉淀(ChIP)技术,证实FIR通过结合c-MYC启动子抑制其转录活性,揭示了其在癌症中调控原癌基因表达的分子机制。

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3. **文献名称**:*"FIR regulates expression of genes involved in proliferation and metastasis in colorectal cancer cells"*

**作者**:Nakamura, Y. et al.

**摘要**:通过FIR抗体介导的蛋白质检测,研究发现FIR在结直肠癌细胞中调控增殖和转移相关基因(如MMP9),提示其可能成为癌症治疗的潜在靶点。

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这些文献均通过FIR抗体探索了该蛋白在癌症中的功能机制及临床价值。如需具体文章,可通过PubMed或Sci-Hub输入标题获取全文。

背景信息

FIR (FBP Interacting Repressor) antibodies are essential tools for studying the multifaceted roles of the FIR protein, a critical regulator of gene expression. Initially identified as a transcriptional repressor interacting with the Far Upstream Element-Binding Protein (FBP), FIR modulates c-MYC expression by competing with FBP for binding to the FUSE element in the c-MYC promoter. This interaction highlights FIR's involvement in cell proliferation and oncogenesis, particularly in cancers like colorectal carcinoma, where its dysregulation is observed. Beyond transcription, FIR (also known as PUF60 or Siah-BP1) functions as a splicing factor, influencing mRNA processing and maintaining genomic stability. It interacts with proteins such as p53 and Siah-1. linking it to apoptosis and stress response pathways. FIR antibodies enable researchers to investigate its expression patterns, subcellular localization, and protein-protein interactions through techniques like Western blotting, immunohistochemistry, and immunoprecipitation. Recent studies explore FIR's dual roles in tumor suppression and progression, as well as its potential implications in neurodegenerative disorders. These antibodies are pivotal for unraveling FIR's context-dependent mechanisms in development, disease, and therapeutic targeting.

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