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Rabbit Polyclonal FGFR1 Antibody

  • 中文名: FGFR1抗体
  • 别    名: CEK; FLG; HH2; OGD; ECCL; FLT2; KAL2; BFGFR; CD331; FGFBR; FLT-2; HBGFR; N-SAM; FGFR-1; HRTFDS; bFGF-R-1
货号: IPDX07293
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 1/50-1/200 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 1/5000-1/10000 Human,Mouse,Rat

产品详情

AliasesCEK; FLG; HH2; OGD; ECCL; FLT2; KAL2; BFGFR; CD331; FGFBR; FLT-2; HBGFR; N-SAM; FGFR-1; HRTFDS; bFGF-R-1
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, Rat
ImmunogenFusion protein of human FGFR1
FormulationPurified antibody in PBS with 0.05% sodium azide and 50% glycerol.

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参考文献

以下是关于FGFR1抗体的3篇代表性文献的示例(注:文献信息为示例,实际文献需通过学术数据库检索确认):

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1. **文献名称**:*Targeting FGFR1 with a novel monoclonal antibody inhibits tumor growth in preclinical models*

**作者**:Smith A, et al.

**摘要**:研究报道了一种新型抗FGFR1单克隆抗体的开发,该抗体通过阻断配体结合抑制FGFR1信号通路,在乳腺癌和肺癌的体外及小鼠模型中显著抑制肿瘤增殖和血管生成。

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2. **文献名称**:*FGFR1 antibody-drug conjugate shows efficacy in FGFR1-amplified cancers*

**作者**:Jones B, et al.

**摘要**:该文献描述了一种FGFR1靶向的抗体-药物偶联物(ADC),在FGFR1扩增的胃癌和卵巢癌细胞系中表现出选择性杀伤作用,并通过减少化疗耐药性提高治疗效果。

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3. **文献名称**:*Mechanism of resistance to FGFR1 inhibitors and antibody-based therapeutic strategies*

**作者**:Wang C, et al.

**摘要**:探讨了肿瘤对FGFR1小分子抑制剂的耐药机制,并提出联合使用FGFR1单克隆抗体可恢复耐药细胞对治疗的敏感性,为克服耐药性提供新策略。

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如需具体文献,建议通过PubMed或Web of Science搜索关键词“FGFR1 antibody”或“anti-FGFR1 therapy”获取最新研究。

背景信息

Fibroblast Growth Factor Receptor 1 (FGFR1) is a transmembrane tyrosine kinase receptor that plays a critical role in regulating cell proliferation, differentiation, survival, and angiogenesis by binding to fibroblast growth factors (FGFs). Dysregulation of FGFR1 signaling, through gene amplification, mutations, or overexpression, is implicated in various cancers (e.g., breast, lung, and gastric cancers) and developmental disorders. FGFR1-targeted antibodies are therapeutic agents designed to inhibit aberrant FGFR1 activity by blocking ligand binding, receptor dimerization, or downstream signaling pathways like MAPK and PI3K/AKT. These monoclonal antibodies (e.g., bemarituzumab) often target the extracellular domain of FGFR1. offering specificity to minimize off-target effects. In oncology, FGFR1 antibodies are explored in clinical trials for tumors with FGFR1 alterations, either as monotherapies or in combination with chemotherapy/immunotherapy. Challenges include addressing resistance mechanisms, tumor heterogeneity, and balancing efficacy with toxicity. Beyond therapy, FGFR1 antibodies serve as diagnostic tools to detect receptor overexpression in patient tissues, aiding in biomarker-driven treatment strategies. Their development highlights the growing emphasis on precision medicine to target molecular drivers of disease.

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