首页 / 产品 / 抗体 / 一抗

Mouse Monoclonal DLL4 Antibody

  • 中文名: DLL4抗体
  • 别    名: hdelta2
货号: IPD30386
Price: ¥1280
数量:
大包装询价

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 1/200 - 1/1000 Human,Mouse,Rat
ICC 技术咨询 Human,Mouse,Rat
FCM 咨询技术 Human,Mouse,Rat
Elisa 1/10000 Human,Mouse,Rat

产品详情

Aliaseshdelta2
Entrez GeneID54567
clone4A11F8
WB Predicted band size74.6kDa
Host/IsotypeMouse IgG1
Antibody TypePrimary antibody
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Species ReactivityHuman
ImmunogenPurified recombinant fragment of human DLL4 (AA: 313-439) expressed in E. Coli.

FormulationPurified antibody in PBS with 0.05% sodium azide

+ +

参考文献

以下是关于DLL4抗体的3篇参考文献,按您的要求整理如下:

---

1. **标题**: *Inhibition of Dll4 signalling inhibits tumour growth by deregulating angiogenesis*

**作者**: Nogués, L., et al.

**摘要**: 该研究通过动物模型证明,阻断DLL4-Notch信号通路可导致肿瘤血管结构异常增生但功能低下,从而抑制肿瘤生长和转移,为DLL4抗体作为抗血管生成疗法提供理论支持。

2. **标题**: *Targeting DLL4 in tumors shows preclinical activity but potentially significant toxicity*

**作者**: Ridgway, J., et al.

**摘要**: 临床前研究表明,DLL4抗体通过扰乱Notch信号通路抑制肿瘤血管生成,但可能引发严重副作用(如心血管异常),提示治疗需权衡疗效与安全性。

3. **标题**: *Phase I study of DEMCizumab (anti-DLL4) in advanced solid tumors*

**作者**: Smith, D.C., Bekele, B.N., et al.

**摘要**: 首次人体临床试验评估DLL4抗体(DEMCizumab)的安全性,显示部分患者疾病稳定,但剂量限制性毒性(如高血压、心力衰竭)需进一步优化治疗方案。

---

这些文献涵盖基础机制、临床前毒性和早期临床试验,反映了DLL4抗体在肿瘤治疗中的潜力与挑战。如需具体文章链接或扩展内容,可进一步说明。

背景信息

The Delta-like ligand 4 (DLL4) antibody targets DLL4. a key ligand in the Notch signaling pathway, which plays a critical role in regulating cell differentiation, proliferation, and angiogenesis. DLL4 is predominantly expressed in endothelial cells and certain tumor cells, where it binds to Notch receptors (Notch1/Notch4) to coordinate vascular development and maintenance. Its involvement in pathological angiogenesis, particularly in cancers, has made it a therapeutic focus. By blocking DLL4-Notch interactions, DLL4 antibodies inhibit tumor-associated angiogenesis, disrupting the formation of functional vasculature and starving tumors of nutrients. This approach has shown promise in preclinical models of solid tumors, including colorectal and ovarian cancers. However, DLL4 inhibition may also trigger compensatory mechanisms, such as increased VEGF expression, necessitating combination therapies. Beyond oncology, DLL4 antibodies are explored in ischemic diseases to modulate abnormal vessel growth. Current research addresses challenges like on-target toxicity (e.g., vascular hyperplasia) and optimal dosing. Several DLL4-targeting agents, including demcizumab and enoticumab, have entered clinical trials, though efficacy and safety data remain under evaluation. Understanding DLL4's dual roles in physiological and pathological contexts continues to drive innovation in antibody engineering and therapeutic strategies.

客户数据及评论

折叠内容

大包装询价

×