DLL4 (蛋白 | 抗体 | cDNA 克隆 | ELISA 试剂盒)

All DLL4 reagents are produced in house and quality controlled, including 10 DLL4 Antibody, 4 DLL4 ELISA, 27 DLL4 Gene, 5 DLL4 Lysate, 5 DLL4 Protein, 2 DLL4 qPCR. All DLL4 reagents are ready to use.

DLL4 Protein (5)

DLL4 Antibody (10)

DLL4 ELISA 试剂盒(即用型)& ELISA 抗体对套装(非即用型)(4)

DLL4 cDNA Clone (27)

NM_019074.2

克隆载体 cDNA 产品

In lentiviral vector

NM_019454.3

克隆载体 cDNA 产品

In lentiviral vector

XM_005559226.2

克隆载体 cDNA 产品

DLL4 Lysate (5)

DLL4 分子背景

Delta-like protein 4 (DLL4, Delta4), a type I membrane-bound Notch ligand, is one of five known Notch ligands in mammals and interacts predominantly with Notch 1, which has a key role in vascular development. Recent studies yield substantial insights into the role of DLL4 in angiogenesis. DLL4 is induced by vascular endothelial growth factor (VEGF) and acts downstream of VEGF as a 'brake' on VEGF-induced vessel growth, forming an autoregulatory negative feedback loop inactivating VEGF. DLL4 is downstream of VEGF signaling and its activation triggers a negative feedback that restrains the effects of VEGF. Attenuation of DLL4/Notch signaling results in chaotic vascular network with excessive branching and sprouting. DLL4 is widely distributed in tissues other than vessels including many malignancies. Furthermore, the molecule is internalized on binding its receptor and often transported to the nucleus. In pathological conditions, such as cancer, DLL4 is up-regulated strongly in the tumour vasculature. Blockade of DLL4-mediated Notch signaling strikingly increases nonproductive angiogenesis, but significantly inhibits tumor growth in preclinical mouse models. In preclinical studies, blocking of DLL4/Notch signaling is associated with a paradoxical increase in tumor vessel density, yet causes marked growth inhibition due to functionally defective vasculature. Thus, DLL4 blockade holds promise as an additional strategy for angiogenesis-based cancer therapy.

DLL4 参考文献

  • Yan M, et al. (2007) Delta-like 4/Notch signaling and its therapeutic implications. Clin Cancer Res. 13(24): 7243-6.
  • Sainson RC, et al. (2007) Anti-Dll4 therapy: can we block tumour growth by increasing angiogenesis? Trends Mol Med. 13(9): 389-95.
  • Martinez JC, et al. (2009) Nuclear and membrane expression of the angiogenesis regulator delta-like ligand 4 (DLL4) in normal and malignant human tissues. Histopathology. 54(5): 598-606.
  • Li JL, et al. (2010) Targeting DLL4 in tumors shows preclinical activity but potentially significant toxicity. Future Oncol. 6(7): 1099-103.