• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Parsatuzumab

CAS No. 1312797-14-0

Parsatuzumab ( —— )

产品货号. M36701 CAS No. 1312797-14-0

Parsatuzumab (Anti-EGFL7; RG 7414) 是一种人源化单克隆抗体,作为免疫调节剂与 EGFL7 结合。Parsatuzumab 选择性阻断 EGFL7 与内皮细胞之间的相互作用,可能抑制血管再生,降低血管内皮生长因子 (VEGF) 抑制。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥2028 有现货
5MG ¥3335 有现货
10MG ¥5346 有现货
25MG ¥7718 有现货
50MG ¥10713 有现货
100MG ¥14153 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Parsatuzumab
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Parsatuzumab (Anti-EGFL7; RG 7414) 是一种人源化单克隆抗体,作为免疫调节剂与 EGFL7 结合。Parsatuzumab 选择性阻断 EGFL7 与内皮细胞之间的相互作用,可能抑制血管再生,降低血管内皮生长因子 (VEGF) 抑制。
  • 产品描述
    Parsatuzumab (Anti-EGFL7; RG 7414) is a humanized monoclonal antibody, acts as an immunomodulator and binds to EGFL7. Parsatuzumab selectively blocks the interaction between EGFL7 and endothelial cells, potentially inhibiting vascular regrowth and reducing vascular endothelial growth factor (VEGF) inhibition.
  • 体外实验
    EGFL7 is a vascular-restricted extracellular matrix protein that promotes endothelial cell adhesion and survival.Parsatuzumab (48 h) inhibits cell proliferation and increases apoptosis against patient-derived xenograft (PDX) cells.Cell Viability Assay Cell Line:Patient-derived xenograft (PDX) cells Concentration:/Incubation Time:48 hours Result:Inhibited cell proliferation by 70% from 20%, and resulted in apoptosis increases by 67-87% from 8-17%.
  • 体内实验
    Parsatuzumab (anti-EGFL7) enhances the antiangiogenesis, tumor growth control, and survival associated with antiVEGF monotherapy in several xenograft and genetically engineered murine tumor models. Parsatuzumab (50 mg/kg; i.v.; 3 times per week) targets EGFL7 and inhibits mantle cell lymphoma (MCL) cell growth and prolongs survival in mouse models of MCL.Animal Model:NSG mice injected with Rec1 cells (s.c.)Dosage:50 mg/kg Administration:Intravenous injection; 3 times per week; sacrificed mice when tumor reached end point criteriaResult:Significantly decreased tumor volume than IgG and increased survival of mice.
  • 同义词
    ——
  • 通路
    Angiogenesis
  • 靶点
    VEGFR
  • 受体
    VEGFR
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1312797-14-0
  • 分子量
  • 分子式
    ——
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    ——
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. García-Carbonero R, et al. Randomized Phase II Trial of Parsatuzumab (Anti-EGFL7) or Placebo in Combination with FOLFOX and Bevacizumab for First-Line Metastatic Colorectal Cancer. Oncologist. 2017 Apr;22(4):375-e30.?
产品手册
关联产品
  • Telatinib

    一种口服活性小分子抑制剂,用于生化测定中的 VEGFR-2 (IC50=6 nM)、VEGFR-3 (IC50=4 nM)、PDEGFRα (IC50=15 nM) 和 c-Kit (IC50=1 nM)。

  • Fargesin

    Fargesin 作为一种潜在的 β1AR 拮抗剂,通过 cAMP/PKA 途径可以保护大鼠免受心肌缺血/再灌注损伤。

  • AG-13958

    AG-13958 (AG-013958) 是一种有效的 VEGFR 酪氨酸激酶抑制剂,用于治疗年龄相关性黄斑变性。