1. Neuronal Signaling Stem Cell/Wnt
  2. Notch
  3. Brontictuzumab

Brontictuzumab  (Synonyms: OMP 52M51; Anti-Human NOTCH1 Recombinant Antibody)

目录号: HY-P99258 纯度: 95.00%
COA

Brontictuzumab (OMP 52M51) 是一种单克隆抗体 (MAb),可抑制 Notch1 信号。Brontictuzumab 选择性结合 Notch1 的负调控区域。Brontictuzumab 可抑制肿瘤细胞增殖。Brontictuzumab 可用于白血病和淋巴瘤的研究。

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Brontictuzumab Chemical Structure

Brontictuzumab Chemical Structure

CAS No. : 1447814-75-6

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1 mg ¥3600
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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Brontictuzumab (OMP 52M51) is a monoclonal antibody (MAb) that inhibits Notch1 signal. Brontictuzumab selectively binds the negative regulatory region of the Notch1. Brontictuzumab inhibits tumor cell proliferation. Brontictuzumab can be used in the research of leukemia and lymphoma[1][2][3].

体外研究
(In Vitro)

Brontictuzumab (0-100 μg/mL) inhibits Notch1 signaling, including DLL4, JAG1/2 activity[1].
Brontictuzumab (25 μg/mL, 4 days) reduces the levels of Notch1 intracellular domain in the HPB-ALL cell line[1].
Brontictuzumab (25 μg/mL, 48 h) inhibits DLL4-mediated cleaved-Notch1 overexpression in MCL cells[2].
Brontictuzumab (25 μg/mL, 48 h) blocks the increased phosphorylation of both, MEK and ERK by DLL4 stimulation in Mino cells[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[2]

Cell Line: DLL4 (4 μg/mL)-stimulated MCL cells
Concentration: 25 μg/mL
Incubation Time: 24 or 48 h
Result: Inhibited DLL4-dependent activation of Notch1.
体内研究
(In Vivo)

Brontictuzumab (15 mg/kg, i.p.) reduces tumor burden in T-ALL xenograft[3].
Brontictuzumab (20 mg/kg, i.p., every 4 days) inhibits DLL4 induced activation of Notch1 in MCL model[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: T-ALL xenograft[3]
Dosage: 15 mg/kg
Administration: Intraperitoneal injection (i.p.), twice weekly.
Result: Inhibited tumor growth and reduced the size of the spleen.
Showed massive infiltration and replacement of normal hematopoiesis by leukemia cells.
Animal Model: NSG mice injected with DLL4-stimulated NOTCH1-mutated mino cells ex vivo[2]
Dosage: 20 mg/kg
Administration: Intraperitoneal injection (i.p.)
Result: Inhibited cleaved Notch1 but was not enough to cause a significant efficacy in tumor growth.
Clinical Trial
CAS 号
性状

液体

颜色

Colorless to light yellow

运输条件

Shipping with dry ice.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料

纯度: 95.00%

参考文献

Brontictuzumab 相关分类

  • 摩尔计算器

  • 稀释计算器

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
Brontictuzumab
目录号:
HY-P99258
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