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

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

Cat. No.: HY-P99258 Purity: 95.00%
COA

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.

For research use only. We do not sell to patients.

Brontictuzumab Chemical Structure

Brontictuzumab Chemical Structure

CAS No. : 1447814-75-6

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Description

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].

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].

MedChemExpress (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.
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].

MedChemExpress (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 No.
Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Brontictuzumab]

Shipping

Shipping with dry ice.

Storage

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

Purity & Documentation

Purity: 95.00%

References
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Brontictuzumab Related Classifications

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    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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