Brontictuzumab

CAS No. 1447814-75-6

Brontictuzumab( —— )

Catalog No. M36719 CAS No. 1447814-75-6

Brontictuzumab (OMP 52M5) is a monoclonal antibody that targets Notch1 and inhibits activation of the pathway.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 736 In Stock
10MG 1169 In Stock
25MG 1739 In Stock
50MG 2306 In Stock
100MG 3097 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Brontictuzumab
  • Note
    Research use only, not for human use.
  • Brief Description
    Brontictuzumab (OMP 52M5) is a monoclonal antibody that targets Notch1 and inhibits activation of the pathway.
  • 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.
  • In Vitro
    Brontictuzumab (0-100 μg/mL) inhibits Notch1 signaling, including DLL4, JAG1/2 activity.Brontictuzumab (25 μg/mL, 4 days) reduces the levels of Notch1 intracellular domain in the HPB-ALL cell line.Brontictuzumab (25 μg/mL, 48 h) inhibits DLL4-mediated cleaved-Notch1 overexpression in MCL cells.Brontictuzumab (25 μg/mL, 48 h) blocks the increased phosphorylation of both, MEK and ERK by DLL4 stimulation in Mino cells..Western Blot Analysis 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.Brontictuzumab (20 mg/kg, i.p., every 4?days) inhibits DLL4 induced activation of Notch1 in MCL model.Animal Model:T-ALL xenograftDosage: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 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.
  • Synonyms
    ——
  • Pathway
    Neuroscience
  • Target
    Gamma-secretase
  • Recptor
    Gamma-secretase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1447814-75-6
  • Formula Weight
  • Molecular Formula
    ——
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Ferrarotto R, et al. A phase I dose-escalation and dose-expansion study of brontictuzumab in subjects with selected solid tumors. Ann Oncol. 2018 Jul 1;29(7):1561-1568. ?
molnova catalog
related products
  • RO7185876

    RO7185876 is a selective gamma secretase modulator, which can be used in the study of Alzheimer's disease.

  • γ-Secretase-IN-1

    γ-Secretase-IN-1 is a potent γ-secretase inhibitor that displays partial antiproliferative activity on T-47D cells and inhibits β-amyloid(40), β-amyloid(42), and Notch γ-secretase cleavage.

  • Aβ42-IN-2

    Aβ42-IN-2, a γ-secretase modulator with an IC50 of 6.5 nM for Αβ42, can be used for Alzheimer's disease research .