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Demcizumab (OMP 21M18) is an anti-DLL4 monoclonal antibody. Demcizumab is a potent Notch pathway inhibitor. Demcizumab is effective in multiple cancer models, both alone and in combination with chemotherapy agents.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
1 mg | In stock | $ 372.00 | |
5 mg | In stock | $ 933.00 | |
10 mg | In stock | $ 1,490.00 |
Description | Demcizumab (OMP 21M18) is an anti-DLL4 monoclonal antibody. Demcizumab is a potent Notch pathway inhibitor. Demcizumab is effective in multiple cancer models, both alone and in combination with chemotherapy agents. |
In vitro |
Demcizumab (0-100 μg/mL) binds to human DLL4 but not to mouse DLL4 and blocks the interaction of DLL4 with the Notch1 receptor in FACS binding assays[3]. Following treatment with Demcizumab at 20 μg/mL for 48 hours, there is a reduction in the mRNA expression of HES1 and DTX1 in PDTALL cells[4]. Demcizumab (0-80 μg/mL, 1, 2, or 3 days) promotes cell death and early apoptosis in PDTALL13 cells[4]. |
In vivo |
Demcizumab (10 mg/kg, i.p., once weekly) in combination with Irinotecan (7.5 mg/kg) demonstrates a significant antitumor effect in KRASWT and KRASMT colorectal cancer xenograft models[2]. Demcizumab, either alone or in combination with Irinotecan (7.5 mg/kg), is effective against OMP-C8 colon tumors[3]. Administration of Demcizumab (20 mg/kg/week, intraperitoneal injection) increases the survival rate of NRG mice injected with irradiated PDTALL13 cells[4]. |
Synonyms | OMP 21M18 |
Molecular Weight | 145.65 (kDa) |
CAS No. | 1243262-17-0 |
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Demcizumab 1243262-17-0 Neuroscience Proteases/Proteasome Stem Cells Gamma-secretase OMP 21M18 inhibitor inhibit