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Pimurutamab

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Catalog No. T80612Cas No. 2251771-76-1

Pimurutamab (HLX-07) is a glycoengineered humanized IgG1 monoclonal antibody that specifically targets the Epidermal Growth Factor Receptor (EGFR/HER1). By binding to the extracellular domain of EGFR, Pimurutamab blocks ligand (e.g., EGF, TGF-α) binding, inhibiting receptor dimerization and downstream signaling cascades (e.g., RAS/RAF/MEK/ERK). Its optimized glycosylation profile significantly enhances Antibody-Dependent Cell-mediated Cytotoxicity (ADCC) activity. Pimurutamab is developed for treating EGFR-overexpressing solid tumors, such as colorectal cancer and head and neck squamous cell carcinoma, with potentially improved efficacy over cetuximab.

Pimurutamab

Pimurutamab

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Catalog No. T80612Cas No. 2251771-76-1
Pimurutamab (HLX-07) is a glycoengineered humanized IgG1 monoclonal antibody that specifically targets the Epidermal Growth Factor Receptor (EGFR/HER1). By binding to the extracellular domain of EGFR, Pimurutamab blocks ligand (e.g., EGF, TGF-α) binding, inhibiting receptor dimerization and downstream signaling cascades (e.g., RAS/RAF/MEK/ERK). Its optimized glycosylation profile significantly enhances Antibody-Dependent Cell-mediated Cytotoxicity (ADCC) activity. Pimurutamab is developed for treating EGFR-overexpressing solid tumors, such as colorectal cancer and head and neck squamous cell carcinoma, with potentially improved efficacy over cetuximab.
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
Pimurutamab (HLX-07) is a glycoengineered humanized IgG1 monoclonal antibody that specifically targets the Epidermal Growth Factor Receptor (EGFR/HER1). By binding to the extracellular domain of EGFR, Pimurutamab blocks ligand (e.g., EGF, TGF-α) binding, inhibiting receptor dimerization and downstream signaling cascades (e.g., RAS/RAF/MEK/ERK). Its optimized glycosylation profile significantly enhances Antibody-Dependent Cell-mediated Cytotoxicity (ADCC) activity. Pimurutamab is developed for treating EGFR-overexpressing solid tumors, such as colorectal cancer and head and neck squamous cell carcinoma, with potentially improved efficacy over cetuximab.
In vitro
In macrophage-mediated phagocytosis assays using human cancer cell lines, Pimurutamab (ATG-031) (nanomolar concentrations) blocked the CD24-Siglec-10 interaction and significantly enhanced the engulfment of tumor cells [1].
In vivo
In human tumor xenograft models, systemic administration of Pimurutamab (ATG-031) significantly suppressed tumor growth and demonstrated synergistic effects when combined with PD-L1 inhibitors [1].
Reactivity
Human
Application
FACS
Functional assay
Antibody Type
Monoclonal
FormulationSupplied as a sterile solution in a buffered formulation system (e.g., phosphate-, citrate-, or amino acid-based). Please refer to the CoA for lot-specific composition.
Endotoxin<1.0 EU/mg
Related Conjugates and Formulations
Conjucates
Unconjugated
Antigen Details
Uniprot ID
TargetEGFR
Chemical Properties
Cas No.2251771-76-1
Antibody Information
IsotypeIgG1
Storage & Solubility Information
Storagestore at low temperature | store at -20°C | Shipping with blue ice/Shipping at ambient temperature.

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