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Anti-hEGFR-hIgG1NQ

Anti-hEGFR-hIgG1NQ Unit size Cat. code Docs Qty Price
Non-glycosylated monoclonal human IgG1 antibody against human EGFR
100 µg
hegfr-mab12
+-
$325.00

Non-glycosylated monoclonal human IgG1 antibody against human EGFR

Anti-hEGFR-hIgG1NQ features a mutated constant region of the human IgG1 isotype and the variable region of cetuximab. Cetuximab is a chimeric human/mouse IgG1 monoclonal antibody that targets EGFR, a cell surface receptor overexpressed in many types of cancer. EGFR is activated by binding specific ligands, including epidermal growth factor and transforming growth factor-α. Activation of EGFR promotes cell proliferation and survival, as well as angiogenesis, leading to tumor growth and metastasis. Binding of cetuximab to EGFR blocks ligand-receptor binding and induces receptor internalization and subsequent degradation. Consequently, it blocks downstream pathways which regulate cell growth and angiogenesis. In addition, it induces cell death through antibody-dependent cell-mediated cytotoxicity (ADCC) [1,2]. Cetuximab has been approved by the FDA for the treatment of metastatic colorectal cancer and metastatic squamous cell carcinoma of the head and neck  [3].

Anti-hEGFR-hIgG1 contains a N-glycosylation mutation of the constant region of the human IgG1 where potential asparagine (N) glycosylation sites are substituted by glutamine (Q) residues resulting in the production of a non-glycosylated antibody. Glycosylation of an antibody has no effect on antigen binding but is essential for Fc receptor-mediated activity [4]. In non-glycosylated antibodies the effector mechanisms mediated through the Fc receptors types (FcγRI, FcγRII, FcγRIII) and the C1q component of complement are severely compromised or ablated [5]. This antibody has been produced in CHO cells and purified by affinity chromatography with protein G.

Applications:  Anti-hEGFR-hIgG1NQ can be used with Anti-hEGFR-hIgG1 to study the impact of effector functions.

 

References:

Kurai J. et al., 2007. Antibody-dependent cellular cytotoxicity mediated by cetuximab against lung cancer cell lines. Clin Cancer Res. 3(5):1552-61.
Kimura H. et al., 2007. Antibody-dependent cellular cytotoxicity of cetuximab against tumor cells with wild-type or mutant epidermal growth factor receptor. Cancer Sci. 98(8):1275-80.
Vincenzi B. et al., 2010. Cetuximab: from bench to bedside. Curr Cancer Drug Targets. 10(1):80-95.
Arnold J. et al., 2007. The impact of glycosylation on the biological function and structure of human immunoglobulins. Annu Rev Immunol 25:21-50.
Jefferis R., 2009. Glycosylation as a strategy to improve antibody-based therapeutics. Nat Rev Drug Discov. 8:226-34.

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Specifications

Specificity: Targets cells expressing human EGFR

Clonality: Monoclonal antibody

Isotype: Human IgG1

Source: CHO cells

Purity: Purified by affinity chromatography with protein G

Quality control:

  • Binding to human EGFR has been tested using flow cytometry.
  • The complete sequence of this antibody has been verified.
  • The absence of bacterial contamination (e.g. lipoproteins and endotoxins) has been confirmed using HEK-Blue™ TLR2 and HEK-Blue™ TLR4 cells.
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Contents

anti-hEGFR-hIgG1NQ antibody is provided azide-free and lyophilized.

  • 100 µg purified anti-hEGFR-hIgG1NQ antibody

room temperature Product is shipped at room temperature

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