EGFR Antibody (Matuzumab) - Azide and BSA Free
Novus Biologicals, part of Bio-Techne | Catalog # NBP2-75911
![Immunohistochemistry: EGFR Antibody (Matuzumab) - Azide and BSA Free [NBP2-75911] Immunohistochemistry: EGFR Antibody (Matuzumab) - Azide and BSA Free [NBP2-75911]](https://resources.bio-techne.com/images/products/EGFR-Antibody-Matuzumab-Immunohistochemistry-NBP2-75911-img0002.jpg)
Conjugate
Catalog #
Key Product Details
Species Reactivity
Human
Applications
Block/Neutralize, ELISA, Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunohistochemistry, Western Blot
Label
Unconjugated
Antibody Source
Monoclonal Human IgG1 kappa Clone # Matuzumab
Format
Azide and BSA Free
Concentration
1 mg/ml
Product Specifications
Immunogen
The parental mouse antibody was generated by immunizing BALB/c mice intraperitoneally with A431 cells in phosphate buffered saline (PBS). Later on the humanzied version of the antibody was created by grafting CDRs of the murine antibody onto human constant regions.
Specificity
This antibody binds the extracellular domain III of the human EGFR and does not cross react with murine EGFR. It was also reported that residues S460/G461 in EGFR domain III are essential components of the epitope. This antibody binds at a site distinct from the EGF binding site, preventing conformational re-arrangement required for dimerization. This antibody can only recognize the active form of EGFR. The antibody binds to both glyco- and aglyco receptor forms.
Clonality
Monoclonal
Host
Human
Isotype
IgG1 kappa
Scientific Data Images for EGFR Antibody (Matuzumab) - Azide and BSA Free
Immunohistochemistry: EGFR Antibody (Matuzumab) - Azide and BSA Free [NBP2-75911]
Immunohistochemistry: EGFR Antibody (Matuzumab) [NBP2-75911] - Anti-EGFR staining of formaldehyde fixed paraffin embedded rat stomach tissue, at 40x magnification. The human IgG1-chimeric version of Matuzumab (NBP2-75911) was used to stain samples at a concentration of 5 ug/ml.Immunohistochemistry: EGFR Antibody (Matuzumab) - Azide and BSA Free [NBP2-75911]
Immunohistochemistry: EGFR Antibody (Matuzumab) [NBP2-75911] - Anti-EGFR staining of formaldehyde fixed paraffin embedded mouse skin tissue, at 40x magnification. The human IgG1-chimeric version of Matuzumab (NBP2-75911) was used to stain samples at a concentration of 5 ug/ml.ELISA: EGFR Antibody (Matuzumab) - Azide and BSA Free [NBP2-75911]
ELISA: EGFR Antibody (Matuzumab) [NBP2-75911] - ELISA Plate coated with human EGFR-Fc at a concentration of 5 ug/ml. A 3-fold serial dilution from 100 to 0.1 ng/ml was performed using NBP2-75911. For detection, a 1:4000 dilution of HRP labelled anti-human kappa light chain antibody was used.Applications for EGFR Antibody (Matuzumab) - Azide and BSA Free
Application
Recommended Usage
Block/Neutralize
Optimal dilutions of this antibody should be experimentally determined.
ELISA
Optimal dilutions of this antibody should be experimentally determined.
Flow Cytometry
Optimal dilutions of this antibody should be experimentally determined.
Immunocytochemistry/ Immunofluorescence
Optimal dilutions of this antibody should be experimentally determined.
Immunohistochemistry
Optimal dilutions of this antibody should be experimentally determined.
Western Blot
Optimal dilutions of this antibody should be experimentally determined.
Formulation, Preparation, and Storage
Purification
Protein A purified
Formulation
PBS
Format
Azide and BSA Free
Preservative
0.02% Proclin 300
Concentration
1 mg/ml
Shipping
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Store at 4C for up to 3 months. For longer storage, aliquot and store at -20C.
Background: EGFR
In addition to its role in normal development, EGFR mutations or overexpression is observed in many tumors, including breast cancer, non-small cell lung carcinoma (NSCLC), colon cancer, and more (3-6). Small molecule tyrosine kinase inhibitors (TKIs), like gefitinib, erlotinib, and afatinib, have shown great efficacy in treating patients with EGFR activating mutations, especially for NSCLC (4-6). However, most patients eventually develop acquired resistance to TKIs and thus combination and alternative therapies are in development (4-6). A third-generation TKI, osimertinib, is approved for NSCLC patients with resistance to first-line EGFR TKI treatment (6). Additionally, combination therapies of EGFR TKIs with monoclonal antibody immunotherapies, like anti-PD-L1, are being further investigated in clinical trials (6).
References
1. Roskoski R Jr. Small molecule inhibitors targeting the EGFR/ErbB family of protein-tyrosine kinases in human cancers. Pharmacol Res. 2019; 139:395-411. https://doi.org/10.1016/j.phrs.2018.11.014
2. Sigismund S, Avanzato D, Lanzetti L. Emerging functions of the EGFR in cancer. Mol Oncol. 2018; 12(1):3-20. https://doi.org/10.1002/1878-0261.12155
3. Normanno N, De Luca A, Bianco C, et al. Epidermal growth factor receptor (EGFR) signaling in cancer. Gene. 2006; 366(1):2-16. https://doi.org/10.1016/j.gene.2005.10.018
4. Liu Q, Yu S, Zhao W, Qin S, Chu Q, Wu K. EGFR-TKIs resistance via EGFR-independent signaling pathways. Mol Cancer. 2018; 17(1):53. https://doi.org/10.1186/s12943-018-0793-1
5. Harrison PT, Vyse S, Huang PH. Rare epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer. Semin Cancer Biol. 2020; 61:167-179. https://doi.org/10.1016/j.semcancer.2019.09.015
6. Wu SG, Shih JY. Management of acquired resistance to EGFR TKI-targeted therapy in advanced non-small cell lung cancer. Mol Cancer. 2018; 17(1):38. https://doi.org/10.1186/s12943-018-0777-1
Long Name
Epidermal Growth Factor Receptor
Alternate Names
EGF R, ErbB, ErbB1, HER-1, biosimilar antibody, biosimilars
Gene Symbol
EGFR
Additional EGFR Products
Product Documents for EGFR Antibody (Matuzumab) - Azide and BSA Free
Product Specific Notices for EGFR Antibody (Matuzumab) - Azide and BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
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