Western blot of purified anti-Ezrin antibody (clone CPTC-Ezrin-1). Lane 1: Molecular weight marker; Lane 2: 20 μg of human brain lysate. The blot was incubated with 0.5 μg/mL of the primary antibody overnight at 4°C, followed by incubation with HRP-labeled goat anti-mouse IgG (Cat. No. 405306). Enhanced chemiluminescence was used as the detection system.
Western blot of purified anti-Ezrin antibody (clone CPTC-Ezrin-1). Lane 1: Molecular weight marker; Lane 2: 20 μg of human brain lysate. The blot was incubated with 0.5 μg/mL of the primary antibody overnight at 4°C, followed by incubation with HRP-labeled goat anti-mouse IgG (Cat. No. 405306). Enhanced chemiluminescence was used as the detection system.
Western blot of purified anti-Ezrin antibody (clone CPTC-Ezrin-1). Lane 1: Molecular weight marker; Lane 2: 20 μg of mouse brain lysate; Lane 3: 20 μg of rat brain lysate. The blot was incubated with 0.5 μg/mL of the primary antibody overnight at 4°C, followed by incubation with HRP-labeled goat anti-mouse IgG (Cat. No. 405306). Enhanced chemiluminescence was used as the detection system.
IHC staining of purified anti-Ezrin antibody (clone CPTC-Ezrin-1) on formalin-fixed paraffin-embedded human brain tissue. Following antigen retrieval using Sodium Citrate H.I.E.R., the tissue was incubated with 1 µg/mL of the primary antibody overnight at 4°C. BioLegend’s Ultra Streptavidin (USA) HRP Detection Kit (Multi-Species, DAB, Cat. No. 929901) was used for detection followed by hematoxylin counterstaining, according to the protocol provided. The image was captured with a 40X objective. Scale bar: 50 µm
IHC staining of purified anti-Ezrin antibody (clone CPTC-Ezrin-1) on formalin-fixed paraffin-embedded mouse brain tissue. Following antigen retrieval using Sodium Citrate H.I.E.R., the tissue was incubated with 1 µg/mL of the primary antibody overnight at 4°C. BioLegend's Ultra Streptavidin (USA) HRP Detection Kit (Multi-Species, DAB, Cat. No. 929901) was used for detection followed by hematoxylin counterstaining, according to the protocol provided. The image was captured with a 40X objective. Scale bar: 50 µm
IHC staining of purified anti-Ezrin antibody (clone CPTC-Ezrin-1) on formalin-fixed paraffin-embedded rat brain tissue. Following antigen retrieval using Sodium Citrate H.I.E.R., the tissue was incubated with 1 µg/mL of the primary antibody overnight at 4°C. BioLegend's Ultra Streptavidin (USA) HRP Detection Kit (Multi-Species, DAB, Cat. No. 929901) was used for detection followed by hematoxylin counterstaining, according to the protocol provided. The image was captured with a 40X objective. Scale bar: 50 µm
IHC staining of purified anti-Ezrin antibody (clone CPTC-Ezrin-1) on formalin-fixed paraffin-embedded mouse brain tissue. Following antigen retrieval using Sodium Citrate H.I.E.R., the tissue was incubated with 1 µg/ml of the primary antibody overnight at 4°C, followed by incubation with Alexa Fluor® 647 goat anti-mouse antibody (Cat No. 405322) for one hour at room temperature. Nuclei were counterstained with DAPI. The image was captured with a 40X objective. Scale bar: 50 µm
Ezrin, a member of the ERM (Ezrin-Radixin-Moesin) family, is a linker protein between cytoskeleton and cellular membrane. It has wide temporal and spatial expression, and participates in a variety of cellular processes such as cell adhesion, cell motility, cell-cell communication, and apoptosis. High levels of Ezrin expression promotes tumorigenesis in tissues, including glioblastoma, breast cancer, and colon cancer. Ezrin is also highly expressed in neural stem cells and neuroblasts, where it may function in actin remodeling.
Each lot of this antibody is quality control tested by Western blotting. For Western blotting, the suggested use of this reagent is 0.5 - 5.0 µg per ml. For immunohistochemistry, a concentration range of 1.0 - 10 µg/ml is suggested. It is recommended that the reagent be titrated for optimal performance for each application.
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Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
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