Radixin Antibody (1E12) - Azide and BSA Free
Novus Biologicals | Catalog # H00005962-M01
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Scientific Data Images for Radixin Antibody (1E12) - Azide and BSA Free
Western Blot: Radixin Antibody (1E12) [H00005962-M01]
Western Blot: Radixin Antibody (1E12) [H00005962-M01] - RDX monoclonal antibody (M01), clone 1E12. Analysis of RDX expression in human kidney.Immunocytochemistry/ Immunofluorescence: Radixin Antibody (1E12) [H00005962-M01]
Immunocytochemistry/Immunofluorescence: Radixin Antibody (1E12) [H00005962-M01] - Analysis of monoclonal antibody to RDX on HeLa cell. Antibody concentration 10 ug/ml.Immunocytochemistry/ Immunofluorescence: Radixin Antibody (1E12) [H00005962-M01] -
Immunocytochemistry/ Immunofluorescence: Radixin Antibody (1E12) [H00005962-M01] - Localization studies of ERM proteins, Ebp50 & ErbB2 in SKBR3 cells & protein proximity analysis(A) Confocal microscopy of ERM proteins & Ebp50. Untreated cells were fixed, permeabilized & stained by specific antibodies for endogenous levels of ezrin, radixin & Ebp50 (max. projection). In SKBR3 cells ezrin & radixin strongly colocalizes with Ebp50 at the plasma membrane. (B) Confocal microscopy (single plane section) & (C) 3D-SIM (max. projections) of ErbB2 & Ebp50 localization. In untreated control conditions, ErbB2 shows a strong colocalization with Ebp50 in lamellipodia-like structures at the plasma membrane. (D-F) Analysis of protein proximity by PLA experiments. SKBR3 cells were transfected either with non-targeting control siRNA or ezrin/radixin specific siRNA. Cells were fixed 72 h after transfection & PLA experiments were performed. The depletion of ezrin or radixin strongly reduces the interaction of ErbB2 with Ebp50 (D), Hsp90 (E) & ErbB3 (F). All results are shown as mean +/− SEM (*P < 0.05; ***P < 0.001). Scale bars: 10 μm (A, B), 8 μm (C). Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/27029001), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: Radixin Antibody (1E12) [H00005962-M01] -
Western Blot: Radixin Antibody (1E12) [H00005962-M01] - ERM expression & localization in SKBR3 breast cancer cells(A) Western blot analysis of ERM levels in SKBR3, HeLa & PC3 cells. SKBR3 breast cancer cells do not express moesin. (B) Colocalization of ezrin/radixin & ErbB2 in SKBR3 cells. 3D-SIM of fixed cells, stained for endogenous ERM & ErbB2, shows a high degree of colocalization between the ezrin/radixin & ErbB2 at the plasma membrane (left panel: max. projection; middle: single plane section; right: single channels of insert). Scale bars: 10 μm. (C) Analysis of protein association in SKBR3 cells by proximity ligation assay (PLA). 2 h treatment with 3 μM GA leads to decreased association of ezrin/ErbB2 & radixin/ErbB2. Data is represented as mean +/− SEM (***P < 0.001). (D) Corresponding single plan section of a representative PLA experiment. Fluorescence & DIC pictures of control cells (upper panel) & cell treated for 2 h with geldanamycin (lower panel) are shown. Scale bars: 10 μm. Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/27029001), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Immunocytochemistry/ Immunofluorescence: Radixin Antibody (1E12) [H00005962-M01] -
Immunocytochemistry/ Immunofluorescence: Radixin Antibody (1E12) [H00005962-M01] - ERM expression & localization in SKBR3 breast cancer cells(A) Western blot analysis of ERM levels in SKBR3, HeLa & PC3 cells. SKBR3 breast cancer cells do not express moesin. (B) Colocalization of ezrin/radixin & ErbB2 in SKBR3 cells. 3D-SIM of fixed cells, stained for endogenous ERM & ErbB2, shows a high degree of colocalization between the ezrin/radixin & ErbB2 at the plasma membrane (left panel: max. projection; middle: single plane section; right: single channels of insert). Scale bars: 10 μm. (C) Analysis of protein association in SKBR3 cells by proximity ligation assay (PLA). 2 h treatment with 3 μM GA leads to decreased association of ezrin/ErbB2 & radixin/ErbB2. Data is represented as mean +/− SEM (***P < 0.001). (D) Corresponding single plan section of a representative PLA experiment. Fluorescence & DIC pictures of control cells (upper panel) & cell treated for 2 h with geldanamycin (lower panel) are shown. Scale bars: 10 μm. Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/27029001), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for Radixin Antibody (1E12) - Azide and BSA Free
Immunocytochemistry/ Immunofluorescence
Western Blot
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Background: Radixin
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Additional Radixin Products
Product Documents for Radixin Antibody (1E12) - Azide and BSA Free
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Product Specific Notices for Radixin Antibody (1E12) - Azide and BSA Free
This product is produced by and distributed for Abnova, a company based in Taiwan.
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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Protocols
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- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ELISA Sample Preparation & Collection Guide
- ELISA Troubleshooting Guide
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- How to Run an R&D Systems Quantikine ELISA
- How to Run an R&D Systems Quantikine™ QuicKit™ ELISA
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- ICC for Adherent Cells
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- Quantikine HS ELISA Kit Assay Principle, Alkaline Phosphatase
- Quantikine HS ELISA Kit Principle, Streptavidin-HRP Polymer
- R&D Systems Quality Control Western Blot Protocol
- Sandwich ELISA (Colorimetric) – Biotin/Streptavidin Detection Protocol
- Sandwich ELISA (Colorimetric) – Direct Detection Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: ELISA
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
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