
-
Training
-
Custom Training Solutions
-
Self-Paced Courses
-
Instructor-Led Courses
- Flow Cytometry Basic Training
-
Product-Based Training
- FACSAria Product Based Training
- FACSMelody Product-Based Training
- FACSLyric Product-Based Training
- FACSCanto Product-Based Training
- LSRFortessa Product-Based Training
- FACSymphony Product-Based Training
- FACSDuet Product-Based Training
- HTS Product-Based Training
- BD FACSDiscover™ S8 Cell Sorter Product Training
-
Advanced Training
-
Custom Training Solutions
-
Thought Leadership
-
Product News
- Blogs
-
Scientific Publications
-
Events
- CYTO 2022: (ISAC) International Society for the Advancement of Cytometry
- CYTO 2021: (ISAC) International Society for the Advancement of Cytometry
- Assessing Immune Behavioral Response to Bordetella Pertussis Infection in Mice
- Nature Research Academies Workshop 2023
- CYTO 2023: Advancing the World of Cytometry
- EuroFlow Educational Workshop
- Singapore Gene & Cell Therapy Conference 2023
- Nature Research Masterclass 2023
- Novel Approaches to Single-Cell Plant Research: from Real-Time Imaging Cell Sorting to Single-Nuclei Transcriptomics
- Advances in Immune Monitoring Series
- Pre-workshop @ Single Cell Asia Congress
-
Product News
-
- FACSAria Product Based Training
- FACSMelody Product-Based Training
- FACSLyric Product-Based Training
- FACSCanto Product-Based Training
- LSRFortessa Product-Based Training
- FACSymphony Product-Based Training
- FACSDuet Product-Based Training
- HTS Product-Based Training
- BD FACSDiscover™ S8 Cell Sorter Product Training
-
- CYTO 2022: (ISAC) International Society for the Advancement of Cytometry
- CYTO 2021: (ISAC) International Society for the Advancement of Cytometry
- Assessing Immune Behavioral Response to Bordetella Pertussis Infection in Mice
- Nature Research Academies Workshop 2023
- CYTO 2023: Advancing the World of Cytometry
- EuroFlow Educational Workshop
- Singapore Gene & Cell Therapy Conference 2023
- Nature Research Masterclass 2023
- Novel Approaches to Single-Cell Plant Research: from Real-Time Imaging Cell Sorting to Single-Nuclei Transcriptomics
- Advances in Immune Monitoring Series
- Pre-workshop @ Single Cell Asia Congress
- Singapore (English)
-
Change country/language
Old Browser
Your account has been put on hold due to inactivity. To re-activate, check your account information and make all necessary updates.
Looks like you're visiting us from {{countryName}}.
Would you like to remain on the current country site or be redirected to one based on your location?
Your account has been put on hold due to inactivity. To re-activate, check your account information and make all necessary updates.
BD Pharmingen™ Purified Mouse anti-Ezrin (pT567)
Clone J37-954.281.307 (RUO)






Western blot analysis of Ezrin (pT567) in human epidermis. Lysates from control (lanes 1-3) and human epidermal growth factor-treated (lanes 4-6) human A-431 epidermoid carcinoma (Cat. no. 611447 and 611448, respectively) were probed with purified mAb J37-954.281.307 at concentrations of 0.03125 (lanes 1 and 4), 0.0156 (lanes 2 and 5), and 0.0078 µg/ml (lanes 3 and 6). The bands appear as a doublet with Ezrin (pT567) and Radixin (pT564) identifiable at 80 kD and Moesin (pT558) identifiable at 75 kD in the growth factor treated cells.

Ezrin (pT567) staining on human breast cancer. Following antigen retrieval with BD Retrievagen A buffer (Cat. no. 550524), the formalin-fixed paraffin-embedded sections were either left untreated (left column) or treated with a phosphatase to eliminate all phosphorylation (right column). The tissue sections were stained with either purified Mouse anti-Ezrin (Cat. no. 610602 or 610603, top row) or purified Mouse anti-Ezrin (pT567) (bottom row) with Hematoxylin counterstaining. Original magnification: 40X.


BD Pharmingen™ Purified Mouse anti-Ezrin (pT567)

BD Pharmingen™ Purified Mouse anti-Ezrin (pT567)

Purified_blue.png
Regulatory Status Legend
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
Preparation And Storage
Recommended Assay Procedures
Western blot: Please refer to http://www.bdbiosciences.com/pharmingen/protocols/Western_Blotting.shtml
Product Notices
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
Companion Products



Ezrin is a member of the ERM ( E zrin- R adixin- M oesin) family of proteins that can function as a crosslinker between the actin cytoskeleton and the plasma membrane of the cell. Phosphorylation of threonine residues (Thr567 on Ezrin, Thr564 on Radixin and Thr558 on Moesin) has been reported to occur with stimulation of growth factors and is important for cytoskeletal rearrangements. Phosphorylation of Thr567 at the C-terminal F actin-binding domain has been reported to activate the conversion of Ezrin from a dormant soluble form in the cytosol to a membrane- and actin-binding conformation.
In addition to its reactivity to the human species, the peptide used to generate this antibody is either identical or has homology to analogous regions of mouse and rat Ezrin, Radixin and Moesin. The J37-954.281.307 monoclonal antibody has been reported to recognize phosphorylated T567 on active Ezrin in addition to crossreacting on phosphorylated T564 on Radixin and phosphorylated T558 on Moesin.
Development References (3)
-
Gautreau A, Louvard D, Arpin M. Morphogenic effects of ezrin require a phosphorylation-induced transition from oligomers to monomers at the plasma membrane. J Cell Biol. 2000; 150:193-203. (Biology: Western blot, Immunohistochemistry-formalin (antigen retrieval required)). View Reference
-
Gautreau A, Poullet P, Louvard D, Arpin M. Ezrin, a plasma membrane–microfilament linker, signals cell survival through the phosphatidylinositol 3-kinase/Akt pathway. Proc Natl Acad Sci U S A. 1999; 96:7300-7305. (Biology: Western blot, Immunohistochemistry-formalin (antigen retrieval required)). View Reference
-
Tran Quang C, Gautreau A, Arpin M, Treisman R. Ezrin function is required for ROCK-mediated fibroblast transformation by the Net and Dbl oncogenes. EMBO J. 2000; 19:4565-4576. (Biology: Western blot, Immunohistochemistry-formalin (antigen retrieval required)). View Reference
Please refer to Support Documents for Quality Certificates
Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Report a Site Issue
This form is intended to help us improve our website experience. For other support, please visit our Contact Us page.