Anti-M Cadherin antibody [EPR25401-63]
- BOND RX™ Validated
- 20ul selling size
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal M Cadherin antibody. Suitable for IHC-P and reacts with Mouse, Rat samples.
View Alternative Names
CAD15_HUMAN, CCAD, CDH 14, CDH 15, CDH 3, CDHM, Cadherin 15, type 1, M cadherin (myotubule), Cadherin 3, Cadherin-14, M-cadherin, MCAD, MRD3, Muscle cadherin, Myotubule cadherin
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-M Cadherin antibody [EPR25401-63] (AB290732)
Immunohistochemical analysis of paraffin-embedded Mouse cerebellum tissue labelling M Cadherin with ab290732 at 1/4000 (0.114 ug/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection) was used. Positive staining on granule cells of mouse cerebellum. The section was incubated with ab290732 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-M Cadherin antibody [EPR25401-63] (AB290732)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labelling M Cadherin with ab290732 at 1/4000 (0.114 ug/ml) followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection) was used. Negative control : no staining on mouse cerebrum. The section was incubated with ab290732 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-M Cadherin antibody [EPR25401-63] (AB290732)
Immunohistochemical analysis of paraffin-embedded rat skeletal muscle tissue labelling M Cadherin with ab290732 at 1/4000 dilution followed by a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection). Positive staining on satellite cells of rat skeletal muscle. The section was incubated with ab290732 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-M Cadherin antibody [EPR25401-63] (AB290732)
Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscle tissue labelling M Cadherin with ab290732 at 1/4000 dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) as a secondary antibody. Positive staining on satellite cells of mouse skeletal muscle. The section was incubated with ab290732 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
Related conjugates and formulations (1)
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Anti-M Cadherin antibody [EPR25401-63] - BSA and Azide free
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
M-Cadherin facilitates cell-cell adhesion which is vital for the proper alignment of muscle cells during development and repair. This protein is a critical component of the adherens junction complex. During muscle regeneration M-Cadherin helps satellite cells to adhere to existing muscle fibers promoting the fusion needed for effective muscle repair. It operates alongside other proteins including β-catenin and α-catenin which link cadherins to the actin cytoskeleton reinforcing structural integrity.
Pathways
Different cellular processes involve M-Cadherin playing a role in the Wnt signaling and Notch signaling pathways. Wnt signaling is significant in muscle development and regeneration. M-Cadherin interacts with β-catenin in this pathway balancing the regulation of cellular adhesion and signaling events. In the Notch signaling pathway M-Cadherin influences satellite cell activation and proliferation helping maintain muscle stem cell populations which are important under conditions requiring muscle repair.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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