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Mouse monoclonal anti n cadherin

Manufactured by Merck Group

Mouse monoclonal anti–N-cadherin is a laboratory reagent used in research applications. It is an antibody that specifically binds to the N-cadherin protein, which is a cell adhesion molecule. This antibody can be used for the detection and analysis of N-cadherin expression in various cell and tissue samples.

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2 protocols using mouse monoclonal anti n cadherin

1

Immunostaining of Buccal Mucosa Cells

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Cotton-tipped swabs (Medi-Choice, Mechanicsville, Virginia) were used to collect buccal mucosa cells from 2 siblings with truncating variants in FLNC and from normal control subjects. Each cheek was rubbed with a slight rolling and scraping motion, and the resulting material was smeared on standard microscope slides. Immunostaining of buccal mucosa and myocardial tissue was performed as previously described (24 (link)), and is detailed in the Online Appendix. For immunofluorescence microscopy, antibodies included: mouse monoclonal antiplakoglobin (P8087, Sigma-Aldrich, St. Louis, Missouri), mouse monoclonal anti–connexin 43 (Cx43) (Millipore, Burlington, Massachusetts), mouse monoclonal anti–N-cadherin (Sigma-Aldrich), mouse monoclonal antidesmoplakin (Fitzgerald, Acton, Massachusetts), mouse monoclonal anti–synapse-associated protein 97SAP97 (Santa Cruz, Dallas, Texas), and rabbit polyclonal antiglycogen synthase kinase 3β (GSK3β) (Cell Signaling Technology, Danvers, Massachusetts). Immunostained preparations were analyzed by confocal microscopy (LSM-510, Zeiss, Oberkochen, Germany).
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2

Immunostaining of Buccal Mucosa Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cotton-tipped swabs (Medi-Choice, Mechanicsville, Virginia) were used to collect buccal mucosa cells from 2 siblings with truncating variants in FLNC and from normal control subjects. Each cheek was rubbed with a slight rolling and scraping motion, and the resulting material was smeared on standard microscope slides. Immunostaining of buccal mucosa and myocardial tissue was performed as previously described (24 (link)), and is detailed in the Online Appendix. For immunofluorescence microscopy, antibodies included: mouse monoclonal antiplakoglobin (P8087, Sigma-Aldrich, St. Louis, Missouri), mouse monoclonal anti–connexin 43 (Cx43) (Millipore, Burlington, Massachusetts), mouse monoclonal anti–N-cadherin (Sigma-Aldrich), mouse monoclonal antidesmoplakin (Fitzgerald, Acton, Massachusetts), mouse monoclonal anti–synapse-associated protein 97SAP97 (Santa Cruz, Dallas, Texas), and rabbit polyclonal antiglycogen synthase kinase 3β (GSK3β) (Cell Signaling Technology, Danvers, Massachusetts). Immunostained preparations were analyzed by confocal microscopy (LSM-510, Zeiss, Oberkochen, Germany).
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