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Monoclonal anti n cadherin

Manufactured by Cell Signaling Technology

Monoclonal anti-N-cadherin is a laboratory reagent used to detect and study the expression of the N-cadherin protein in biological samples. N-cadherin is a cell adhesion molecule that plays a role in various cellular processes. This antibody can be used in techniques such as Western blotting, immunohistochemistry, and flow cytometry to identify and quantify the presence of N-cadherin in cells and tissues.

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2 protocols using monoclonal anti n cadherin

1

Western Blot Analysis of Protein Expression

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Cells were lysed in RIPA buffer and proteins (30 μg) were separated on 8–12% SDS/PAGE gel and then transferred onto PVDF membranes (Millipore, Billerica, MA). After blocking membranes with non-fat milk for 1 h at room temperature, they were bred with proper dilutions of primary antibodies overnight at 4 °C. The following antibodies were used: monoclonal anti-GAPDH (Catalogue#5174, 1:5000), monoclonal anti-E-cadherin (Catalogue#3195, 1:1000), monoclonal anti-N-cadherin (Catalogue#13116, 1:1000), monoclonal anti-HIF-1α (Catalogue#36196, 1:1000), and monoclonal anti-Vimentin (Catalogue#5741, 1:1000) were all purchased from Cell signaling Technology; polyclonal anti-MMP2 (Catalog number: 10373–2-AP, 1:500) and polyclonal anti-MMP9 (Catalog number: 10375–2-AP, 1:500) were purchased from Proteintech; polyclonal anti-SMAD5 (ab88559, 1:1000) and polyclonal anti-STAT3 (ab119352, 1:1000) were purchased from Abcam; polyclonal anti-TIMP3 was purchased from ABGENT (70R-9697). Next day anti-mouse or anti-rabbit IgG secondary antibody (Cell signaling Technology, USA) were used for 1 h at the concentration of 1:5000 at room temperature and rinsed 10 min by TBST for 3 times. The bands were visualized using an ECL chemiluminescent detection system (Thermo Fisher Scientific, Rochester. NY).
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2

Western Blot Analysis of Cell Signaling Proteins

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The cell protein lysates were mixed with RIPA lysis buffer supplemented with PMSF and protein loading buffer. Then, the lysates were separated by SDS-polyacrylamide gel electrophoresis and transferred to PVDF membrane. The following antibodies, monoclonal anti-GAPDH (Catalogue #5174, 1:1000), monoclonal anti-E-cadherin (Catalogue #3195, 1:1000), monoclonal anti-N-cadherin (Catalogue#13116, 1:1000), monoclonal smad2/3 (Catalogue#8685T, 1:1000) were purchased from Cell signaling Technology; monoclonal anti-EGR1 (Catalogue#55160, 1:1000) was purchased from abcam; monoclonal anti-samd7 (Catalogue#66478-1-lg, 1:1000) was purchased from proteintech; monoclonal smad2/3-phosphorylation (Catalogue#abs130992, 1:1000) were purchased from Absin; anti-mouse and anti-rabbit IgG secondary antibody were purchased from Cell signaling Technology.
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