The largest database of trusted experimental protocols

Anti n cadherin antibody

Manufactured by Merck Group

The Anti-N-cadherin antibody is a laboratory reagent used in various research applications. It is a monoclonal antibody that specifically binds to the N-cadherin protein, which is involved in cell-cell adhesion. The antibody can be used for the detection and analysis of N-cadherin in biological samples.

Automatically generated - may contain errors

3 protocols using anti n cadherin antibody

1

Blocking Cellular Interactions in VSMC Mechanics

Check if the same lab product or an alternative is used in the 5 most similar protocols
To perform blocking studies, 5 different media conditions were used: (i) regular VSMC media, (ii) VSMC media with 50
μg/ml anti-integrin β1 antibody (Fisher), (iii) VSMC media with 50 μg/ml anti-N-cadherin antibody
(Sigma-Aldrich), (iv) VSMC media with 50 μg/ml of anti-integrin β1 antibody and 50 μg/ml of anti-N-cadherin
antibody (both antibodies), and (v) VSMC media with 50 μg/ml of non-immune IgG (Sigma-Aldrich). non-immune IgG was used as
a negative control as it was not expected to affect cellular interactions and mechanical properties. The antibody concentration of
50 μg/ml was chosen as it has been shown to be effective blocking concentration in other studies (Mendrick and Kelly, 1993 (link); Sun et al., 2005 (link); Yiin et al., 2009 (link)). Cells were exposed to different media conditions as soon as they were seeded on the
substrate and were maintained in culture for a period of 5 days after which AFM nanoindentation studies were performed to study
mechanical properties. This culture period was selected as VSMCs have been shown previously to stiffen in the first 3–5
days of culture (Hemmer et al., 2008 , Hemmer et al.,
2009
). After this initial stiffening period, cell mechanical properties remain stable for 7–10 days (Hemmer et al. 2009 , Deitch et al. 2012 (link)).
+ Open protocol
+ Expand
2

Immunostaining of Surface and Total N-cadherin in Primary Cortical Neurons

Check if the same lab product or an alternative is used in the 5 most similar protocols
Primary cortical neurons (2 DIV) were washed with ice‐cold PBS and fixed with 4% PFA in PBS for 20 min on ice. After two washes with PBS, cells were blocked with DS‐PBS for 30 min at RT and incubated with diluted primary antibody (anti‐N‐cadherin antibody [C3865, Sigma] for surface N‐cadherin staining) in DS‐PBS for 60 min at RT. After three washes in PBS, cells were permeabilized with DS‐PBS containing 0.15% Triton X‐100 for 5 min at RT, and incubated with diluted primary antibodies (anti‐N‐cadherin antibody [sc‐7939, Santa Cruz Biotechnology] for total N‐cadherin and anti‐GFP chick antibody [AB16901, Millipore]) in DS‐PBT at 4°C overnight. Secondary antibodies were applied as described above. After three washes in PBS, cells were treated with Alexa488‐ or Alexa555‐conjugated secondary antibodies (Molecular Probes) diluted in PBS for 60 min at RT, followed by three washes in PBS.
+ Open protocol
+ Expand
3

N-Cadherin Antibody Inhibition Assay

Check if the same lab product or an alternative is used in the 5 most similar protocols
Tumor cells were blocked with a monoclonal anti-N-cadherin antibody produced in mouse (sigma-aldrich). After 24 hours of incubation, the culture medium was exchanged for the antibody mix with a concentration of 10 μg/ml. In addition, 10 μl antibody (IgG concentration 2–2.5 mg/ml) was mixed with 2ml culture medium. The cells were incubated for 1 h, 12 h, 24 h, or 48 h.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!