The largest database of trusted experimental protocols

2 protocols using anti phospho myosin light chain

1

Antibody Characterization for Cellular Immunostaining

Check if the same lab product or an alternative is used in the 5 most similar protocols
Mouse monoclonal anti-Scribble (sc -55,543), anti-β-Actin (sc -69,879), anti-α E-catenin (sc-9988) (for immuno-staining) and anti-E-cadherin (sc-8426) (for immunoprecipitation) were from Santa Cruz Biotechnology. Antibodies specific for the N- and C-terminal region of Lgl1 were generated in rabbits [30 (link)]. Recombinant GFP antibodies were generated in rabbits [41 (link)]. Antibody specific for the C-terminal region of human NMII-A was generated in rabbits according to the method of [42 (link)]. Mouse monoclonal anti-E-cadherin (ab1416), anti-His (ab18184) and IgG (ab46540) were obtained from Abcam. Rabbit polyclonal anti-α E-catenin (C2081) was from Sigma. Rabbit polyclonal anti-phospho-Myosin Light Chain 2 (Thr18/Ser19) (3674), anti-Lgl1 (D2B5A), anti-E-Cadherin (24E10) (for immuno-staining), anti-β-catenin (D10A8), and anti-Vimentin (D21H3) were obtained from Cell Signaling Technology. Anti-MBP (E8032) was from New England BioLAbs.
Horseradish peroxidase-conjugated goat anti-Rabbit secondary antibody, donkey anti-Goat conjugated to Alexa Fluor 488 and goat anti-Rabbit conjugated to Cy5 were obtained from Jackson ImmunoResearch Laboratories. Horseradish peroxidase-conjugated goat anti-Mouse (ab6789) and donkey anti-Mouse IgG H&L (Alexa Fluor 555) (ab150110) were obtained from Abcam. All antibodies were diluted 1:1000 for Western blot and 1:100 for immunofluorescence.
+ Open protocol
+ Expand
2

Cytoskeletal Protein Visualization Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
The following primary antibodies were used (dilution is indicated for immunofluorescence unless stated otherwise): anti-α-actinin (ab18061, Abcam, 1:100 dilution), anti-HA (3F10, Sigma-Aldrich, 1:200 dilution), anti-vinculin (#V9131, Sigma-Aldrich, 1:400 dilution), anti-zyxin (sc-6437, Santa Cruz, 1:40 dilution), anti-talin (#T3287, Sigma-Aldrich, 1:100 dilution), anti-β-actin (#MCA5775GA, Bio-Rad Laboratories, 1:200 dilution, 1:2000 for western blot), anti-γ-actin (#MCA5776GA, Bio-Rad Laboratories, 1:200 dilution, 1:2000 for western blot), anti-actin (#A2066, Sigma-Aldrich, 1:5000 dilution for western blot), anti-myosin IIA (#909802, BioLegend, 1:100 dilution), and anti-phospho-myosin light chain (#3671, Cell Signalling Technology, 1:100 dilution). Secondary antibodies conjugated to Alexa647, Alexa555, or Alexa568 were used (Life Technologies, 1:400 dilution). Actin was stained with Alexa488/Alexa633-conjugated phalloidin (Life Technologies, 1:200 dilution). Blebbistatin was purchased from Sigma-Aldrich (#B0560, 50 μM for 60 min).
+ 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!