The largest database of trusted experimental protocols

2 protocols using rabbit anti α smooth muscle actin antibody

1

Protein Expression and Signaling Pathways Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cell lysates were prepared with RIPA buffer (Beyotime). Protein concentration was determined using a BCA Protein Assay kit (Pierce). Samples were separated by SDS‐PAGE, blotted onto polyvinylidene fluoride membranes, and probed with primary antibodies, followed by horseradish peroxidase–conjugated goat antirabbit IgG or goat antimouse IgG (Boster Bio Tec). β‐actin was used as a loading control. The primary antibodies included rabbit antihuman EVL (1:50; Santa Cruz Biotechnology), mouse antihuman endoglin (1:800; BD Biosciences), rabbit anti–phosphorylated Smad1/5 (1:1000; Cell Signaling), rabbit anti–phosphorylated Smad2/3 (1:500; Santa Cruz Biotechnology), rabbit anti–phosphorylated Akt (Ser 473, 1:800; Cell Signaling), rabbit anti‐Akt (1:800; Cell Signaling), rabbit anti–phosphorylated ERK (1:1000; Cell Signaling), rabbit anti‐ERK (1:1000; Cell Signaling), mouse anti‐β‐actin (1:1000; Sigma‐Aldrich), mouse anti‐CD31 antibody (1:1000; Abcam), rabbit anti–α‐smooth muscle actin antibody (1:200; Abcam), mouse anti–β‐catenin antibody (1:1000; Millipore), rabbit anti‐vimentin antibody (1:1000; Abcam). Membranes were developed using an enhanced chemoluminescence system (Clinx Science Instruments).
+ Open protocol
+ Expand
2

Fibroblast and Myofibroblast Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
Isolated cells underwent further characterisation by staining for fibroblast markers in addition to LacZ. Immunofluorescence was conducted by using a rabbit anti-collagen I antibody (Abcam, Cambridge, MA, USA) to stain for collagen type 1-producing fibroblasts and rabbit anti-α-smooth muscle actin antibody (Abcam) for myofibroblasts. Secondary antibody goat anti-rabbit IgG Alexa Fluor 488 (Molecular Probes, Eugene, OR, USA) was used. Slides were viewed by using a fluorescence microscope at the Centre for Microscopy, Characterization and Analysis at the University of Western Australia.
+ 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!