The largest database of trusted experimental protocols

Ab137855

Manufactured by Abcam
Sourced in United Kingdom

Ab137855 is an antibody detection kit. The kit contains the necessary reagents and materials to detect and quantify target proteins in biological samples.

Automatically generated - may contain errors

2 protocols using ab137855

1

Antibody Profiling for Cell Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
The different antibodies used were mouse monoclonal anti-K8 antibody (clone M20, Sigma-Aldrich, Darmstadt, Germany), mouse monoclonal anti-C terminal K8 antibody (clone 1E8, Abcam, Cambridge, UK), rabbit polyclonal anti-C terminal K8 antibody (SAB4501654, Sigma-Aldrich, Darmstadt, Germany), rabbit polyclonal anti-N terminal K8 antibody (ab137855, Abcam, Cambridge, UK), proprietary mouse monoclonal anti-K8 antibodies (clone D-A10 and clone D-D6), mouse monoclonal anti-uPA antibody (ab131433, Abcam, Cambridge, UK), mouse monoclonal anti-plasminogen antibody (ab38157 Abcam, Cambridge, UK), rabbit polyclonal anti-caspase 3 cleaved (Asp 175) antibody for IF analysis (9661, Cell Signaling Technology, Leiden, The Netherlands), rabbit monoclonal anti-cleaved caspase 3 antibody for IHC analysis (clone 5A1E, Cell Signaling Technology, Leiden, The Netherlands), mouse monoclonal anti-caspase 3 and cleaved caspase 3 Alexis antibody for Western blot (WB) analysis (Enzo Life Science, Farmingdale, NY, USA), mouse monoclonal anti-Ku80 antibody (ab3715, Abcam, Cambridge, UK), mouse monoclonal anti-histone H3 antibody (ab1791, Abcam, Cambridge, UK), anti-Na+/K+ ATPase alpha (H3) (SC-48345, Santa Cruz Biotechnology, Santa Cruz, CA, USA) rabbit polyclonal anti-GFP antibody (ab290, Abcam, Cambridge, UK), and mouse monoclonal anti-Ki67 antibody (Clone Mib1, M7240 DAKO, Santa Clara, CA, USA).
+ Open protocol
+ Expand
2

Cell Viability and Apoptosis Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
To investigate cell viability and apoptosis, cells cultured on the scaffold were observed by double staining with fluorescein diacetate (FDA) and propidium iodide (PI). A scanning electron microscope (SEM, JSM-6380LV, JEOL, Tokyo, Japan) was used to visualize the surface features of the scaffold and cells cultured in the scaffold. The samples were visualized with the SEM using an accelerating voltage of 30 kv. For detailed information on SEM sample preparation, see S1 Text. For Immunocytochemistry, the cultures were prepared as previously described [27 (link)]. The primary antibodies used were as follows: polyclonal rabbit anti-cytokeratin 8 antibody (CK8, 1:100, ab137855, Abcam) and monoclonal rat anti-CD44 antibody (1:100, ab119348, Abcam). Then, followed by secondary goat anti-mouse IgG-TRITC (1:1000, ab6786, Abcam), or a goat anti-rabbit IgG-FITC (1:1000, ab7086, Abcam) antibody.
+ 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!