Can Get Signal®
Immunoreaction Enhancer Solution
Code No. NKB-101T 50 ml x 2
NKB-101 250 ml x 2
NKB-201 250 ml x 1
NKB-301 250 ml x 1
Store at 4ºC
This kit includes the following components. All reagents should be stored at 4ºC, and protected from light.
|Reagent Name||Code No.|
for primary antibody
|50 ml||250 ml||250 ml||-|
for secondary antibody
|50 ml||250 ml||-||250 ml|
Typical reaction flow
Flow chart of western blotting with Can Get Signal®
Flow chart of ELISA with Can Get Signal®
|Experiment 1. Detection of phosphorylated proteins by Western blotting|
Phosphorylated Akt and ERK were detected by Western blotting analysis using Can Get Signal® and a conventional method (TBS-T). As a result, the signal intensities of the target bands obtained with Can Get Signal® were greater than those of the conventional method. The background level of the experiment with Can Get Signal® was also significantly lower than that of the conventional method. The results suggest that Can Get Signal® improves the sensitivity and specificity of Western blotting analysis.
Sample:Cultured bovine adrenal medulla cells
1. Control (H2O)
2. Insulin (1 nM, stimulated for 5 min)
3. Insulin (10 nM, stimulated for 5 min)
4. Insulin (100 nM, stimulated for 5 min)
Primary antibody:Anti Phospho-Akt rabbit polyclonal antibody (1:2,000 dilutioin)
Secondary antibody:Anti rabbit-HRP antibody (1:20,000 dilution)
Primary antibody:Anti Phospho-ERK monoclonal antibody(1:2,000 dilutioin)
Secondary antibody:Anti mouse-HRP antibody (1:20,000 dilution)
Fig.1 Detection of phosphorylated protein kinases (p-Akt, p-ERK1 and p-ERK2) by Western blotting with Can Get Signal® and a conventional method
*The data was kindly provided by Dr. Yanagita from the Department of Pharmacology, Faculty of Medicine, University of Miyazaki.
|Experiment 2. Detection of His-tagged proteins by Western blotting|
His-tagged recombinant proteins were detected with Can Get Signal® and a conventional method (TBS-T). Can Get Signal® showed excellent greater sensitivity than the conventional method.
Primary antibody:Anti his-tag rabbit polyclonal antibody (1:2,000 dilutioin)
Secondary antibody:Anti rabbit-IgG-HRP antibody (1:20,000 dilution)
Fig.2 Detection of His-tagged proteins by Western blotting
|Experiment 3. Detection of His-tagged proteins by ELISA|
Sandwich ELISA (solid phase antibody: anti-ERK2 monoclonal antibody, primary antibody: anti-His tag polyclonal antibody, secondary antibody: anti-rabbit IgG-HRP antibody) was performed to detect his-tagged human MAP kinase (His-ERK2) synthesized by a cell-free protein synthesis system. Can Get Signal® showed an excellent quantitative curve as a function of antigen concentration whereas the conventional method with TBS-T resulted in low signals.
Fig.3 Detection of His-tagged proteins by sandwich ELISA