Western blotting analysis using L1 cell adhesion molecule antibody (Cat#3421). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with L1 cell adhesion molecule antibody (Cat#3421, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit(Cat#716).
Flow cytometric analysis of L1 cell adhesion molecule expression in HepG2 cells using L1 cell adhesion molecule antibody (Cat#3421, 1:2,000). Green, isotype control; red, L1 cell adhesion molecule.
Immunocytochemical staining of HepG2 cells with L1 cell adhesion molecule antibody (Cat#3421, 1:1,000). Nuclei were stained blue with DAPI; L1 cell adhesion molecule was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and Smart Gain:Medium. Scale bar, 20 μm.
Applications Tested: Western blotting (WB), flow cytometry (FCM), immunocytochemistry (ICC)
Immunogen
Recombinant protein of human L1CAM
Isotype
Mouse IgG1
Storage Buffer
Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
Storage
Store at -20 °C for 1 year.
Recommended Dilutions
Western Blotting (WB):1:500-1:2,500 Flow Cytometry (FCM): 1:200-1:2,000 Immunocytochemistry (ICC): 1:100-1:1,000
Note
This product is for research use only.
Data
Western blotting analysis using L1 cell adhesion molecule antibody (Cat#3421). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with L1 cell adhesion molecule antibody (Cat#3421, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit(Cat#716).
Flow cytometric analysis of L1 cell adhesion molecule expression in HepG2 cells using L1 cell adhesion molecule antibody (Cat#3421, 1:2,000). Green, isotype control; red, L1 cell adhesion molecule.
Immunocytochemical staining of HepG2 cells with L1 cell adhesion molecule antibody (Cat#3421, 1:1,000). Nuclei were stained blue with DAPI; L1 cell adhesion molecule was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and Smart Gain:Medium. Scale bar, 20 μm.
Western blotting analysis using L1 cell adhesion molecule antibody (Cat#3421). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with L1 cell adhesion molecule antibody (Cat#3421, 1:2,500) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit(Cat#716).
Flow cytometric analysis of L1 cell adhesion molecule expression in HepG2 cells using L1 cell adhesion molecule antibody (Cat#3421, 1:2,000). Green, isotype control; red, L1 cell adhesion molecule.
Immunocytochemical staining of HepG2 cells with L1 cell adhesion molecule antibody (Cat#3421, 1:1,000). Nuclei were stained blue with DAPI; L1 cell adhesion molecule was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and Smart Gain:Medium. Scale bar, 20 μm.
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