Western blotting analysis using alpha glucosidase antibody (Cat#61383). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with alpha glucosidase antibody (Cat#61383, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Western blotting analysis using alpha glucosidase antibody (Cat#61383). alpha glucosidase expression in wild type (WT) and alpha glucosidase (GAA) knockdown (KD) HSHC cells with 20 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with alpha glucosidase antibody (Cat#61383, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Flow cytometric analysis of alpha glucosidase expression in HepG2 cells using alpha glucosidase antibody (Cat#61383, 1:2,000). Green, isotype control; red, alpha glucosidase.
Immunohistochemistry was performed on paraffin-embedded human pancreatic adenocarcinoma using alpha glucosidase antibody (Cat#61383, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar, 25 μm.
Western blotting analysis using alpha glucosidase antibody (Cat#61383). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with alpha glucosidase antibody (Cat#61383, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Western blotting analysis using alpha glucosidase antibody (Cat#61383). alpha glucosidase expression in wild type (WT) and alpha glucosidase (GAA) knockdown (KD) HSHC cells with 20 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with alpha glucosidase antibody (Cat#61383, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Flow cytometric analysis of alpha glucosidase expression in HepG2 cells using alpha glucosidase antibody (Cat#61383, 1:2,000). Green, isotype control; red, alpha glucosidase.
Immunohistochemistry was performed on paraffin-embedded human pancreatic adenocarcinoma using alpha glucosidase antibody (Cat#61383, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar, 25 μm.
Western blotting analysis using alpha glucosidase antibody (Cat#61383). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with alpha glucosidase antibody (Cat#61383, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Western blotting analysis using alpha glucosidase antibody (Cat#61383). alpha glucosidase expression in wild type (WT) and alpha glucosidase (GAA) knockdown (KD) HSHC cells with 20 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with alpha glucosidase antibody (Cat#61383, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Flow cytometric analysis of alpha glucosidase expression in HepG2 cells using alpha glucosidase antibody (Cat#61383, 1:2,000). Green, isotype control; red, alpha glucosidase.
Immunohistochemistry was performed on paraffin-embedded human pancreatic adenocarcinoma using alpha glucosidase antibody (Cat#61383, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar, 25 μm.
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