KD25

Western blotting analysis using anti-APBB1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-APBB1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-phospho-CDC6 (Ser106) antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-phospho-CDC6 (Ser106) antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit .

Western blotting analysis using anti-Prolyl endopeptidase like antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Prolyl endopeptidase like antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Brain derived neurotrophic factor antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Brain derived neurotrophic factor antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Syntaxin binding protein 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Syntaxin binding protein 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Vinculin antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Vinculin antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-gli3 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-gli3 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit .

Western blotting analysis using anti-Glutamate-ammonia ligase antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Glutamate-ammonia ligase antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Glutathione synthetase antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Glutathione synthetase antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-TCP1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-TCP1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-G-rich RNA sequence binding factor 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-G-rich RNA sequence binding factor 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-GSK3 α antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-GSK3 α antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-HDAC3 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-HDAC3 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-HSF1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-HSF1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit . HSF1, heat shock transcription factor 1.

Western blotting analysis using anti-Hexokinase 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Hexokinase 1 antibody and HRP-conjugated goat anti rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Histone acetyltransferase 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Histone acetyltransferase 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-IL13 receptor alpha 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-IL13 receptor alpha 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-IMPDH2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-IMPDH2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit .

Western blotting analysis using anti-Insulin receptor antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Insulin receptor antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Integrin subunit alpha V antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Integrin subunit alpha V antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-interferon regulatory factor 6 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-interferon regulatory factor 6 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit .

Western blotting analysis using anti-JUNB antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-JUNB antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-karyopherin subunit alpha 2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-karyopherin subunit alpha 2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit .

Western blotting analysis using anti-Kinesin family member 11 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Kinesin family member 11 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Kinesin family member 23 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Kinesin family member 23 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-kinesin family member 4A antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-kinesin family member 4A antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-kinesin light chain 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-kinesin light chain 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit .

Western blotting analysis using anti-LDL receptor related protein 8 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-LDL receptor related protein 8 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Nectin cell adhesion molecule 2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Nectin cell adhesion molecule 2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-LYN antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-LYN antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Lysine acetyltransferase 7 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Lysine acetyltransferase 7 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-lysyl-tRNA synthetase 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-lysyl-tRNA synthetase 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit .

Western blotting analysis using anti-MAP2K1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-MAP2K1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-MEKK2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-MEKK2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-MAP3K7 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-MAP3K7 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Matrin 3 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Matrin 3 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-MCM7 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-MCM7 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-mTOR antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-mTOR antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-MBD2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-MBD2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-MLD antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-MLD antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-MLKL antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-MLKL antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit . MLKL, Rho associated coiled-coil containing protein kinase 1.

Western blotting analysis using anti-MLKL antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-MLKL antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit . MLKL, mixed lineage kinase domain like pseudokinase.

Western blotting analysis using anti-MOV10 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-MOV10 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-NEK2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-NEK2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-NME1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-NME1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-NHEJ1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-NHEJ1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Nucleoporin 155 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Nucleoporin 155 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Nudix hydrolase 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Nudix hydrolase 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-p150 CAF1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-p150 CAF1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-p38 MAPK antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-p38 MAPK antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .