Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
Western blot analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Human placenta tissue lysates,
Lane 2: Hela whole cell lysates,
Lane 3: K562 whole cell lysates,
Lane 4: Caco-2 whole cell lysates,
Lane 5: A549 whole cell lysates,
Lane 6: A431 whole cell lysates,
Lane 7: HEK293 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-GM130/GOLGA2 antigen affinity purified monoclonal antibody (M05865-2) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for GM130/GOLGA2 at approximately 130 kDa. The expected band size for GM130/GOLGA2 is at 113 kDa.
Western blot analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat brain tissue lysates,
Lane 2: Rat liver tissue lysates,
Lane 3: Mouse brain tissue lysates,
Lane 4: Mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-GM130/GOLGA2 antigen affinity purified monoclonal antibody (M05865-2) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for GM130/GOLGA2 at approximately 130 kDa. The expected band size for GM130/GOLGA2 is at 113 kDa.
IHC analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2).
GM130/GOLGA2 was detected in a paraffin-embedded section of human tonsil tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GM130/GOLGA2 Antibody (M05865-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2).
GM130/GOLGA2 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GM130/GOLGA2 Antibody (M05865-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2).
GM130/GOLGA2 was detected in a paraffin-embedded section of rat pancreas tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GM130/GOLGA2 Antibody (M05865-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
Flow cytometry analysis of A431 cell(1:100) DyLight 488 conjugated goat anti-mouse IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was mouse IgG DyLight 488. Unlabelled sample (Red line).
IF analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2).
GM130/GOLGA2 was detected in an immunocytochemical section of U2OS cells. The section was incubated with mouse anti-GM130/GOLGA2 Antibody (M05865-2) at a dilution of 1:100. Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1126) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Western blot analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Human placenta tissue lysates,
Lane 2: Hela whole cell lysates,
Lane 3: K562 whole cell lysates,
Lane 4: Caco-2 whole cell lysates,
Lane 5: A549 whole cell lysates,
Lane 6: A431 whole cell lysates,
Lane 7: HEK293 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-GM130/GOLGA2 antigen affinity purified monoclonal antibody (M05865-2) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for GM130/GOLGA2 at approximately 130 kDa. The expected band size for GM130/GOLGA2 is at 113 kDa.
Western blot analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat brain tissue lysates,
Lane 2: Rat liver tissue lysates,
Lane 3: Mouse brain tissue lysates,
Lane 4: Mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with mouse anti-GM130/GOLGA2 antigen affinity purified monoclonal antibody (M05865-2) at a dilution of 1:1000 and probed with a goat anti-mouse IgG-HRP secondary antibody (Catalog # BA1050). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for GM130/GOLGA2 at approximately 130 kDa. The expected band size for GM130/GOLGA2 is at 113 kDa.
IHC analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2).
GM130/GOLGA2 was detected in a paraffin-embedded section of human tonsil tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GM130/GOLGA2 Antibody (M05865-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2).
GM130/GOLGA2 was detected in a paraffin-embedded section of human mammary cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GM130/GOLGA2 Antibody (M05865-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2).
GM130/GOLGA2 was detected in a paraffin-embedded section of rat pancreas tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was incubated with mouse anti-GM130/GOLGA2 Antibody (M05865-2) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB (Catalog # AR1027) as the chromogen.
Flow cytometry analysis of A431 cell(1:100) DyLight 488 conjugated goat anti-mouse IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was mouse IgG DyLight 488. Unlabelled sample (Red line).
IF analysis of GM130/GOLGA2 using anti-GM130/GOLGA2 antibody (M05865-2).
GM130/GOLGA2 was detected in an immunocytochemical section of U2OS cells. The section was incubated with mouse anti-GM130/GOLGA2 Antibody (M05865-2) at a dilution of 1:100. Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1126) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).