Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
(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 GRP94/HSP90B1 using anti-GRP94/HSP90B1 antibody (BA0930). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A549 whole cell lysates,
Lane 2: human Hela whole cell lysates,
Lane 3: human Jurkat whole cell lysates,
Lane 4: human K562 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GRP94/HSP90B1 antigen affinity purified polyclonal antibody (BA0930) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for GRP94/HSP90B1 at approximately 100 kDa. The expected band size for GRP94/HSP90B1 is at 92 kDa.
IHC analysis of GRP94/HSP90B1 using anti-GRP94/HSP90B1 antibody (BA0930).
GRP94/HSP90B1 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-GRP94/HSP90B1 Antibody (BA0930) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of GRP94/HSP90B1 using anti-GRP94/HSP90B1 antibody (BA0930).
GRP94/HSP90B1 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-GRP94/HSP90B1 Antibody (BA0930) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
ICC analysis of GRP94/HSP90B1 using anti- GRP94/HSP90B1 antibody (BA0930).
GRP94/HSP90B1 was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-GRP94/HSP90B1 Antibody (BA0930) at a dilution of 1:100. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
Western blot analysis of GRP94/HSP90B1 using anti-GRP94/HSP90B1 antibody (BA0930). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A549 whole cell lysates,
Lane 2: human Hela whole cell lysates,
Lane 3: human Jurkat whole cell lysates,
Lane 4: human K562 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GRP94/HSP90B1 antigen affinity purified polyclonal antibody (BA0930) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for GRP94/HSP90B1 at approximately 100 kDa. The expected band size for GRP94/HSP90B1 is at 92 kDa.
IHC analysis of GRP94/HSP90B1 using anti-GRP94/HSP90B1 antibody (BA0930).
GRP94/HSP90B1 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-GRP94/HSP90B1 Antibody (BA0930) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of GRP94/HSP90B1 using anti-GRP94/HSP90B1 antibody (BA0930).
GRP94/HSP90B1 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-GRP94/HSP90B1 Antibody (BA0930) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
ICC analysis of GRP94/HSP90B1 using anti- GRP94/HSP90B1 antibody (BA0930).
GRP94/HSP90B1 was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-GRP94/HSP90B1 Antibody (BA0930) at a dilution of 1:100. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.