Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunofluorescence (IF): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
Enzyme linked immunosorbent assay (ELISA): | 1:100-1000 |
(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 Emmprin/CD147/BSG using anti-Emmprin/CD147/BSG antibody (A00248-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat heart tissue lysates,
Lane 2: rat kidney tissue lysates,
Lane 3: rat liver tissue lysates,
Lane 4: mouse heart tissue lysates,
Lane 5: mouse kidney tissue lysates,
Lane 6: mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Emmprin/CD147/BSG antigen affinity purified polyclonal antibody (A00248-3) 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 Emmprin/CD147/BSG at approximately 35-60 kDa. The expected band size for Emmprin/CD147/BSG is at 42 kDa.
IHC analysis of Emmprin/CD147/BSG using anti-Emmprin/CD147/BSG antibody (A00248-3).
Emmprin/CD147/BSG was detected in a paraffin-embedded section of mouse colon tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Emmprin/CD147/BSG Antibody (A00248-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Emmprin/CD147/BSG using anti-Emmprin/CD147/BSG antibody (A00248-3).
Emmprin/CD147/BSG was detected in a paraffin-embedded section of mouse kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Emmprin/CD147/BSG Antibody (A00248-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Emmprin/CD147/BSG using anti-Emmprin/CD147/BSG antibody (A00248-3).
Emmprin/CD147/BSG was detected in a paraffin-embedded section of rat kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Emmprin/CD147/BSG Antibody (A00248-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Emmprin/CD147/BSG using anti-Emmprin/CD147/BSG antibody (A00248-3).
Emmprin/CD147/BSG was detected in a paraffin-embedded section of rat testis tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Emmprin/CD147/BSG Antibody (A00248-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IF analysis using anti- emmprin/CD147 Antibody (A00248-3). detected in paraffin-embedded section of mouse colon tissue. The tissue section were stained using the Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green) (Catalog # BA1127) and counterstained with DAPI (blue).
IF analysis using anti- emmprin/CD147 Antibody (A00248-3). detected in paraffin-embedded section of rat colon tissue. The tissue section were stained using the Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green) (Catalog # BA1127) and counterstained with DAPI (blue).
Flow Cytometry analysis of mouse PBMC cells using anti-Emmprin/CD147/BSG antibody (A00248-3).
Overlay histogram showing mouse PBMC cells stained with A00248-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Emmprin/CD147/BSG Antibody (A00248-3) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
Western blot analysis of Emmprin/CD147/BSG using anti-Emmprin/CD147/BSG antibody (A00248-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat heart tissue lysates,
Lane 2: rat kidney tissue lysates,
Lane 3: rat liver tissue lysates,
Lane 4: mouse heart tissue lysates,
Lane 5: mouse kidney tissue lysates,
Lane 6: mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Emmprin/CD147/BSG antigen affinity purified polyclonal antibody (A00248-3) 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 Emmprin/CD147/BSG at approximately 35-60 kDa. The expected band size for Emmprin/CD147/BSG is at 42 kDa.
IHC analysis of Emmprin/CD147/BSG using anti-Emmprin/CD147/BSG antibody (A00248-3).
Emmprin/CD147/BSG was detected in a paraffin-embedded section of mouse colon tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Emmprin/CD147/BSG Antibody (A00248-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Emmprin/CD147/BSG using anti-Emmprin/CD147/BSG antibody (A00248-3).
Emmprin/CD147/BSG was detected in a paraffin-embedded section of mouse kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Emmprin/CD147/BSG Antibody (A00248-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Emmprin/CD147/BSG using anti-Emmprin/CD147/BSG antibody (A00248-3).
Emmprin/CD147/BSG was detected in a paraffin-embedded section of rat kidney tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Emmprin/CD147/BSG Antibody (A00248-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of Emmprin/CD147/BSG using anti-Emmprin/CD147/BSG antibody (A00248-3).
Emmprin/CD147/BSG was detected in a paraffin-embedded section of rat testis tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Emmprin/CD147/BSG Antibody (A00248-3) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.
IF analysis using anti- emmprin/CD147 Antibody (A00248-3). detected in paraffin-embedded section of mouse colon tissue. The tissue section were stained using the Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green) (Catalog # BA1127) and counterstained with DAPI (blue).
IF analysis using anti- emmprin/CD147 Antibody (A00248-3). detected in paraffin-embedded section of rat colon tissue. The tissue section were stained using the Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green) (Catalog # BA1127) and counterstained with DAPI (blue).
Flow Cytometry analysis of mouse PBMC cells using anti-Emmprin/CD147/BSG antibody (A00248-3).
Overlay histogram showing mouse PBMC cells stained with A00248-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Emmprin/CD147/BSG Antibody (A00248-3) at 1:100 dilution for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG at 1:100 dilution used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.