Western blot analysis of HMGCR using anti-HMGCR antibody (A00643-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Caco-2 whole cell lysates,
Lane 2: RT4 whole cell lysates,
Lane 3: THP-1 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HMGCR antigen affinity purified polyclonal antibody (A00643-3) 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 HMGCR at approximately 97 kDa. The expected band size for HMGCR is at 97 kDa.
IHC analysis of HMGCR using anti-HMGCR antibody (A00643-3).
HMGCR was detected in a paraffin-embedded section of human breast cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-HMGCR Antibody (A00643-3) 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 HMGCR using anti-HMGCR antibody (A00643-3).
HMGCR was detected in a paraffin-embedded section of human Colorectal adenocarcinoma tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-HMGCR Antibody (A00643-3) 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 HMGCR using anti-HMGCR antibody (A00643-3).
HMGCR was detected in a paraffin-embedded section of human testicular cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-HMGCR Antibody (A00643-3) 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- HMGCR antibody (A00643-3) detected in paraffin-embedded section of human breast cancer tissue. The tissue section were stained using the cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog # BA1032) and counterstained with DAPI (blue).
all(7) 
Flow Cytometry analysis of HEL cells using anti-HMGCR antibody (A00643-3).
Overlay histogram showing HEL cells stained with A00643-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-HMGCR Antibody (A00643-3) at 1:100 dilution for 30 min at 20°C. Fluoro488 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 (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 HMGCR using anti-HMGCR antibody (A00643-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Caco-2 whole cell lysates,
Lane 2: RT4 whole cell lysates,
Lane 3: THP-1 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HMGCR antigen affinity purified polyclonal antibody (A00643-3) 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 HMGCR at approximately 97 kDa. The expected band size for HMGCR is at 97 kDa.
IHC analysis of HMGCR using anti-HMGCR antibody (A00643-3).
HMGCR was detected in a paraffin-embedded section of human breast cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-HMGCR Antibody (A00643-3) 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 HMGCR using anti-HMGCR antibody (A00643-3).
HMGCR was detected in a paraffin-embedded section of human Colorectal adenocarcinoma tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-HMGCR Antibody (A00643-3) 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 HMGCR using anti-HMGCR antibody (A00643-3).
HMGCR was detected in a paraffin-embedded section of human testicular cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-HMGCR Antibody (A00643-3) 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- HMGCR antibody (A00643-3) detected in paraffin-embedded section of human breast cancer tissue. The tissue section were stained using the cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog # BA1032) and counterstained with DAPI (blue).
Flow Cytometry analysis of HEL cells using anti-HMGCR antibody (A00643-3).
Overlay histogram showing HEL cells stained with A00643-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-HMGCR Antibody (A00643-3) at 1:100 dilution for 30 min at 20°C. Fluoro488 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 HMGCR using anti-HMGCR antibody (A00643-3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Caco-2 whole cell lysates,
Lane 2: RT4 whole cell lysates,
Lane 3: THP-1 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HMGCR antigen affinity purified polyclonal antibody (A00643-3) 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 HMGCR at approximately 97 kDa. The expected band size for HMGCR is at 97 kDa.
IHC analysis of HMGCR using anti-HMGCR antibody (A00643-3).
HMGCR was detected in a paraffin-embedded section of human breast cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-HMGCR Antibody (A00643-3) 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 HMGCR using anti-HMGCR antibody (A00643-3).
HMGCR was detected in a paraffin-embedded section of human Colorectal adenocarcinoma tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-HMGCR Antibody (A00643-3) 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 HMGCR using anti-HMGCR antibody (A00643-3).
HMGCR was detected in a paraffin-embedded section of human testicular cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-HMGCR Antibody (A00643-3) 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- HMGCR antibody (A00643-3) detected in paraffin-embedded section of human breast cancer tissue. The tissue section were stained using the cy3-conjugated Anti-rabbit IgG Secondary Antibody (red)(Catalog # BA1032) and counterstained with DAPI (blue).
Flow Cytometry analysis of HEL cells using anti-HMGCR antibody (A00643-3).
Overlay histogram showing HEL cells stained with A00643-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-HMGCR Antibody (A00643-3) at 1:100 dilution for 30 min at 20°C. Fluoro488 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.
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