Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/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 CD44 using anti-CD44 antibody (A00052-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human PANC-1 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CD44 antigen affinity purified polyclonal antibody (A00052-2) 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 CD44 at approximately 85 kDa. The expected band size for CD44 is at 82 kDa.
IHC analysis of CD44 using anti-CD44 antibody (A00052-2) .
CD44 was detected in a paraffin-embedded section of human colon tissue. The tissue section was incubated with rabbit anti-CD44 Antibody (A00052-2) 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 CD44 using anti-CD44 antibody (A00052-2) .
CD44 was detected in a paraffin-embedded section of mouse lymphaden tissue. The tissue section was incubated with rabbit anti-CD44 Antibody (A00052-2) 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 CD44 using anti-CD44 antibody (A00052-2) .
CD44 was detected in a paraffin-embedded section of rat colon tissue. The tissue section was incubated with rabbit anti-CD44 Antibody (A00052-2) 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 CD44 using anti-CD44 antibody (A00052-2) .
CD44 was detected in a paraffin-embedded section of rat colon tissue. The tissue section was incubated with rabbit anti-CD44 Antibody (A00052-2) 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.
IF analysis of CD44 using anti-CD44 antibody (A00052-2).
CD44 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-CD44 Antibody (A00052-2) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Flow Cytometry analysis of MCF-7 cells using anti-CD44 antibody (A00052-2).
Overlay histogram showing MCF-7 cells stained with A00052-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD44 Antibody (A00052-2) 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 (Red line) was also used as a control.
Western blot analysis of CD44 using anti-CD44 antibody (A00052-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human PANC-1 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CD44 antigen affinity purified polyclonal antibody (A00052-2) 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 CD44 at approximately 85 kDa. The expected band size for CD44 is at 82 kDa.
IHC analysis of CD44 using anti-CD44 antibody (A00052-2) .
CD44 was detected in a paraffin-embedded section of human colon tissue. The tissue section was incubated with rabbit anti-CD44 Antibody (A00052-2) 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 CD44 using anti-CD44 antibody (A00052-2) .
CD44 was detected in a paraffin-embedded section of mouse lymphaden tissue. The tissue section was incubated with rabbit anti-CD44 Antibody (A00052-2) 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 CD44 using anti-CD44 antibody (A00052-2) .
CD44 was detected in a paraffin-embedded section of rat colon tissue. The tissue section was incubated with rabbit anti-CD44 Antibody (A00052-2) 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 CD44 using anti-CD44 antibody (A00052-2) .
CD44 was detected in a paraffin-embedded section of rat colon tissue. The tissue section was incubated with rabbit anti-CD44 Antibody (A00052-2) 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.
IF analysis of CD44 using anti-CD44 antibody (A00052-2).
CD44 was detected in an immunocytochemical section of A431 cells. The section was incubated with rabbit anti-CD44 Antibody (A00052-2) at a dilution of 1:100. Dylight488-conjugated Anti-rabbit IgG Secondary Antibody (green)(Catalog#BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Flow Cytometry analysis of MCF-7 cells using anti-CD44 antibody (A00052-2).
Overlay histogram showing MCF-7 cells stained with A00052-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD44 Antibody (A00052-2) 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 (Red line) was also used as a control.