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 KCNA1 using anti-KCNA1 antibody (A01813-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates,
Lane 2: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-KCNA1 antigen affinity purified polyclonal antibody (A01813-1) 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 KCNA1 at approximately 56,90 kDa. The expected band size for KCNA1 is at 56 kDa.
IHC analysis of KCNA1 using anti-KCNA1 antibody (A01813-1) .
KCNA1 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-KCNA1 Antibody (A01813-1) 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 KCNA1 using anti-KCNA1 antibody (A01813-1) .
KCNA1 was detected in a paraffin-embedded section of human glioma tissue. The tissue section was incubated with rabbit anti-KCNA1 Antibody (A01813-1) 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 KCNA1 using anti-KCNA1 antibody (A01813-1).
KCNA1 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-KCNA1 Antibody (A01813-1) 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).
IF analysis of KCNA1 using anti-KCNA1 antibody (A01813-1).
KCNA1 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-KCNA1 Antibody (A01813-1) 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 Raji cells using anti-KCNA1 antibody (A01813-1).
Overlay histogram showing Raji cells stained with A01813-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-KCNA1 Antibody (A01813-1) 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 KCNA1 using anti-KCNA1 antibody (A01813-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat brain tissue lysates,
Lane 2: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-KCNA1 antigen affinity purified polyclonal antibody (A01813-1) 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 KCNA1 at approximately 56,90 kDa. The expected band size for KCNA1 is at 56 kDa.
IHC analysis of KCNA1 using anti-KCNA1 antibody (A01813-1) .
KCNA1 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-KCNA1 Antibody (A01813-1) 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 KCNA1 using anti-KCNA1 antibody (A01813-1) .
KCNA1 was detected in a paraffin-embedded section of human glioma tissue. The tissue section was incubated with rabbit anti-KCNA1 Antibody (A01813-1) 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 KCNA1 using anti-KCNA1 antibody (A01813-1).
KCNA1 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-KCNA1 Antibody (A01813-1) 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).
IF analysis of KCNA1 using anti-KCNA1 antibody (A01813-1).
KCNA1 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-KCNA1 Antibody (A01813-1) 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 Raji cells using anti-KCNA1 antibody (A01813-1).
Overlay histogram showing Raji cells stained with A01813-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-KCNA1 Antibody (A01813-1) 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.