Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunofluorescence (IF): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
(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 anti- SLC4A1/BAND3 antibody (PB9437). The sample well of each lane was loaded with 30ug of sample under reducing conditions.
Lane 1: human K562 whole cell lysates,
Lane 2: human T-47D whole cell lysates.
Use rabbit anti- SLC4A1/BAND3 1:1000, probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog#EK1002). A specific band was detected for SLC4A1/BAND3 at approximately 102KD. The expected band size for SLC4A1/BAND3 is at 102KD.
IHC analysis of Band 3/AE1/SLC4A1 using anti-Band 3/AE1/SLC4A1 antibody (PB9437).
Band 3/AE1/SLC4A1 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-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 Band 3/AE1/SLC4A1 using anti-Band 3/AE1/SLC4A1 antibody (PB9437).
Band 3/AE1/SLC4A1 was detected in a paraffin-embedded section of human placenta tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 Band 3/AE1/SLC4A1 using anti-Band 3/AE1/SLC4A1 antibody (PB9437).
Band 3/AE1/SLC4A1 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-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 Band 3/AE1/SLC4A1 using anti-Band 3/AE1/SLC4A1 antibody (PB9437).
Band 3/AE1/SLC4A1 was detected in frozen section of human placenta tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 Band 3/AE1/SLC4A1 using anti-Band 3/AE1/SLC4A1 antibody (PB9437) .
Band 3/AE1/SLC4A1 was detected in a paraffin-embedded section of human kidney tissue. The tissue section was incubated with rabbit anti-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 Band 3 using anti-Band 3 antibody (PB9437)
Band 3 was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/mL rabbit anti-Band 3 Antibody (PB9437) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
IF analysis of Band 3 using anti-Band 3 antibody (PB9437)
Band 3 was detected in paraffin-embedded section of rat kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/mL rabbit anti-Band 3 Antibody (PB9437) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
Flow Cytometry analysis of K562 cells using anti-Band 3/AE1/SLC4A1 antibody (PB9437).
Overlay histogram showing K562 cells stained with PB9437 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 anti- SLC4A1/BAND3 antibody (PB9437). The sample well of each lane was loaded with 30ug of sample under reducing conditions.
Lane 1: human K562 whole cell lysates,
Lane 2: human T-47D whole cell lysates.
Use rabbit anti- SLC4A1/BAND3 1:1000, probed with a goat anti-rabbit IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog#EK1002). A specific band was detected for SLC4A1/BAND3 at approximately 102KD. The expected band size for SLC4A1/BAND3 is at 102KD.
IHC analysis of Band 3/AE1/SLC4A1 using anti-Band 3/AE1/SLC4A1 antibody (PB9437).
Band 3/AE1/SLC4A1 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-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 Band 3/AE1/SLC4A1 using anti-Band 3/AE1/SLC4A1 antibody (PB9437).
Band 3/AE1/SLC4A1 was detected in a paraffin-embedded section of human placenta tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 Band 3/AE1/SLC4A1 using anti-Band 3/AE1/SLC4A1 antibody (PB9437).
Band 3/AE1/SLC4A1 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-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 Band 3/AE1/SLC4A1 using anti-Band 3/AE1/SLC4A1 antibody (PB9437).
Band 3/AE1/SLC4A1 was detected in frozen section of human placenta tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 Band 3/AE1/SLC4A1 using anti-Band 3/AE1/SLC4A1 antibody (PB9437) .
Band 3/AE1/SLC4A1 was detected in a paraffin-embedded section of human kidney tissue. The tissue section was incubated with rabbit anti-Band 3/AE1/SLC4A1 Antibody (PB9437) 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 Band 3 using anti-Band 3 antibody (PB9437)
Band 3 was detected in paraffin-embedded section of human placenta tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/mL rabbit anti-Band 3 Antibody (PB9437) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
IF analysis of Band 3 using anti-Band 3 antibody (PB9437)
Band 3 was detected in paraffin-embedded section of rat kidney tissues. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution ) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1μg/mL rabbit anti-Band 3 Antibody (PB9437) overnight at 4°C. DyLight488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.
Flow Cytometry analysis of K562 cells using anti-Band 3/AE1/SLC4A1 antibody (PB9437).
Overlay histogram showing K562 cells stained with PB9437 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Band 3/AE1/SLC4A1 Antibody (PB9437) 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.