Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 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 NOTCH2 using anti-NOTCH2 antibody (A00518-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human U87 whole cell lysates,
Lane 2: human 293T whole cell lysates,
Lane 3: human MCF-7 whole cell lysates,
Lane 4: human SH-SY5Y whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NOTCH2 antigen affinity purified polyclonal antibody (A00518-2) 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 NOTCH2 at approximately 110, 300 kDa. The expected band size for NOTCH2 is at 110 kDa.
IHC analysis of NOTCH2 using anti-NOTCH2 antibody (A00518-2).
NOTCH2 was detected in a paraffin-embedded section of human glioblastoma tissue. The tissue section was incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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 NOTCH2 using anti-NOTCH2 antibody (A00518-2).
NOTCH2 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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 NOTCH2 using anti-NOTCH2 antibody (A00518-2).
NOTCH2 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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 NOTCH2 using anti-NOTCH2 antibody (A00518-2).
NOTCH2 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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 NOTCH2 using anti-NOTCH2 antibody (A00518-2).
NOTCH2 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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.
Flow Cytometry analysis of SH-SY5Y cells using anti-NOTCH2 antibody (A00518-2).
Overlay histogram showing SH-SY5Y cells stained with A00518-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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 without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.
Western blot analysis of NOTCH2 using anti-NOTCH2 antibody (A00518-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human U87 whole cell lysates,
Lane 2: human 293T whole cell lysates,
Lane 3: human MCF-7 whole cell lysates,
Lane 4: human SH-SY5Y whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NOTCH2 antigen affinity purified polyclonal antibody (A00518-2) 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 NOTCH2 at approximately 110, 300 kDa. The expected band size for NOTCH2 is at 110 kDa.
IHC analysis of NOTCH2 using anti-NOTCH2 antibody (A00518-2).
NOTCH2 was detected in a paraffin-embedded section of human glioblastoma tissue. The tissue section was incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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 NOTCH2 using anti-NOTCH2 antibody (A00518-2).
NOTCH2 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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 NOTCH2 using anti-NOTCH2 antibody (A00518-2).
NOTCH2 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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 NOTCH2 using anti-NOTCH2 antibody (A00518-2).
NOTCH2 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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 NOTCH2 using anti-NOTCH2 antibody (A00518-2).
NOTCH2 was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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.
Flow Cytometry analysis of SH-SY5Y cells using anti-NOTCH2 antibody (A00518-2).
Overlay histogram showing SH-SY5Y cells stained with A00518-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NOTCH2 Antibody (A00518-2) 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 without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.