WB analysis of mouse brain using 10498-1-AP (same clone as 10498-1-PBS)
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
WB analysis of mouse brain using 10498-1-AP (same clone as 10498-1-PBS)
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
WB analysis of human brain using 10498-1-AP (same clone as 10498-1-PBS)
human brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
human brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
WB analysis of mouse brain using 10498-1-AP (same clone as 10498-1-PBS)
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
WB analysis of mouse brain using 10498-1-AP (same clone as 10498-1-PBS)
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
WB analysis of rat brain using 10498-1-AP (same clone as 10498-1-PBS)
rat brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
rat brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
IP experiment of mouse brain using 10498-1-AP (same clone as 10498-1-PBS)
IP result of anti-SNCB (IP:10498-1-AP, 4ug; Detection:10498-1-AP 1:500) with mouse brain tissue lysate 4000ug. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
IP result of anti-SNCB (IP:10498-1-AP, 4ug; Detection:10498-1-AP 1:500) with mouse brain tissue lysate 4000ug. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
IHC staining of human breast cancer using 10498-1-AP (same clone as 10498-1-PBS)
Immunohistochemical analysis of paraffin-embedded human breast cancer using 10498-1-AP (SNCB antibody) at dilution of 1:10 (under 10x lens). This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
Immunohistochemical analysis of paraffin-embedded human breast cancer using 10498-1-AP (SNCB antibody) at dilution of 1:10 (under 10x lens). This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
IF Staining of HepG2 using 10498-1-AP (same clone as 10498-1-PBS)
Immunofluorescent analysis of HepG2 cells, using SNCB antibody 10498-1-AP at 1:25 dilution and Rhodamine-labeled goat anti-rabbit IgG (red). This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
Immunofluorescent analysis of HepG2 cells, using SNCB antibody 10498-1-AP at 1:25 dilution and Rhodamine-labeled goat anti-rabbit IgG (red). This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
The Proteintech guarantee covers Proteintech antibodies in any species and any application, including those not listed on the datasheet. If the antibody doesn’t perform, you can receive a hassle-free refund or credit note.
WB analysis of mouse brain using 10498-1-AP (same clone as 10498-1-PBS)
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
WB analysis of mouse brain using 10498-1-AP (same clone as 10498-1-PBS)
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
WB analysis of human brain using 10498-1-AP (same clone as 10498-1-PBS)
human brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
WB analysis of mouse brain using 10498-1-AP (same clone as 10498-1-PBS)
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
WB analysis of mouse brain using 10498-1-AP (same clone as 10498-1-PBS)
mouse brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
WB analysis of rat brain using 10498-1-AP (same clone as 10498-1-PBS)
rat brain tissue were subjected to SDS PAGE followed by western blot with 10498-1-AP (SNCB antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
IHC Figures
IHC staining of human breast cancer using 10498-1-AP (same clone as 10498-1-PBS)
Immunohistochemical analysis of paraffin-embedded human breast cancer using 10498-1-AP (SNCB antibody) at dilution of 1:10 (under 10x lens). This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
IP Figures
IP experiment of mouse brain using 10498-1-AP (same clone as 10498-1-PBS)
IP result of anti-SNCB (IP:10498-1-AP, 4ug; Detection:10498-1-AP 1:500) with mouse brain tissue lysate 4000ug. This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
IF/ICC Figures
IF Staining of HepG2 using 10498-1-AP (same clone as 10498-1-PBS)
Immunofluorescent analysis of HepG2 cells, using SNCB antibody 10498-1-AP at 1:25 dilution and Rhodamine-labeled goat anti-rabbit IgG (red). This data was developed using the same antibody clone with 10498-1-PBS in a different storage buffer formulation.
The species listed in Tested Reactivity are in-house verified and applicable species. For unlisted species, please refer to the homology analysis of the immunogen sequence and related species. For rabbit polyclonal antibodies, homology >70% is recommended. For mouse monoclonal antibodies and rabbit recombinant antibodies, homology >90% is recommended. Generally, the higher the homology, the greater the applicability. However, there will be certain differences in protein expression in different species, tissues or cells. Therefore, the homology analysis results are for reference only and do not serve as a guarantee.
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Proteintech
SNCB Polyclonal antibody
Catalog Number
10498-1-PBS
Citations
-
Dilutions
Applications
WB, IHC, IF/ICC, IP, Indirect ELISA
Reactivity
human, mouse, rat
Product Guarantee
Covers any species including not listed on datasheet
Covers any applications including not listed on datasheet
