WB analysis using 16386-1-AP (same clone as 16386-1-PBS)
Various lysates were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:6000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
Various lysates were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:6000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
WB analysis of HepG2 using 16386-1-AP (same clone as 16386-1-PBS)
HepG2 cells were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
HepG2 cells were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
WB analysis of human liver using 16386-1-AP (same clone as 16386-1-PBS)
human liver tissue were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
human liver tissue were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
WB analysis of human heart using 16386-1-AP (same clone as 16386-1-PBS)
human heart tissue were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
human heart tissue were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
WB analysis of HeLa using 16386-1-AP (same clone as 16386-1-PBS)
HeLa cells were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
HeLa cells were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
WB analysis of human liver using 16386-1-AP (same clone as 16386-1-PBS)
human liver tissue were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
human liver tissue were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
IP experiment of HepG2 using 16386-1-AP (same clone as 16386-1-PBS)
IP result of anti-RPL23A (IP:16386-1-AP, 4ug; Detection:16386-1-AP 1:500) with HepG2 cells lysate 3200ug. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
IP result of anti-RPL23A (IP:16386-1-AP, 4ug; Detection:16386-1-AP 1:500) with HepG2 cells lysate 3200ug. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
IHC staining of human colon using 16386-1-AP (same clone as 16386-1-PBS)
Immunohistochemical analysis of paraffin-embedded human normal colon slide using 16386-1-AP (RPL23A antibody) at dilution of 1:1200 (under 20x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
Immunohistochemical analysis of paraffin-embedded human normal colon slide using 16386-1-AP (RPL23A antibody) at dilution of 1:1200 (under 20x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
IHC staining of human colon using 16386-1-AP (same clone as 16386-1-PBS)
Immunohistochemical analysis of paraffin-embedded human normal colon slide using 16386-1-AP (RPL23A antibody) at dilution of 1:1200 (under 20x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
Immunohistochemical analysis of paraffin-embedded human normal colon slide using 16386-1-AP (RPL23A antibody) at dilution of 1:1200 (under 20x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
IF Staining of HepG2 using 16386-1-AP (same clone as 16386-1-PBS)
Immunofluorescent analysis of HepG2 cells using 16386-1-AP (RPL23A antibody) at dilution of 1:50 and Alexa Fluor 488-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L). This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
Immunofluorescent analysis of HepG2 cells using 16386-1-AP (RPL23A antibody) at dilution of 1:50 and Alexa Fluor 488-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L). This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
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WB analysis using 16386-1-AP (same clone as 16386-1-PBS)
Various lysates were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:6000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
WB analysis of HepG2 using 16386-1-AP (same clone as 16386-1-PBS)
HepG2 cells were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
WB analysis of human liver using 16386-1-AP (same clone as 16386-1-PBS)
human liver tissue were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
WB analysis of human heart using 16386-1-AP (same clone as 16386-1-PBS)
human heart tissue were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
WB analysis of HeLa using 16386-1-AP (same clone as 16386-1-PBS)
HeLa cells were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
WB analysis of human liver using 16386-1-AP (same clone as 16386-1-PBS)
human liver tissue were subjected to SDS PAGE followed by western blot with 16386-1-AP (RPL23A antibody) at dilution of 1:0 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
IHC Figures
IHC staining of human colon using 16386-1-AP (same clone as 16386-1-PBS)
Immunohistochemical analysis of paraffin-embedded human normal colon slide using 16386-1-AP (RPL23A antibody) at dilution of 1:1200 (under 20x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
IHC staining of human colon using 16386-1-AP (same clone as 16386-1-PBS)
Immunohistochemical analysis of paraffin-embedded human normal colon slide using 16386-1-AP (RPL23A antibody) at dilution of 1:1200 (under 20x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
IP Figures
IP experiment of HepG2 using 16386-1-AP (same clone as 16386-1-PBS)
IP result of anti-RPL23A (IP:16386-1-AP, 4ug; Detection:16386-1-AP 1:500) with HepG2 cells lysate 3200ug. This data was developed using the same antibody clone with 16386-1-PBS in a different storage buffer formulation.
IF/ICC Figures
IF Staining of HepG2 using 16386-1-AP (same clone as 16386-1-PBS)
Immunofluorescent analysis of HepG2 cells using 16386-1-AP (RPL23A antibody) at dilution of 1:50 and Alexa Fluor 488-conjugated AffiniPure Goat Anti-Rabbit IgG(H+L). This data was developed using the same antibody clone with 16386-1-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
RPL23A Polyclonal antibody
Catalog Number
16386-1-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
