Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
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 anti-LC3B/MAP1LC3B antibody (PA01524). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human U2OS whole cell lysates,
Lane 2: human U87 whole cell lysates,
Lane 3: rat brain tissue lysates,
Lane 4: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-LC3B/MAP1LC3B antigen affinity purified polyclonal antibody (PA01524) 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 LC3B/MAP1LC3B at approximately 15,18 kDa. The expected band size for LC3B/MAP1LC3B is at 15 kDa.
IHC analysis of LC3B/MAP1LC3B using anti-LC3B/MAP1LC3B antibody (PA01524).
LC3B/MAP1LC3B was detected in a paraffin-embedded section of human glioma tissue. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of LC3B/MAP1LC3B using anti-LC3B/MAP1LC3B antibody (PA01524).
LC3B/MAP1LC3B was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of LC3B/MAP1LC3B using anti-LC3B/MAP1LC3B antibody (PA01524).
LC3B/MAP1LC3B was detected in a paraffin-embedded section of rat brain tissue. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
Western blot analysis of anti-LC3B/MAP1LC3B antibody (PA01524). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human U2OS whole cell lysates,
Lane 2: human U87 whole cell lysates,
Lane 3: rat brain tissue lysates,
Lane 4: mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-LC3B/MAP1LC3B antigen affinity purified polyclonal antibody (PA01524) 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 LC3B/MAP1LC3B at approximately 15,18 kDa. The expected band size for LC3B/MAP1LC3B is at 15 kDa.
IHC analysis of LC3B/MAP1LC3B using anti-LC3B/MAP1LC3B antibody (PA01524).
LC3B/MAP1LC3B was detected in a paraffin-embedded section of human glioma tissue. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of LC3B/MAP1LC3B using anti-LC3B/MAP1LC3B antibody (PA01524).
LC3B/MAP1LC3B was detected in a paraffin-embedded section of mouse brain tissue. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IHC analysis of LC3B/MAP1LC3B using anti-LC3B/MAP1LC3B antibody (PA01524).
LC3B/MAP1LC3B was detected in a paraffin-embedded section of rat brain tissue. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.