Western Blot
Positive WB detected in: Hela whole cell lysate, Jurkat whole cell lysate, MCF-7 whole cell lysate, K562 whole cell lysate, SH-SY5Y whole cell lysate
All lanes: MAG antibody at 4.2ug/ml
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 70,64,67 KDa
Observed band size: 70 KDa
Immunofluorescence staining of MCF-7 cells with MBS1490028 at 1:416,counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4 degree C.The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG (H+L).
Western Blot
Positive WB detected in: SH-SY5Y whole cell
lysate, Rat brain tissue
All lanes:MAG antibody at 5mg/ml
Secondary Goat polyclonal to
rabbit IgG at 1/50000 dilution
Predicted band size: 70, 64, 67 kDa
Observed band size: 70, 100 kDa
IHC image of MBS1490028 diluted at1:600 and staining in paraffin-embedded humankidney tissue performed on a Leica BondTMsystem. After dewaxing and hydration, antigen retrieval was mediated by high pressure in acitrate buffer (pH 6.0). Section was blocked with10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at4°C overnight. The primary is detected by abiotinylated secondary antibody and visualizedtissue using an HRP conjugated SP system.
IHC image of MBS1490028 diluted at1:600 and staining in paraffin-embedded humanbrain tissue performed on a Leica BondTMsystem. After dewaxing and hydration, antigenretrieval was mediated by high pressure in acitrate buffer (pH 6.0). Section was blocked with10% normal goat serum 30min at RT. Thenprimary antibody (1% BSA) was incubated at4°C overnight. The primary is detected by abiotinylated secondary antibody and visualizedtissue using an HRP conjugated SP system