The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Use a concentration of 5 µg/ml.
Use a concentration of 1 µg/ml. Predicted molecular weight: 34 kDa.
Use a concentration of 0.5 - 1 µg/ml.
Use at an assay dependent concentration.
Molecular scaffold protein for various multimeric protein complexes. Acts as a module in the assembly of a multicomponent scaffold for the ERK pathway, linking ERK responses to specific agonists. At low concentrations it enhances ERK activation, whereas high concentrations lead to the inhibition of ERK activation. Also involved in response to hypoxia by acting as a negative regulator of HIF1A/HIF-1-alpha via its interaction with EGLN3/PHD3. May promote degradation of HIF1A. May act by recruiting signaling complexes to a specific upstream activator (By similarity). May also be involved in pre-mRNA splicing.
Belongs to the WD repeat MORG1 family. Contains 7 WD repeats.
This image shows human mammary cancer tissue stained with ab65870 at 1µg/ml. Cytoplasmic staining of Morg1, using DAB.
Western blot - Anti-Morg1 antibody - Aminoterminal end (ab65870)
Anti-Morg1 antibody - Aminoterminal end (ab65870) at 1 µg/ml + rat brain tissue lysate
Predicted band size: 34 kDa Observed band size: 34 kDa
Immunocytochemistry/ Immunofluorescence - Anti-Morg1 antibody - Aminoterminal end (ab65870)
ICC/IF image of ab65870 stained HepG2 cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab65870, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.