The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Use a concentration of 0.3 - 1 µg/ml.
Use a concentration of 3 - 5 µg/ml. Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
Most of the commercially available BSA and dry milk are contaminated with bovine IgG (even some of the higher purity grades of BSA); this might cause high background problems when labelled anti-goat secondary is used. The secondary might cross-react with bovine IgG since goat is closely related to cow.
Dual specificity phosphatase that dephosphorylates MAP kinase ERK2 on both 'Thr-183' and 'Tyr-185'.
Expressed at high levels in the lung, liver placenta and pancreas. Moderate levels seen in the heart and skeletal muscle. Lower levels found in the brain and kidney.
Belongs to the protein-tyrosine phosphatase family. Non-receptor class dual specificity subfamily. Contains 1 rhodanese domain. Contains 1 tyrosine-protein phosphatase domain.
Dual specificity protein phosphatase hVH1 antibody
DUSP 1 antibody
MAP kinase phosphatase 1 antibody
Mitogen-activated protein kinase phosphatase 1 antibody
Protein tyrosine phosphatase CL100 antibody
Protein-tyrosine phosphatase CL100 antibody
Serine/threonine specific protein phosphatase antibody
Western blot - Anti-DUSP1 antibody (ab1351)
Endogenous DUSP1 staining (2µg/ml) of HeLa lysate (RIPA buffer, 35µg total protein per lane).Primary incubated for 1 hour.Detected by western blot using chemiluminescence Endogenous DUSP1 staining (2µg/ml) of HeLa lysate (RIPA buffer, 35µg total protein per lane). Primary incubated for 1 hour. Detected by western blot using chemiluminescence