Background:  Macrophage migration inhibitory factor, known as MIF or glycosylation-inhibiting factor, is a secreted, homotrimeric, pro-inflammatory cytokine that modulates macrophage and T cell function and is an important regulator of host response to infection. MIF is expressed at sites of inflammation, which suggests that it plays a role in regulating macrophage function in host defense. The only known family member of MIF is D-dopachrome tautomerase (DDT), a protein that is thought to similarly play a role in the inflammation process. DDT is highly expressed in liver with lower levels in other organs, including heart, lung and pancreas. It resides in the cytoplasm as a homotrimer and converts 2-carboxy-2,3-dihyroindole-5, 6-quinone (D-dopachrome) into 5,6-dihydroxyindole. DDT requires the presence of an N-terminal proline residue for catalytic activity and is involved in the biosynthesis of melanin, an antioxidant. In response to liver damage, DDT has been shown to increase protein levels in order to accelerate melanin biosynthesis and protect the liver from oxidative stress.

Description: Rabbit polyclonal to DDT

Immunogen: KLH conjugated synthetic peptide derived from DDT

Specificity:  ·Reacts with Human, Mouse, Pig and Rat.

·Isotype: IgG

Application:  ·Western blotting: 1/100-500. Predicted Mol wt: 13 kDa;

·Immunohistochemistry (Paraffin/frozen tissue section): 1/50-200;

·Immunocytochemistry/Immunofluorescence: 1/100;

·Immunoprecipitation: 1/50;

·ELISA: 1/500;

·Optimal working dilutions must be determined by the end user.