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D-dopachrome tautomerase converts D-dopachrome into 5,6-dihydroxyindole. Additionally we are shipping D-Dopachrome Tautomerase Kits (24) and D-Dopachrome Tautomerase Proteins (16) and many more products for this protein.
Showing 10 out of 77 products:
Cow (Bovine) Polyclonal DDT Primary Antibody for WB - ABIN2782455
Ewing, Chu, Elisma, Li, Taylor, Climie, McBroom-Cerajewski, Robinson, OConnor, Li, Taylor, Dharsee, Ho, Heilbut, Moore, Zhang, Ornatsky, Bukhman, Ethier, Sheng, Vasilescu, Abu-Farha, Lambert, Duewel et al.: Large-scale mapping of human protein-protein interactions by mass spectrometry. ... in Molecular systems biology 2007
Human Polyclonal DDT Primary Antibody for IHC (p), WB - ABIN5576493
Yoshihisa, Rehman, Kondo, Shimizu: Role of macrophage migration inhibitory factor in heat-induced apoptosis in keratinocytes. in FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2016
Human Monoclonal DDT Primary Antibody for ELISA, WB - ABIN560588
Hiyoshi, Konishi, Uemura, Matsuzaki, Tsukamoto, Sugimoto, Takeda, Dakeshita, Kitayama, Takami, Sawachika, Kido, Arisawa: D-Dopachrome tautomerase is a candidate for key proteins to protect the rat liver damaged by carbon tetrachloride. in Toxicology 2008
Study demonstrated that DDT was over- expressed in pancreatic ductal adenocarcinoma (PDAC) tissues and cell lines in a pattern correlated with MIF (show AMH Antibodies), and knockdown of DDT and MIF (show AMH Antibodies) in PANC- 1 cells cooperatively inhibited cell proliferation, invasion and tumor formation. The tautomerase activities of both MIF (show AMH Antibodies) and DDT are required for their negative regulatory role in p53 (show TP53 Antibodies) and their tumor-promoting functions.
DDT was increased in burn patients.
Gene expression level of DDT is significantly higher in AD patients when compared to normal controls.
High MIF-2 (show CENPC1 Antibodies) levels are predictive of the development of organ dysfunction in myocardial ischemia reperfusion injury.
Both p53 (show TP53 Antibodies) wildtype and mutant human lung adenocarcinoma tumors rely on MIF (show AMH Antibodies) family members for maximal cell growth and survival.
findings identify DDT as a functionally redundant but more potent cytokine to MIF (show AMH Antibodies) in cancer and suggest that current attempts to inhibit MIF (show AMH Antibodies) signaling may fail because of DDT compensation.
D-dopachrome tautomerase secreted from adipocytes acts on preadipocytes to promote IL-6 (show IL6 Antibodies) expression and to inhibit adipogenesis by suppressing the induction of genes encoding adipogenic regulators
DDT acts on adipocytes to regulate lipid metabolism through AMPK (show PRKAA1 Antibodies) and/or PKA pathway(s) and improves glucose intolerance caused by obesity.
These data indicate that D-DT is a MIF (show AMH Antibodies)-like cytokine.
D-DT-dependent beta-catenin (show CTNNB1 Antibodies) stabilization is regulated by COX-2 (show COX2 Antibodies) expression, suggesting the existence of an amplification loop between COX-2 (show COX2 Antibodies)- and beta-catenin (show CTNNB1 Antibodies)-mediated transcription in these cells
cardiomyocyte secretion of DDT has important autocrine/paracrine effects during ischemia-reperfusion that protect the heart against injury
These data point to a potential involvement of D-dopachrome tautomerase activity in the mature mouse brain, and suggest some functional and evolutionary relationship between innate immunity and tautomerization of D-dopachrome in mammalian species
These data indicate that D-DT is a MIF (show MIF Antibodies)-like cytokine.
D-dopachrome tautomerase converts D-dopachrome into 5,6-dihydroxyindole. The DDT gene is related to the migration inhibitory factor (MIF) in terms of sequence, enzyme activity, and gene structure. DDT and MIF are closely linked on chromosome 22.
, D-dopachrome decarboxylase-A
, D-dopachrome tautomerase-A
, D-dopachrome decarboxylase-B
, D-dopachrome tautomerase-B
, D-dopachrome tautomerase
, dopachrome isomerase
, phenylpyruvate tautomerase II