Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Zusätzlich bieten wir Ihnen Histidine Ammonia-Lyase Antikörper (27) und Histidine Ammonia-Lyase Proteine (5) und viele weitere Produktgruppen zu diesem Protein an.
Showing 4 out of 8 products:
photoprotective role of endogenous urocanic acid in the murine skin using histidinemic mice, in which the gene encoding histidase is mutated
Three LoF mutations in HAL were associated with increased histidine levels, which in turn were shown to be inversely related to the risk of CHD (zeige CHDH ELISA Kits) among both African Americans and European Americans.
This evidence supports that the Hal gene is turned on by glucocorticoids and by glucagon either via PKC or PKA, but prefers the PKA pathway.
This report describes the first mutations occurring in the coding region of the histidase structural gene in patients with histidinemia.
histidase is upregulated during keratinocyte differentiation and that all-trans retinoic acid but not UV irradiation modulates the expression level
SNPs within the HAL gene are associated with milk production traits in Chinese Holstein cows.
Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids. Several transcript variants encoding different isoforms have been found for this gene.
, histidine ammonia lyase