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AASS encodes a bifunctional enzyme that catalyzes the first two steps in the mammalian lysine degradation pathway. De plus, nous expédions Aminoadipate Semialdehyde Synthase Anticorps (38) et Aminoadipate Semialdehyde Synthase Protéines (4) et beaucoup plus de produits pour cette protéine.
GR and KLF15 (Montrer KLF15 Kits ELISA) physically interact via low affinity GR binding sites within glucocorticoid response elements (GREs) for PRODH (Montrer PRODH Kits ELISA) and AASS that contribute to combinatorial regulation with KLF15 (Montrer KLF15 Kits ELISA).
Mitochondrial NADPH (Montrer NQO1 Kits ELISA) is crucial for AASS function
Hyperlysinemia is caused by mutations in AASS
These results indicate AASS knockdown decreases the lysine requirement of the cell via a reduction of lysine catabolism through the saccharopine pathway.
Mice receiving the high-protein diet had greater AASS mRNA compared to mice fed the adequate protein diet.
This gene encodes a bifunctional enzyme that catalyzes the first two steps in the mammalian lysine degradation pathway. The N-terminal and the C-terminal portions of this enzyme contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha-aminoadipic semialdehyde. Mutations in this gene are associated with familial hyperlysinemia.
alpha-aminoadipate semialdehyde synthase
, alpha-aminoadipic semialdehyde synthase, mitochondrial
, aminoadipic semialdehyde synthase
, lysine-2-oxoglutarate reductase
, lysine-ketoglutarate reductase /saccharopine dehydrogenase
, lysine oxoglutarate reductase
, saccharopine dehydrogenase