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SLC7A3 encodes a member of the solute carrier family 7. De plus, nous expédions SLC7A3 Anticorps (17) et et beaucoup plus de produits pour cette protéine.
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null mutants have hepatic steatosis
rare hypomorphic variants of SLC7A3 exist in male individuals, SLC7A3 variants possibly contribute to the etiology of autism spectrum disorders in male subjects in association with other genetic factors
knockdown impaired AMPK-PPAR-alpha signaling and resulted in lipid accumulation under glucose starvation in liver cells
CAT1, CAT2, and CAT3 localized in adult brains but with uneven distribution.
is concluded that hCAT-3 is a passive transport system that conducts monovalent cations including L-Arg.
It is concluded that similar to hCAT-1, hCAT-3 activity is decreased by PKC via reduction of transporter molecules in the plasma membrane.
knockdown impaired AMPK-PPAR-alpha signaling and resulted in lipid accumulation under fasting
In a neuronal cell model, y+,L and y+ transport systems are the predominant form of arginine uptake mechanisms and the transport of arginine is altered by membrane potential and redox factors.
This gene encodes a member of the solute carrier family 7. The encoded protein is a sodium-independent cationic amino acid transporter. Alternate splicing results in multiple transcripts that encoded the same protein.
solute carrier family 7 (cationic amino acid transporter, y+ system), member 3
, solute carrier family 7, member 3
, cationic amino acid transporter 3-like
, cationic amino acid transporter 3
, amino acid transporter, cationic 3
, cationic amino acid transporter y+
, solute carrier family 7 member 3