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Mitochondrial carriers, including SLC25A26, are a family of transport proteins found mostly in the inner membranes of mitochondria. Additionally we are shipping and many more products for this protein.
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SLC25A26 mutations cause various mitochondrial defects, including those affecting RNA stability, protein modification, mitochondrial translation, and the biosynthesis of CoQ10 and lipoic acid.
Compares and contrasts all the known human SLC25A (show SLC25A25 Antibodies)* genes and includes functional information.
SAMC was expressed in mitochondria of all human tissues examined. The role of SAMC is probably to exchange cytosolic SAM (show TTN Antibodies) for mitochondrial S-adenosylhomocysteine. This is the 1st report of identification & characterization of the human SAMC & its gene.
Mitochondrial carriers, including SLC25A26, are a family of transport proteins found mostly in the inner membranes of mitochondria. They shuttle metabolites and cofactors through the mitochondrial membrane (Agrimi et al., 2004
S-adenosylmethionine mitochondrial carrier protein
, mitochondrial S-adenosylmethionine transporter
, solute carrier family 25 member 26
, solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 26
, solute carrier family 25, member 26