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SLC25A24 encodes a carrier protein that transports ATP-Mg exchanging it for phosphate. Additionally we are shipping SLC25A24 Antibodies (28) and many more products for this protein.
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The SLC25A24 mutations induce a gain of pathological function.
The SLC25A24 mutations lead to impaired mitochondrial ATP synthesis.
Genetic analyses in human and mouse models revealed the importance of SLC25A24/Slc25a24 in the regulation of body fat mass and adipogenesis.
N-terminal EF hands form a self-sequestered compact calmodulin like Ca-sensor in the presence of Ca2+
Compares and contrasts all the known human SLC25A* genes and includes functional information.
SCaMC-1 is the human orthologue of the rabbit Efinal protein, which was reported to be located in peroxisomes
identification of three isoforms of the mitochondrial ATP-Mg/Pi carrier APC1, APC2 and APC3; they are most likely responsible for the net uptake or efflux of adenine nucleotides into or from the mitochondria
This gene encodes a carrier protein that transports ATP-Mg exchanging it for phosphate. Multiple transcript variants encoding different isoforms have been found for this gene.
calcium-binding mitochondrial carrier protein SCaMC-1
, small calcium-binding mitochondrial carrier protein 1
, solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 24
, solute carrier family 25 member 24
, calcium-binding mitochondrial carrier protein SCaMC-1-A
, small calcium-binding mitochondrial carrier protein 1-A
, solute carrier family 25 member 24-A
, calcium-binding transporter
, mitochondrial ATP-Mg/Pi carrier protein 1
, mitochondrial Ca(2+)-dependent solute carrier protein 1
, short calcium-binding mitochondrial carrier 1
, peroxisomal Ca(2+)-dependent solute carrier
, peroxisomal Ca-dependent solute carrier