Background：This gene encodes a calcium-binding mitochondrial carrier protein. The encoded protein localizes to the mitochondria and is involved in the exchange of aspartate for glutamate across the inner mitochondrial membrane. Polymorphisms in this gene may be associated with autism, and mutations in this gene may also be a cause of global cerebral hypomyelination. Alternatively spliced transcript variants have been observed for this gene.
仕様
Synonyms：AGC1,Araceli hiperlarga,ARALAR,ARALAR1,Calcium binding mitochondrial carrier superfamily member,Calcium binding mitochondrial carrier superfamily member Aralar1,Calcium-binding mitochondrial carrier protein Aralar1,CMC1,Mitochondrial aspartate glutamate carrier 1,SLC25A12,Solute carrier family 25 （aspartate/glutamate carrier） member 12,Solute carrier family 25 （mitochondrial carrier Aralar） member 12,Solute carrier family 25 member 12,solute carrier family 25,member 12
Host：Rabbit
Reactivity：Human,Mouse
Applications：IHC,ELISA
Concentration：0.4mg/mL
Immunogen：Synthetic peptide of human SLC25A12
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：PBS with 0.05％ sodium azide, 50％ glycerol, PH7.3
Dilution：IHC 1：25-1：100
Swissprot：O75746
Isotype：IgG
Research Areas：Cancer, Metabolism, Neuroscience, Signal transduction, Tags ＆ Cell Markers
