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Slc25a12 encodes a calcium-binding mitochondrial carrier protein. Additionally we are shipping Solute Carrier Family 25 (Mitochondrial Carrier, Aralar), Member 12 Kits (4) and Solute Carrier Family 25 (Mitochondrial Carrier, Aralar), Member 12 Proteins (3) and many more products for this protein.
Showing 10 out of 51 products:
Cow (Bovine) Polyclonal Slc25a12 Primary Antibody for WB - ABIN2781595
Silverman, Buxbaum, Ramoz, Schmeidler, Reichenberg, Hollander, Angelo, Smith, Kryzak: Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism. in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008
Human Monoclonal Slc25a12 Primary Antibody for IF, WB - ABIN968399
del Arco, Satrústegui: Molecular cloning of Aralar, a new member of the mitochondrial carrier superfamily that binds calcium and is present in human muscle and brain. in The Journal of biological chemistry 1998
rs2056202 and rs2292813 in SLC25A12 may contribute significantly to autism spectrum disorders risk.
Compares and contrasts all the known human SLC25A (show SLC25A25 Antibodies)* genes and includes functional information.
The physiological roles of AGC1 (show ACAN Antibodies), its links to calcium homeostasis, and its involvement in autism pathogenesis, are reviewed.
Variants of the AGC1 (show ACAN Antibodies)-encoding SLC25A12 gene were neither correlated with AGC (show ACAN Antibodies) activation nor associated with autism-spectrum disorders in 309 simplex and 17 multiplex families.
SLC25A12 gene is linked to autism
Aralar1 has a role in determining glucose metabolic fate, mitochondrial activity, and insulin (show INS Antibodies) secretion in beta cells
These results suggest that SLC25A12 is not a major contributor to autism risk in these families.
it is unlikely that the SLC25A12 polymorphisms investigated play a substantial role in conferring susceptibility to schizophrenia
rs2056202 polymorphism in SLC25A12 may be associated with levels of routines and rituals in autism and related disorders
SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects.
Muller glia compensate for their unique metabolic adaptations by using lactate and aspartate from neurons as surrogates for their missing PK and AGC1 (show ACAN Antibodies).
Aralar (show slc25a13 Antibodies) protein & mRNA expressions were the same in adult neurons & astrocytes, whole brain,& well-differentiated astrocyte cultures, but not until late development, like the late-maturing brain ability to form & degrade glutamate (show GRIN1 Antibodies).
Aralar (show slc25a13 Antibodies)-knockout postnatal mice show hyperactivity, anxiety-like behavior, and hyperreactivity with a decrease of dopamine (DA) in terminal-rich regions.
Postnatal Electrophysiological Development Is Arrested in Aralar (show slc25a13 Antibodies)-Knockout Mice.
Aralar1 was clearly separated, unambiguously identified and characterized from protein extracts of mouse hippocampus by the use of the multidimensional gel electrophoretic steps.
Slc25a12-knockout mice, which showed no AGC1 (show ACAN Antibodies) by immunoblotting but displayed delayed development and died around 3 weeks after birth. In postnatal day 13 to 14 knockout brains, the brains were smaller with no obvious alteration in gross structure.
Expression of the aspartate/glutamate (show GRIN1 Antibodies) mitochondrial carriers aralar1 and citrin (show slc25a13 Antibodies) during development
These results show that aralar (show slc25a13 Antibodies) plays an important role in myelin formation by providing aspartate for the synthesis of N-acetylaspartate in neuronal cells.
aralar (show slc25a13 Antibodies) has an essential role in the transduction of small Ca2 (show CA2 Antibodies)+ signals to neuronal mitochondria
Aralar (show slc25a13 Antibodies) and citrin (show slc25a13 Antibodies), when expressed as single isoforms in heart, confer differences in Ca(2 (show CA2 Antibodies)+) activation of shuttle activity, probably associated with their structural differences.
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.
calcium-binding mitochondrial carrier protein Aralar1
, solute carrier family 25 (mitochondrial carrier, Aralar), member 12
, mitochondrial solute carrier family 25 member 12
, araceli hiperlarga
, calcium binding mitochondrial carrier superfamily member Aralar1
, mitochondrial aspartate glutamate carrier 1
, solute carrier family 25, member 12
, solute carrier family 25 member 12