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AN301939L

Recombinant SLC25A12 Monoclonal Antibody

Größe

£252.90

War £281.00

SKU:
AN301939L
Zusätzliche Namen:
AGC,EIEE,SLC25A,SLC25A12,AGC1,ARALAR,EIEE39,ARALAR1,Araceli hiperlarga,Calcium binding mitochondrial carrier superfamily member,Calcium binding mitochondrial carrier superfamily member Aralar1,Calcium-binding mitochondrial carrier protein Aralar1,CMC1,member 12,Mitochondrial aspartate glutamate carrier 1,solute carrier family 25,Solute carrier family 25 (aspartate/glutamate carrier) member 12,Solute carrier family 25 (mitochondrial carrier Aralar) member 12,Solute carrier family 25 member 12
Anwendung:
IHC, WB
Konzentration:
1 mg/ml
Aufreinigung:
Protein A Purified
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles.
Hersteller:
Elabscience
Host:
Rabbit
Reaktivitäten:
Human, Mouse, Rat
Buffer:
PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Immunogen:
Recombinant human SLC25A12 fragment
Klon:
A655
Uniprot:
O75746
Synonyme:
AGC1;araceli hiperlarga;ARALAR;calcium binding mitochondrial carrier superfamily member Aralar1;calcium-binding mitochondrial carrier protein Aralar1;DEE39;EIEE39;mitochondrial aspartate glutamate carrier 1;solute carrier family 25 (aspartate/glutamate carrier), member 12;solute carrier family 25 (mitochondrial carrier, Aralar), member 12;Solute carrier family 25 member 12
Weitere Details:
The calcium-binding mitochondrial carrier protein (SLC25A12), also named as ARALAR or AGC1, is an aspartate-glutamate exchange protein responsible for transporting mitochondrial aspartate across the mitochondrial inner membrane in exchange for cytosolic glutamate. SLC25A12 and other proteins of the aspartate-glutamate carrier (AGC) group are required for the transfer of mitochondrial aspartate to the cytosol, a key step in urea synthesis. Research studies using SLC25A12-knockout mice indicate that SLC25A12 plays an important role in proper CNS myelination. Mice lacking SLC25A12 suffer from hypomyelination as a result of a lack of oligodendrocyte maturation caused by decreased brain N-acetylaspartate levels. Mutation of the corresponding SLC25A12 gene can result in global cerebral hypomyelination and severe psychomotor retardation, caused by deficient SLC25A12 activity and limited mitochondrial aspartate efflux.
Versandbedingungen:
Blue Ice