SLC25A13 Antilichaam

This gene is a member of the mitochondrial carrier family. The encoded protein contains four EF-hand Ca (2+) binding motifs in the N-terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene.

10165

Q9UJS0

Human

Recombinant fusion protein containing a sequence corresponding to amino acids 1-300 of human SLC25A13 (NP_001153682.1) .

Unconjugated

Primary Antibodies

Other

Affinity purification

MCF7

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 74kDa

IgG

SLC25A13

SW480

HepG2

HeLa

Solute carrier family 25 member 13

Homo sapiens

ARALAR2, CITRIN, CTLN2, calcium-binding mitochondrial carrier protein Aralar2, mitochondrial aspartate glutamate carrier 2, solute carrier family 25 (aspartate/glutamate carrier), member 13

WB, IHC, IF

Liquid