CMC2 Polyclonal Antibody
Sizes: 50μL, 100μL
Catalogue Numbers: RA31698-50, RA31698-100
Citations, Manuals and MSDS Available upon request.
Background: solute carrier family 25 member 13 (SLC25A13) Homo sapiens 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. [provided by RefSeq, May 2009],
Condition: Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Storage Instructions: -20°C/1 year
Recommended dilutions: WB 1:500-2000 ELISA 1:5000-20000
Applications: WB; ELISA
Species Cross-Reactivity: Human; Mouse
GeneID (Human): 10165
Protein MW (KDa): 74
SWISS: Q9UJS0
Source: Rabbit
Research Use Only