slc25a13 antibody (AA 248-505)

Catalog No. ABIN1886262

Product Details anti-slc25a13 Antibody

Target: slc25a13 (Solute Carrier Family 25, Member 13 (Citrin) (slc25a13))

Binding Specificity: AA 248-505

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This slc25a13 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 248 and 505 of Human SLC25A13

Application Details

Application Notes: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.50-1.500

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Preservative: Thimerosal (Merthiolate)

Precaution of Use: Biohazard Informations: This product contains thimerosal which is hazardous.

Storage: 4 °C/-20 °C

Storage Comment: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Target Details for slc25a13

Target: slc25a13 (Solute Carrier Family 25, Member 13 (Citrin) (slc25a13))

Alternative Name: SLC25A13 (slc25a13 Products)

Synonyms: MGC69168 antibody, ctln2 antibody, citrin antibody, aralar2 antibody, AI785475 antibody, Ctrn antibody, ARALAR2 antibody, CITRIN antibody, CTLN2 antibody, RGD1565889 antibody, solute carrier family 25 member 13 L homeolog antibody, solute carrier family 25 member 13 antibody, solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 antibody, slc25a13.L antibody, SLC25A13 antibody, slc25a13 antibody, Slc25a13 antibody

Background: 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]

Molecular Weight: 74 kDa

Gene ID: 10165

NCBI Accession: NM_014251, NP_055066

Pathways: Ribonucleoside Biosynthetic Process, Dicarboxylic Acid Transport