slc25a13 antibody (AA 1-643)

Catalog No. ABIN7869514

The Rabbit Polyclonal anti-slc25a13 antibody (ABIN7869514) specifically detects slc25a13 in WB, ELISA, IF, IHC (p) and FACS. The antibody is reactive with Human and Rat samples.

Quick Overview for slc25a13 antibody (AA 1-643) (ABIN7869514)

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

Reactivity: Human, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This slc25a13 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)

Product Details anti-slc25a13 Antibody

Binding Specificity: AA 1-643

Purpose: Citrin Antibody / ARALAR2 / SLC25A13

Purification: Antigen affinity purified

Immunogen: E. coli-derived recombinant human protein (amino acids M1-A643) was used as the immunogen for the Citrin antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the Citrin antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the Citrin antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details for slc25a13

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

Alternative Name: Citrin

Background: Citrin also known as solute carrier family 25, member 13 (also called Citrin and ARALAR-related gene 2) is a protein which in humans is encoded by the SLC25A13 gene. 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.

UniProt: Q9UJS0

Pathways: Ribonucleoside Biosynthetic Process, Dicarboxylic Acid Transport