slc25a13 Protein (His tag)
-
- Antigène Voir toutes slc25a13 Protéines
- slc25a13 (Solute Carrier Family 25, Member 13 (Citrin) (slc25a13))
- Type de proteíne
- Recombinant
-
Origine
- Humain
-
Source
- Escherichia coli (E. coli)
- Purification/Conjugué
- Cette slc25a13 protéine est marqué à la His tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
-
- Recombinant human SLC25A13 / Citrin (full length, N-term HIS tag, transcript variant 2) protein expressed in E.coli.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product slc25a13 Protéine
-
-
- Indications d'application
-
Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
-
The tag is located at the N-terminal.
- Restrictions
- For Research Use only
-
- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
- Stock
- -80 °C
- Stockage commentaire
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
-
- Antigène
- slc25a13 (Solute Carrier Family 25, Member 13 (Citrin) (slc25a13))
- Autre désignation
- Slc25a13,citrin (slc25a13 Produits)
- Synonymes
- MGC69168 Protein, ctln2 Protein, citrin Protein, aralar2 Protein, AI785475 Protein, Ctrn Protein, ARALAR2 Protein, CITRIN Protein, CTLN2 Protein, RGD1565889 Protein, solute carrier family 25 member 13 L homeolog Protein, solute carrier family 25 member 13 Protein, solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 Protein, slc25a13.L Protein, SLC25A13 Protein, slc25a13 Protein, Slc25a13 Protein
- Sujet
- 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.
- Poids moléculaire
- 74 kDa
- NCBI Accession
- NP_055066
- Pathways
- Ribonucleoside Biosynthetic Process, Dicarboxylic Acid Transport
-