slc25a13 anticorps (AA 248-505)

N° du produit ABIN1886262

Détail du produit anti-slc25a13 anticorps

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

Épitope: AA 248-505

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp slc25a13 est non-conjugé

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

Purification: Purified by antigen-affinity chromatography.

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

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.50-1.500

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

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

Détails sur slc25a13

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

Autre désignation: SLC25A13 (slc25a13 Produits)

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

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.[provided by RefSeq]

Poids moléculaire: 74 kDa

ID gène: 10165

NCBI Accession: NM_014251, NP_055066

Pathways: Ribonucleoside Biosynthetic Process, Dicarboxylic Acid Transport