SLC25A13 antibody
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935106861
info@markelab.com
name
SLC25A13 antibody
category
Primary Antibodies
provider
FineTest
reference
FNab07930
tested applications
ELISA, WB, IHC, IF
Description
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.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | solute carrier family 25, member 13 (citrin) (SLC25A13) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | WB: 1:500 - 1:2000; IHC: 1:50 - 1:200; IF: 1:50 - 1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 74 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IHC, IF |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.) |
| UniProt ID | Q9UJS0 |
| Gene ID | 10165 |
| Alias | Electrogenic aspartate/glutamate antiporter SLC25A13, mitochondrial,Calcium-binding mitochondrial carrier protein Aralar2 (ARALAR-related gene 2, ARALAR2),Citrin,Mitochondrial aspartate glutamate carrier 2,Solute carrier family 25 member 13,SLC25A13 |
| Background | Antibody anti-SLC25A13 |
| Status | RUO |
| Note | Mol. Weight 74 kDa |
Descripción
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Human SLC25A13 (Calcium-binding mitochondrial carrier protein Aralar2) ELISA Kit
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SLC25A13 antibody
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.
Ver Producto