Alanyl-tRNA Synthetase Domain Containing 1 (AARSD1) Antibody (HRP)
169€ (20 µg)
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Name
Alanyl-tRNA Synthetase Domain Containing 1 (AARSD1) Antibody (HRP)
Category
Primary Antibodies
Provider
Abbexa
Reference
abx310714
Tested Applications
ELISA
Description
AARSD1 Antibody (HRP) is a Rabbit Polyclonal against AARSD1 conjugated to HRP.
Documentos del producto
Instrucciones
Data sheet
Especificaciones del producto
| Category | Primary Antibodies |
| Immunogen Target | Target: Alanyl-tRNA Synthetase Domain Containing 1 (AARSD1) Immunogen: Recombinant human Alanyl-tRNA editing protein Aarsd1 protein (1-230AA). |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | HRP |
| Isotype | IgG |
| Purity | > 95% |
| Purification | Purified by Protein G. |
| Size 1 | 20 µg |
| Size 2 | 50 µg |
| Size 3 | 100 µg |
| Size 4 | 200 µg |
| Size 5 | 1 mg |
| Form | Liquid |
| Tested Applications | ELISA |
| Buffer | 0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% Glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid exposure to light. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q9BTE6 |
| Gene ID | 100885850, 80755 |
| NCBI Accession | NP_001129514.2, NM_001136042.2, NP_001248363.1, NM_001261434.1 |
| Alias | AlaXp |
| Background | Antibody anti-AARSD1 |
| Status | RUO |
| Note | THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION. |
Background
Alanyl-tRNA Synthetase Domain Containing 1 (AARSD1) is a mitochondrial protein involved in the synthesis of alanyl-tRNA, which is essential for the translation of mitochondrial-encoded proteins. It catalyzes the attachment of alanine to its corresponding tRNA, ensuring proper protein synthesis for mitochondrial function and energy production. AARSD1 is critical for mitochondrial biogenesis and oxidative phosphorylation, and mutations in the AARSD1 gene can lead to mitochondrial dysfunction, resulting in metabolic disorders, neurodegenerative diseases, or myopathies. Emerging studies suggest that AARSD1 also plays a role in cellular stress responses and may influence processes such as apoptosis and adaptive mitochondrial dynamics.
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