Succinate Dehydrogenase Complex Subunit A (SDHA) Antibody (Biotin)
169€ (20 µg)
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935106861
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name
Succinate Dehydrogenase Complex Subunit A (SDHA) Antibody (Biotin)
category
Primary Antibodies
provider
Abbexa
reference
abx105945
tested applications
ELISA
Description
Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial Antibody (Biotin) is a Rabbit Polyclonal antibody against Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial conjugated to Biotin.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Target: Succinate Dehydrogenase Complex Subunit A (SDHA) Immunogen: Recombinant human Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial protein (44-664AA). |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Biotin |
| 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 | P31040 |
| Gene ID | 6389 |
| NCBI Accession | NP_001281261.1, NM_001294332.1 |
| OMIM | 252011 |
| Background | Antibody anti-SDHA |
| 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. |
Descripción
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This gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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