Anti-NDUFS2 antibody
Specifications
| Product Cat#: | AB-06-4911 |
| Product type: | Primary antibody |
| Antigen: | NDUFS2 |
| Immunogen: | Recombinant protein within human NDUFS2 aa 264-463/463. |
| Species immunized: | Rabbit |
| Isotype: | IgG |
| Applications: | Western Blot (1:400); Immunohistochemistry-Paraffin (1:100) |
| Reactivity: | Human, Rat, Mouse |
| Clonality (clone number): | Monoclonal, JE65-29 |
| Form: | Liquid |
| Buffer: | 1*TBS buffer (pH7.4), 0.05% BSA, 40% Glycerol, 0.05% NaN3. |
| Concentration: | 1 mg/ml |
| Purity: | Protein A affinity purified. |
| Storage: | Aliquot and freeze at -20°C. Avoid multiple freeze/thaw cycles. |
| Conjugate: | Unconjugated |
| Alternative names: | CI 49 antibody |
| CI 49kD antibody | |
| CI-49kD antibody | |
| Complex 1, mitochondrial respiratory chain, 49 KD subunit antibody | |
| Complex I 49kD antibody | |
| Complex I 49kDa subunit antibody | |
| Complex I-49kD antibody | |
| Mitochondrial antibody | |
| NADH dehydrogenase (ubiquinone) Fe S protein 2 49kDa antibody | |
| NADH dehydrogenase (ubiquinone) Fe S protein 2, 49kDa (NADH coenzyme Q reductase) antibody | |
| NADH dehydrogenase [ubiquinone] iron sulfur protein 2, mitochondrial antibody | |
| NADH dehydrogenase [ubiquinone] iron-sulfur protein 2 antibody | |
| NADH ubiquinone oxidoreductase 49 kDa subunit antibody | |
| NADH ubiquinone oxidoreductase NDUFS2 subunit antibody | |
| NADH-ubiquinone oxidoreductase 49 kDa subunit antibody | |
| NADH:ubiquinone oxidoreductase core subunit S2 antibody | |
| Ndufs2 antibody | |
| NDUS2_HUMAN antibody |
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Target information
The protein encoded by this gene is a core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I). Mammalian mitochondrial complex I is composed of at least 43 different subunits, 7 of which are encoded by the mitochondrial genome, and the rest are the products of nuclear genes. The iron-sulfur protein fraction of complex I is made up of 7 subunits, including this gene product. Complex I catalyzes the NADH oxidation with concomitant ubiquinone reduction and proton ejection out of the mitochondria. Mutations in this gene are associated with mitochondrial complex I deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Provider
Erpantech Laboratory
