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查看说明书Recombinant Human NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial (NDUFS2)
Cat#:TP03129应用：Positive Control; Immunogen; SDS-PAGE; WB
| Product Name: | NDUFS2 Recombinant Rabbit mAb |
| Cat No.: | RMA02118 |
| Clonality: | Monoclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB,IHC,IP |
| Recommended Dilution: | WB,IHC,IP |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | Recombinant protein of human NDUFS2 |
| Calculated Molecular Weight: | 53 kDa |
| Observed Molecular Weight: | 49 kDa |
| GenBank Accession Number: | O75306 |
| Gene ID (NCBI): | 4720 |
| Synonyms: | CI-49; MC1DN6 |
| Background: | 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.[provided by RefSeq, Oct 2009] |
| Category: | Primary Ab |
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