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查看说明书Recombinant Human NDUFB9 Protein
Cat#:TP03128应用：Positive Control; Immunogen; SDS-PAGE; WB
| Product Name: | NDUFB9 Recombinant Rabbit mAb |
| Cat No.: | RMA01439 |
| Clonality: | Monoclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB,IHC,ICC/IF,FC,IP |
| Recommended Dilution: | WB,IHC,ICC/IF,FC,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 NDUFB9 |
| Calculated Molecular Weight: | 22 kDa |
| Observed Molecular Weight: | 22 kDa |
| GenBank Accession Number: | Q9Y6M9 |
| Gene ID (NCBI): | 4715 |
| Synonyms: | B22; LYRM3; CI-B22; UQOR22 |
| Background: | The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015] |
| Category: | Primary Ab |
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