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021-54845833/15800441009
中文名称：小鼠抗NDUFB9单克隆抗体
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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. |
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Applications: |
WB, IHC, FC |
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Name of antibody: |
NDUFB9 |
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Immunogen: |
Fusion protein of human NDUFB9 |
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Full name: |
NADH:ubiquinone oxidoreductase subunit B9 (NDUFB9), transcript variant 1 |
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Synonyms: |
B22; CI-B22; LYRM3; UQOR22 |
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SwissProt: |
Q9Y6M9 |
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IHC positive control: |
human kidney tissue and carcinoma of human liver tissue |
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IHC Recommend dilution: |
30-150 |
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WB Predicted band size: |
22 kDa |
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WB Positive control: |
HepG2, Hela, A549, COS7, Jurkat, MCF-7 cell lysates |
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WB Recommended dilution: |
500-2000 |
